scholarly journals Will climate change impact polar NOx produced by energetic particle precipitation?

Author(s):  
Ville Maliniemi ◽  
Daniel R. Marsh ◽  
Hilde Nesse Tyssøy ◽  
Christine Smith-Johnsen

<p>Energetic electron precipitation (EEP) is an important source of polar nitrogen oxides (NOx) in the upper atmosphere. During winter, mesospheric NOx has a long chemical lifetime and is transported to the stratosphere by the mean meridional circulation. Climate change is expected to accelerate this circulation and therefore increase polar mesospheric descent rates. We investigate the southern hemispheric polar NOx distribution during the 21<sup>st</sup> century under a variety of future scenarios using simulations of the Whole Atmosphere Community Climate Model (WACCM). Each future scenario has the same moderate variable solar activity scenario, where EEP activity is lower than during the 20<sup>th</sup> century. We simulate stronger polar mesospheric descent in all future scenarios that increase the atmospheric radiative forcing. By the end of 21<sup>st</sup> century polar NOx in the upper stratosphere is significantly enhanced in two future scenarios with the largest increase in radiative forcing. This indicates that the ozone depleting NOx cycle will become more important in the future, especially if stratospheric chlorine species decline. Thus, EEP-related atmospheric effects may become more prominent in the future.</p>

2021 ◽  
Author(s):  
Zhenze Liu ◽  
Ruth M. Doherty ◽  
Oliver Wild ◽  
Fiona M. O’Connor ◽  
Steven T. Turnock

<p>A new version of the UKCA chemistry-climate model with highly reactive volatile organic compounds (VOCs) is used to investigate the ozone (O<sub>3</sub>) responses in historical (2004-2014) and future (2045-2055) shared socio-economic pathways (SSPs) scenarios of CMIP6 AerChemMIP experiments. Significant increases in surface O<sub>3</sub> levels in South and East Asia are simulated in the new version compared with the standard UKCA model. The O<sub>3</sub> production and the O<sub>3</sub> burden averaged over the troposphere increase slightly by 6 % as a result of more highly reactive VOCs, but the O<sub>3</sub> lifetime is quite similar. Comparing the different SSP scenarios using this new model version we find the averaged surface O<sub>3</sub> concentrations are higher in the scenario with high emissions than for historical conditions. O<sub>3</sub> concentrations are much lower than historical O<sub>3</sub> concentrations when O<sub>3</sub> precursor concentrations are low. However, regional O<sub>3</sub> increases occur in East Asia in the future scenario with low emissions of short-lived climate forcers due to strong VOC limited regimes. Decreases in surface O<sub>3</sub> concentrations occur globally in the future scenario that has lower methane (CH<sub>4</sub>) concentrations. We construct O<sub>3</sub> and O<sub>3</sub> production isopleths. These both suggest that the threshold of NO<sub>x</sub>/VOCs shifting from NO<sub>x</sub> limited to VOC limited regimes is approximately 0.8. More areas become VOC limited in South Asia in all future scenarios, but there is little change for East Asia. The hydroxyl radical (OH) concentrations generally increase in regions with high O<sub>3</sub> precursor abundances in the future scenario, but the high OH levels are offset by lower CH<sub>4</sub> concentrations in the future low CH<sub>4</sub> scenario. We find that there are small changes in O<sub>3</sub> production efficiency in continental regions in all future scenarios. Relative O<sub>3</sub> burden changes between the future SSP and historical scenarios are larger in the troposphere than in the planetary boundary layer (PBL), illustrating that O<sub>3</sub> burdens are less sensitive in the PBL under emission and climate change. The O<sub>3</sub> lifetime in the troposphere decreases in all future scenarios as compared to the historical period. We find that the decreases in O<sub>3</sub> precursors and CH<sub>4</sub> concentrations play important roles in reducing O<sub>3</sub> burdens in the future.</p>


2021 ◽  
Author(s):  
Ville Maliniemi ◽  
Pavle Arsenovic ◽  
Hilde Nesse Tyssøy ◽  
Christine Smith-Johnsen ◽  
Daniel R. Marsh

<p>Ozone is expected to fully recover from the CFC-era by the end of the 21st century. Furthermore, because of the anthropogenic climate change, cooler stratosphere accelerates the ozone production and is projected to lead to a super recovery. We investigate the ozone distribution over the 21st century with four different future scenarios using simulations of the Whole Atmosphere Community Climate Model (WACCM). At the end of the 21st century, higher polar ozone levels than pre CFC-era are obtained in scenarios that have highest atmospheric radiative forcing. This is true in the Arctic stratosphere and the Antarctic lower stratosphere. The Antarctic upper stratosphere forms an exception, where different scenarios have similar level of ozone during winter. This results from excess nitrogen oxides (NOx) descending from above in stronger future scenarios. NOx is formed by energetic electron precipitation (EEP) in the thermosphere and the upper mesosphere, and descends faster through the mesosphere in stronger scenarios. This indicates that the EEP indirect effect will be important factor for the future Antarctic ozone evolution, and is potentially able to prevent the super recovery in the upper stratosphere.</p>


