Energetic electron precipitation and their atmospheric effect

Energetic particle precipitation induces ionization of the atmosphere which initiates a chain of reaction cycles affecting atmospheric composition and dynamics potentially down to surface weather systems. Ionization rates are retrieved based on yield functions or pre-calculated monoenergetic electron flux and energy spectra of precipitated energetic particles. Usually, information about energy spectra is obtained from satellites, balloons, and various ground-based observations. In all cases, some assumptions about spectral distribution for the entire energy range have to be made. As ionization rates are widely used in chemistry-climate models to estimate the atmospheric response to particle forcing, evaluation of the energy spectra is a key task in the solar-terrestrial studies. In this paper, it is shown that possible uncertainties of the ionization rates retrieval based on different spectral functions can lead to large disagreements in the ionization rates, with implications for the modelled response of atmospheric composition and dynamics to electron precipitation

Attribution of chemistry-climate model initiative (CCMI) ozone radiative flux bias from satellites

The top-of-atmosphere (TOA) outgoing longwave flux over the 9.6 µm ozone band is a fundamental quantity for understanding chemistry–climate coupling. However, observed TOA fluxes are hard to estimate as they exhibit considerable variability in space and time that depend on the distributions of clouds, ozone (O3), water vapor (H2O), air temperature (Ta), and surface temperature (Ts). Benchmarking present-day fluxes and quantifying the relative influence of their drivers is the first step for estimating climate feedbacks from ozone radiative forcing and predicting radiative forcing evolution. To that end, we constructed observational instantaneous radiative kernels (IRKs) under clear-sky conditions, representing the sensitivities of the TOA flux in the 9.6 µm ozone band to the vertical distribution of geophysical variables, including O3, H2O, Ta, and Ts based upon the Aura Tropospheric Emission Spectrometer (TES) measurements. Applying these kernels to present-day simulations from the Chemistry-Climate Model Initiative (CCMI) project as compared to a 2006 reanalysis assimilating satellite observations, we show that the models have large differences in TOA flux, attributable to different geophysical variables. In particular, model simulations continue to diverge from observations in the tropics, as reported in previous studies of the Atmospheric Chemistry Climate Model Intercomparison Project (ACCMIP) simulations. The principal culprits are tropical middle and upper tropospheric ozone followed by tropical lower tropospheric H2O. Five models out of the eight studied here have TOA flux biases exceeding 100 mW m−2 attributable to tropospheric ozone bias. Another set of five models have flux biases over 50 mW m−2 due to H2O. On the other hand, Ta radiative bias is negligible in all models (no more than 30 mW m−2). We found that the atmospheric component (AM3) of the Geophysical Fluid Dynamics Laboratory (GFDL) general circulation model and Canadian Middle Atmosphere Model (CMAM) have the lowest TOA flux biases globally but are a result of cancellation of opposite biases due to different processes. Overall, the multi-model ensemble mean bias is −133±98  mW m−2, indicating that they are too atmospherically opaque due to trapping too much radiation in the atmosphere by overestimated tropical tropospheric O3 and H2O. Having too much O3 and H2O in the troposphere would have different impacts on the sensitivity of TOA flux to O3 and these competing effects add more uncertainties on the ozone radiative forcing. We find that the inter-model TOA outgoing longwave radiation (OLR) difference is well anti-correlated with their ozone band flux bias. This suggests that there is significant radiative compensation in the calculation of model outgoing longwave radiation

Modeling of the atmospheric response to a strong decrease of the solar activity

We estimate the consequences of a potential strong decrease of the solar activity using the model simulations of the future driven by pure anthropogenic forcing as well as its combination with different solar activity related factors: total solar irradiance, spectral solar irradiance, energetic electron precipitation, solar protons and galactic cosmic rays. The comparison of the model simulations shows that introduced strong decrease of solar activity can lead to some delay of the ozone recovery and partially compensate greenhouse warming acting in the direction opposite to anthropogenic effects. The model results also show that all considered solar forcings are important in different atmospheric layers and geographical regions. However, in the global scale the solar irradiance variability can be considered as the most important solar forcing. The obtained results constitute probably the upper limit of the possible solar influence. Development of the better constrained set of future solar forcings is necessary to address the problem of future climate and ozone layer with more confidenc

