Stratospheric Aerosol Injection (SAI) is a proposed method of climate intervention aiming to reduce the impacts of human-induced global warming by reflecting a portion of incoming solar radiation. Many studies have demonstrated that SAI would successfully reduce global-mean surface air temperatures, however the vast array of potential scenarios and strategies for deployment result in a diverse range of climate impacts. Here we compare two SAI strategies - a quasi- equatorial injection and a multi-latitude off-equatorial injection - simulated with the UK Earth System Model (UKESM1), both aiming to reduce the global-mean surface temperature from that of a high-end emissions scenario to that of a moderate emissions scenario. Both strategies effectively reduce global mean surface air temperatures by around 3°C by the end of the century; however, there are significant differences in the resulting regional temperature and precipitation patterns. We compare changes in the surface and stratospheric climate under each strategy to determine how the climate response depends on the injection location. In agreement with previous studies, an equatorial injection results in a tropospheric overcooling in the tropics and a residual warming in the polar regions, with substantial changes to stratospheric temperatures, water vapour and circulation. However, we demonstrate that by utilising a feedback controller in an off-equatorial injection strategy, regional surface temperature and precipitation changes relative to the target can be minimised. We conclude that moving the injection away from the equator minimises unfavourable changes to the climate, calling for a new series of inter-model SAI comparisons using an off-equatorial strategy.

Major tropical volcanic eruptions have emitted large quantities of stratospheric sulphate and are potential sources of stratospheric chlorine although this is less well constrained by observations. This study combines model and ice core analysis to investigate past changes in total column ozone. Historic eruptions are a good analogue for future eruptions as stratospheric chlorine levels have been decreasing since the year 2000. We perturb the pre-industrial atmosphere of a chemistry-climate model with high and low emissions of sulphate and chlorine. The sign of the resulting Antarctic ozone change is highly sensitive to the background stratospheric chlorine loading. In the first year, the response is dynamical, with ozone increases over Antarctica. In the high HCl (10 Tg emission) experiment, the injected chlorine is slowly transported to the polar regions with subsequent chemical ozone depletion. These model results are then compared to measurements of the stable nitrogen isotopic ratio, δ15N(NO−3), from a low snow accumulation Antarctic ice core from Dronning Maud Land (recovered in 2016-17). We expect ozone depletion to lead to increased surface ultraviolet (UV) radiation, enhanced air-snow nitrate photo-chemistry and enrichment in δ15N(NO−3) in the ice core. We focus on the possible ozone depletion event that followed the largest volcanic eruption in the past 1000 years, Samalas in 1257. The characteristic sulphate signal from this volcano is present in the ice-core but the variability in the δ15N(NO−3) dominates any signal arising from changes in UV from ozone depletion. Whether Samalas caused ozone depletion over Antarctica remains an open question.

The widespread presence of meteoric smoke particles (MSPs) within a distinct class of stratospheric aerosol particles has become clear from in-situ measurements in the Arctic, Antarctic and at mid-latitudes. We apply an adapted version of the interactive stratosphere aerosol configuration of the composition-climate model UM-UKCA, to predict the global distribution of meteoric-sulphuric particles nucleated heterogeneously on MSP cores. We compare the UM-UKCA results to new MSP-sulphuric simulations with the European stratosphere-troposphere chemistry-aerosol modelling system IFS-CB05-BASCOE-GLOMAP. The simulations show a strong seasonal cycle in meteoric-sulphuric particle abundance results from the winter-time source of MSPs transported down into the stratosphere in the polar vortex. Coagulation during downward transport sees high latitude MSP concentrations reduce from ~500 per cm3 at 40km to ~20 per cm3 at 25km, the uppermost extent of the stratospheric aerosol particle layer (the Junge layer). Once within the Junge layer’s supersaturated environment, meteoric-sulphuric particles form readily on the MSP cores, growing to 50-70nm dry-diameter (Dp) at 20-25km. Further inter-particle coagulation between these non-volatile particles reduces their number to 1-5 per cc at 15-20km, particle sizes there larger, at Dp ~100nm. The model predicts meteoric-sulphurics in high-latitude winter comprise >90% of Dp > 10nm particles above 25km, reducing to ~40% at 20km, and ~10% at 15km. These non-volatile particle fractions are slightly less than measured from high-altitude aircraft in the lowermost Arctic stratosphere (Curtius et al., 2005; Weigel et al., 2014), and consistent with mid-latitude aircraft measurements of lower stratospheric aerosol composition (Murphy et al., 1998), total particle concentrations also matching in-situ balloon measurements from Wyoming (Campbell and Deshler, 2014). The MSP-sulphuric interactions also improve agreement with SAGE-II observed stratospheric aerosol extinction in the quiescent 1998-2002 period. Simulations with a factor-8-elevated MSP input form more Dp>10nm meteoric-sulphurics, but the increased number sees fewer growing to Dp ~100nm, the increased MSPs reducing the stratospheric aerosol layer’s light extinction.