1 research outputs found
Inter-model comparison of global hydroxyl radical (OH) distributions and their impact on atmospheric methane over the 2000â2016 period
The modeling study presented here aims to estimate
how uncertainties in global hydroxyl radical (OH) distributions, variability, and trends may contribute to resolving discrepancies between simulated and observed methane (CH4) changes since 2000. A multi-model ensemble of 14 OH fields was analyzed and aggregated into 64 scenarios
to force the offline atmospheric chemistry transport model
LMDz (Laboratoire de Meteorologie Dynamique) with a
standard CH4 emission scenario over the period 2000â2016.
The multi-model simulated global volume-weighted tropospheric mean OH concentration ([OH]) averaged over 2000â2010 ranges between 8:7*10^5 and 12:8*10^5 molec cm-3.
The inter-model differences in tropospheric OH burden and
vertical distributions are mainly determined by the differences in the nitrogen oxide (NO) distributions, while the spatial discrepancies between OH fields are mostly due to differences in natural emissions and volatile organic compound (VOC) chemistry. From 2000 to 2010, most simulated OH fields show an increase of 0.1â0:3*10^5 molec cm-3 in the tropospheric mean [OH], with year-to-year variations much smaller than during the historical period 1960â2000. Once
ingested into the LMDz model, these OH changes translated
into a 5 to 15 ppbv reduction in the CH4 mixing ratio
in 2010, which represents 7%â20% of the model-simulated
CH4 increase due to surface emissions. Between 2010 and
2016, the ensemble of simulations showed that OH changes
could lead to a CH4 mixing ratio uncertainty of > 30 ppbv.
Over the full 2000â2016 time period, using a common stateof-
the-art but nonoptimized emission scenario, the impact
of [OH] changes tested here can explain up to 54% of the
gap between model simulations and observations. This result
emphasizes the importance of better representing OH abundance and variations in CH4 forward simulations and emission optimizations performed by atmospheric inversions