Montreal Protocol's impact on the ozone layer and climate

It is now recognized and confirmed that the ozone layer shields the biosphere from dangerous solar UV radiation and is also important for the global atmosphere and climate. The observed massive ozone depletion forced the introduction of limitations on the production of halogen-containing ozone-depleting substances (hODS) by the Montreal Protocol and its Amendments (MPA). Further research was aimed at analyzing the role played by the Montreal Protocol to increase public awareness of its necessity. In this study, we evaluate the benefits of the Montreal Protocol on climate and ozone evolution using the Earth system model (ESM) SOCOLv4.0 which includes dynamic ocean, sea ice, interactive ozone, and stratospheric aerosol modules. Here, we analyze the results of the numerical experiments performed with and without limitations on the ozone-depleting substances emissions. In the experiments, we have used CMIP6 SSP2-4.5 and SSP5-8.5 scenarios for future forcing behavior. We confirm previous results relative to catastrophic ozone layer depletion in the case without MPA limitations. The climate effects of MPA consist of additional global mean warming by up to 2.5 K in 2100 caused by the direct radiative effect of the hODS. We also obtained dramatic changes in several essential climate variables such as regional surface air temperature, sea-ice cover, and precipitation fields. Our research updates and complements previous modeling studies on the quantification of MPA benefits for the terrestrial atmosphere and climate.</p

Exceptional middle latitude electron precipitation detected by balloon observations: implications for atmospheric composition

Energetic particle precipitation leads to ionization in the Earth\u27s atmosphere, initiating the formation of active chemical species which destroy ozone and have the potential to impact atmospheric composition and dynamics down to the troposphere. We report on one exceptionally strong high-energy electron precipitation event detected by balloon measurements in middle latitudes on 14 December 2009 with ionization rates locally comparable to strong solar proton events. This electron precipitation was likely caused by wave-particle interactions in the slot region between the inner and outer radiation belts, connected with still not well understood natural phenomena in the magnetosphere. Satellite observations of odd nitrogen and nitric acid are consistent with wide-spread electron precipitation into magnetic midlatitudes. Simulations with a 3D chemistry-climate model indicate almost complete destruction of ozone in the upper mesosphere over the region where high-energy electron precipitation occurred. Such an extraordinary type of energetic particle precipitation can have major implications for the atmosphere, and their frequency and strength should be carefully studied

Exceptional middle latitude electron precipitation detected by balloon observations: implications for atmospheric composition

Energetic particle precipitation leads to ionization in the Earth\u27s atmosphere, initiating the formation of active chemical species which destroy ozone and have the potential to impact atmospheric composition and dynamics down to the troposphere. We report on one exceptionally strong high-energy electron precipitation event detected by balloon measurements in geomagnetic midlatitudes on 14 December 2009, with ionization rates locally comparable to strong solar proton events. This electron precipitation was possibly caused by wave–particle interactions in the slot region between the inner and outer radiation belts, connected with still poorly understood natural phenomena in the magnetosphere. Satellite observations of odd nitrogen and nitric acid are consistent with widespread electron precipitation into magnetic midlatitudes. Simulations with a 3D chemistry–climate model indicate the almost complete destruction of ozone in the upper mesosphere over the region where high-energy electron precipitation occurred. Such an extraordinary type of energetic particle precipitation can have major implications for the atmosphere, and their frequency and strength should be carefully studied

The Impact of Stratospheric Ozone Recovery on Tropopause Height Trends

The evolution of the tropopause in the past, present, and future climate is examined by analyzing a set of long-term integrations with stratosphere-resolving chemistry climate models (CCMs). These CCMs have high vertical resolution near the tropopause, a model top located in the mesosphere or above, and, most important, fully interactive stratospheric chemistry. Using such CCM integrations, it is found that the tropopause pressure (height) will continue to decrease (increase) in the future, but with a trend weaker than that in the recent past. The reduction in the future tropopause trend is shown to be directly associated with stratospheric ozone recovery. A significant ozone recovery occurs in the Southern Hemisphere lower stratosphere of the CCMs, and this leads to a relative warming there that reduces the tropopause trend in the twenty-first century. The future tropopause trends predicted by the CCMs are considerably smaller than those predicted by the Intergovernmental Panel on Climate Change Fourth Assessment Report (AR4) models, especially in the southern high latitudes. This difference persists even when the CCMs are compared with the subset of the AR4 model integrations for which stratospheric ozone recovery was prescribed. These results suggest that a realistic representation of the stratospheric processes might be important for a reliable estimate of tropopause trends. The implications of these finding for the Southern Hemisphere climate change are also discussed

The role of methane in projections of 21st century stratospheric water vapour

Stratospheric water vapour (SWV) is an important component of the Earth’s atmosphere as it affects both radiative balance and the chemistry of the atmosphere. Key processes driving changes in SWV include dehydration of air masses transiting the cold-point tropopause (CPT) and methane oxidation. We use a chemistry–climate model to simulate changes in SWV through the 21st century following the four canonical representative concentration pathways (RCPs). Furthermore, we quantify the contribution that methane oxidation makes to SWV following each of the RCPs. Although the methane contribution to SWV maximizes in the upper stratosphere, modelled SWV trends are found to be driven predominantly by warming of the CPT rather than by increasing methane oxidation. SWV changes by -5 to 60% (depending on the location in the atmosphere and emissions scenario) and increases in the lower stratosphere in all RCPs through the 21st century. Because the lower stratosphere is where water vapour radiative forcing maximizes, SWV’s influence on surface climate is also expected to increase through the 21st century