Search for: All records

Storylines of atmospheric circulation change, or physically self-consistent narratives of plausible future events, have recently been proposed as a non-probabilistic means to represent uncertainties in climate change projections. Here, we apply the storyline approach to 21st century projections of summer air stagnation over Europe and the United States. We use a Climate Model Intercomparison Project Phase 6 (CMIP6) ensemble to generate stagnation storylines based on the forced response of three remote drivers of the Northern Hemisphere mid-latitude atmospheric circulation: North Atlantic warming, North Pacific warming, and tropical versus Arctic warming. Under a high radiative forcing scenario (SSP5-8.5), models consistently project increases in stagnation over Europe and the U.S., but the magnitude and spatial distribution of changes vary substantially across CMIP6 ensemble members, suggesting that future projections are not well-constrained when using the ensemble mean alone. We find that the diversity of projected stagnation changes depends on the forced response of remote drivers in individual models. This is especially true in Europe, where differences of ∼2 summer stagnant days per degree of global warming are found amongst the different storyline combinations. For example, the greatest projected increase in stagnation for most European regions leads to the smallest increase in stagnation for southwestern Europe; i.e. limited North Atlantic warming combined with near-equitable tropical and Arctic warming. In the U.S., only the atmosphere over the northern Rocky Mountain states demonstrates comparable stagnation projection uncertainty, due to opposite influences of remote drivers on the meteorological conditions that lead to stagnation.

 

We present a simulation of the global present-day composition of the troposphere which includes the chemistry of halogens (Cl, Br, I). Building on previous work within the GEOS-Chem model we include emissions of inorganic iodine from the oceans, anthropogenic and biogenic sources of halogenated gases, gas phase chemistry, and a parameterised approach to heterogeneous halogen chemistry. Consistent with Schmidt et al. (2016) we do not include sea-salt debromination. Observations of halogen radicals (BrO, IO) are sparse but the model has some skill in reproducing these. Modelled IO shows both high and low biases when compared to different datasets, but BrO concentrations appear to be modelled low. Comparisons to the very sparse observations dataset of reactive Cl species suggest the model represents a lower limit of the impacts of these species, likely due to underestimates in emissions and therefore burdens. Inclusion of Cl, Br, and I results in a general improvement in simulation of ozone (O₃) concentrations, except in polar regions where the model now underestimates O₃ concentrations. Halogen chemistry reduces the global tropospheric O₃ burden by 18.6 %, with the O₃ lifetime reducing from 26 to 22 days. Global mean OH concentrations of 1.28  ×  10⁶ molecules cm⁻³ are 8.2 % lower than in a simulation without halogens, leading to an increase in the CH₄ lifetime (10.8 %) due to OH oxidation from 7.47 to 8.28 years. Oxidation of CH₄ by Cl is small (∼  2 %) but Cl oxidation of other VOCs (ethane, acetone, and propane) can be significant (∼  15–27 %). Oxidation of VOCs by Br is smaller, representing 3.9 % of the loss of acetaldehyde and 0.9 % of the loss of formaldehyde.