2021 ◽  
Vol 21 (10) ◽  
pp. 7639-7669
Author(s):  
Thomas Drugé ◽  
Pierre Nabat ◽  
Marc Mallet ◽  
Samuel Somot

Abstract. This study investigates, through regional climate modelling, the surface mass concentration and AOD (aerosol optical depth) evolution of the various (anthropogenic and natural) aerosols over the Euro-Mediterranean region between the end of the 20th century and the mid-21st century. The direct aerosol radiative forcing (DRF) as well as the future Euro-Mediterranean climate sensitivity to aerosols have also been analysed. Different regional climate simulations were carried out with the CNRM-ALADIN63 regional climate model, driven by the global CNRM-ESM2-1 Earth system model (used in CMIP6) and coupled to the TACTIC (Tropospheric Aerosols for ClimaTe In CNRM) interactive aerosol scheme. These simulations follow several future scenarios called shared socioeconomic pathways (SSP 1-1.9, SSP 3-7.0 and SSP 5-8.5), which have been chosen to analyse a wide range of possible future scenarios in terms of aerosol or particle precursor emissions. Between the historical and the future period, results show a total AOD decrease between 30 % and 40 % over Europe for the three scenarios, mainly due to the sulfate AOD decrease (between −85 and −93 %), that is partly offset by the nitrate and ammonium particles AOD increase (between +90 and +120 %). According to these three scenarios, nitrate aerosols become the largest contributor to the total AOD during the future period over Europe, with a contribution between 43.5 % and 47.5 %. It is important to note that one of the precursors of nitrate and ammonium aerosols, nitric acid, has been implemented in the model as a constant climatology over time. Concerning natural aerosols, their contribution to the total AOD increases slightly between the two periods. The different evolution of aerosols therefore impacts their DRF, with a significant sulfate DRF decrease between 2.4 and 2.8 W m−2 and a moderate nitrate and ammonium DRF increase between 1.3 and 1.5 W m−2, depending on the three scenarios over Europe. These changes, which are similar under the different scenarios, explain about 65 % of the annual shortwave radiation change but also about 6 % (in annual average) of the warming expected over Europe by the middle of the century. This study shows, with SSP 5-8.5, that the extra warming attributable to the anthropogenic aerosol evolution over Central Europe and the Iberian Peninsula during the summer period is due to “aerosol–radiation” as well as “aerosol–cloud” interaction processes. The extra warming of about 0.2 ∘C over Central Europe is explained by a surface radiation increase of 5.8 W m−2 over this region, due to both a surface aerosol DRF decrease of 4.4 W m−2 associated with a positive effective radiative forcing due to aerosol–radiation interactions (ERFari) of 2.7 W m−2 at the top of the atmosphere (TOA) and a cloud optical depth (COD) decrease of 1.3. In parallel, the simulated extra warming of 0.2∘C observed over the Iberian Peninsula is due to a COD decrease of 1.3, leading to a positive effective radiative forcing due to aerosol–cloud interactions (ERFaci) of 2.6 W m−2 at the TOA but also to an atmospheric dynamics change leading to a cloud cover decrease of about 1.7 % and drier air in the lower layers, which is a signature of the semi-direct forcing. This study thus highlights the necessity of taking into account the evolution of aerosols in future regional climate simulations.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Zhili Wang ◽  
Lei Lin ◽  
Yangyang Xu ◽  
Huizheng Che ◽  
Xiaoye Zhang ◽  
...  

AbstractAnthropogenic aerosol (AA) forcing has been shown as a critical driver of climate change over Asia since the mid-20th century. Here we show that almost all Coupled Model Intercomparison Project Phase 6 (CMIP6) models fail to capture the observed dipole pattern of aerosol optical depth (AOD) trends over Asia during 2006–2014, last decade of CMIP6 historical simulation, due to an opposite trend over eastern China compared with observations. The incorrect AOD trend over China is attributed to problematic AA emissions adopted by CMIP6. There are obvious differences in simulated regional aerosol radiative forcing and temperature responses over Asia when using two different emissions inventories (one adopted by CMIP6; the other from Peking university, a more trustworthy inventory) to driving a global aerosol-climate model separately. We further show that some widely adopted CMIP6 pathways (after 2015) also significantly underestimate the more recent decline in AA emissions over China. These flaws may bring about errors to the CMIP6-based regional climate attribution over Asia for the last two decades and projection for the next few decades, previously anticipated to inform a wide range of impact analysis.


