EGU23-6649
https://doi.org/10.5194/egusphere-egu23-6649
EGU General Assembly 2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.

The seasonal cycles of land biosphere N2O fluxes and atmospheric N2O

Qing Sun1,2, Sebastian Lienert1,2, and Fortunat Joos1,2
Qing Sun et al.
  • 1Climate and Environmental Physics, University of Bern, Bern Switzerland
  • 2Oeschger Centre for Climate Change Research, University of Bern, Bern, Switzerland

Nitrous oxide (N2O) is a greenhouse gas and ozone-depleting agent that is predominately emitted from the land biosphere, linking to the yet only poorly understood carbon-nitrogen cycle. The seasonal cycle of the tropospheric N2O mixing ratio (aN2O), measured at globally distributed air sampling sites, offers an observational model constraint. Recent studies attribute the aN2O seasonality to exchange with N2O-depleted stratospheric air. Yet, how land biosphere N2O fluxes contribute to the seasonal amplitude, phasing, and amplitude growth of aN2O has not been well understood at global scales.

Here we apply surface-atmosphere fluxes from global simulations of the Nitrogen/N2O Model Inter-comparison Project (NMIP) and the Bern3D ocean model to atmospheric transport matrices to simulate aN2O at air sampling sites. Land N2O fluxes from eight NMIP models show broad agreement on seasonal phasing. In contrast, seasonal amplitudes of regionally averaged fluxes differ severalfold across models. For example, seasonal amplitudes range from 2.2 to 5.4 TgN yr­-1 (median: 3.7) for 20oN-40oN and from 1.1 to 4.5 TgN yr­-1 (2.3) for 40oN-60oN during 2001 to 2020. The amplitudes for these two regions increased on average by 155% and 84%, respectively, over the industrial period. The increase predominantly results from anthropogenic activities, e.g, fertilizer application. The seasonal amplitude of regional ocean-atmosphere fluxes (0.2 to 1.1 TgN yr-1) and their changes are comparably small.

The NMIP land fluxes result in seasonal amplitudes of aN2O on average ranging from 0.27 to 0.84 ppb (observed: 0.23 to 0.91 ppb) at six selected stations (Alert and Barrow, Ascension Island, Ragged Point, and Samoa, and Cape Grim). The model spread in aN2O amplitude is up to 0.55 ppb and, thus, large in comparison with observations. The contributions from Bern3D ocean fluxes to aN2O seasonality at the six stations (0.13 to 0.26 ppb) are generally smaller than from land. Substantial data-model mismatches in aN2O seasonal amplitudes and phasing are likely due to neglecting stratospheric fluxes in our models.

Our results demonstrate significant contributions of land biosphere N2O emissions to aN2O seasonality. Model uncertainties in land biosphere fluxes translate into large uncertainties in aN2O seasonality, calling for land biosphere model improvements. In situ aN2O observations, in combination with atmospheric transport and chemistry models, potentially provide a novel top-down constraint for global land biosphere models towards improved projections of C-N coupling, the land carbon sink, and atmospheric CO2 and N2O.

How to cite: Sun, Q., Lienert, S., and Joos, F.: The seasonal cycles of land biosphere N2O fluxes and atmospheric N2O, EGU General Assembly 2023, Vienna, Austria, 24–28 Apr 2023, EGU23-6649, https://doi.org/10.5194/egusphere-egu23-6649, 2023.