2020 ◽  
Vol 13 (2) ◽  
Author(s):  
Salah Ouhamdouch ◽  
Mohammed Bahir ◽  
Driss Ouazar ◽  
Abdelmalek Goumih ◽  
Kamel Zouari

2006 ◽  
Vol 54 (6-7) ◽  
pp. 9-15 ◽  
Author(s):  
M. Grum ◽  
A.T. Jørgensen ◽  
R.M. Johansen ◽  
J.J. Linde

That we are in a period of extraordinary rates of climate change is today evident. These climate changes are likely to impact local weather conditions with direct impacts on precipitation patterns and urban drainage. In recent years several studies have focused on revealing the nature, extent and consequences of climate change on urban drainage and urban runoff pollution issues. This study uses predictions from a regional climate model to look at the effects of climate change on extreme precipitation events. Results are presented in terms of point rainfall extremes. The analysis involves three steps: Firstly, hourly rainfall intensities from 16 point rain gauges are averaged to create a rain gauge equivalent intensity for a 25 × 25 km square corresponding to one grid cell in the climate model. Secondly, the differences between present and future in the climate model is used to project the hourly extreme statistics of the rain gauge surface into the future. Thirdly, the future extremes of the square surface area are downscaled to give point rainfall extremes of the future. The results and conclusions rely heavily on the regional model's suitability in describing extremes at time-scales relevant to urban drainage. However, in spite of these uncertainties, and others raised in the discussion, the tendency is clear: extreme precipitation events effecting urban drainage and causing flooding will become more frequent as a result of climate change.


2016 ◽  
Author(s):  
Malte Meinshausen ◽  
Elisabeth Vogel ◽  
Alexander Nauels ◽  
Katja Lorbacher ◽  
Nicolai Meinshausen ◽  
...  

Abstract. Atmospheric greenhouse gas concentrations are at unprecedented, record-high levels compared to pre-industrial reconstructions over the last 800,000 years. Those elevated greenhouse gas concentrations warm the planet and together with net cooling effects by aerosols, they are the reason of observed climate change over the past 150 years. An accurate representation of those concentrations is hence important to understand and model recent and future climate change. So far, community efforts to create composite datasets with seasonal and latitudinal information have focused on marine boundary layer conditions and recent trends since 1980s. Here, we provide consolidated data sets of historical atmospheric (volume) mixing ratios of 43 greenhouse gases specifically for the purpose of climate model runs. The presented datasets are based on AGAGE and NOAA networks and a large set of literature studies. In contrast to previous intercomparisons, the new datasets are latitudinally resolved, and include seasonality over the period between year 0 to 2014. We assimilate data for CO2, methane (CH4) and nitrous oxide (N2O), 5 chlorofluorocarbons (CFCs), 3 hydrochlorofluorocarbons (HCFCs), 16 hydrofluorocarbons (HFCs), 3 halons, methyl bromide (CH3Br), 3 perfluorocarbons (PFCs), sulfur hexafluoride (SF6), nitrogen triflouride (NF3) and sulfuryl fluoride (SO2F2). We estimate 1850 annual and global mean surface mixing ratios of CO2 at 284.3 ppmv, CH4 at 808.2 ppbv and N2O at 273.0 ppbv and quantify the seasonal and hemispheric gradients of surface mixing ratios. Compared to earlier intercomparisons, the stronger implied radiative forcing in the northern hemisphere winter (due to the latitudinal gradient and seasonality) may help to improve the skill of climate models to reproduce past climate and thereby reduce uncertainty in future projections.


2009 ◽  
Vol 22 (8) ◽  
pp. 1944-1961 ◽  
Author(s):  
Bariş Önol ◽  
Fredrick H. M. Semazzi

Abstract In this study, the potential role of global warming in modulating the future climate over the eastern Mediterranean (EM) region has been investigated. The primary vehicle of this investigation is the Abdus Salam International Centre for Theoretical Physics Regional Climate Model version 3 (ICTP-RegCM3), which was used to downscale the present and future climate scenario simulations generated by the NASA’s finite-volume GCM (fvGCM). The present-day (1961–90; RF) simulations and the future climate change projections (2071–2100; A2) are based on the Intergovernmental Panel on Climate Change (IPCC) greenhouse gas (GHG) emissions. During the Northern Hemispheric winter season, the general increase in precipitation over the northern sector of the EM region is present both in the fvGCM and RegCM3 model simulations. The regional model simulations reveal a significant increase (10%–50%) in winter precipitation over the Carpathian Mountains and along the east coast of the Black Sea, over the Kackar Mountains, and over the Caucasus Mountains. The large decrease in precipitation over the southeastern Turkey region that recharges the Euphrates and Tigris River basins could become a major source of concern for the countries downstream of this region. The model results also indicate that the autumn rains, which are primarily confined over Turkey for the current climate, will expand into Syria and Iraq in the future, which is consistent with the corresponding changes in the circulation pattern. The climate change over EM tends to manifest itself in terms of the modulation of North Atlantic Oscillation. During summer, temperature increase is as large as 7°C over the Balkan countries while changes for the rest of the region are in the range of 3°–4°C. Overall the temperature increase in summer is much greater than the corresponding changes during winter. Presentation of the climate change projections in terms of individual country averages is highly advantageous for the practical interpretation of the results. The consistence of the country averages for the RF RegCM3 projections with the corresponding averaged station data is compelling evidence of the added value of regional climate model downscaling.


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