scholarly journals Emission location dependent ozone depletion potentials for very short-lived halogenated species

2010 ◽  
Vol 10 (6) ◽  
pp. 16277-16305
Author(s):  
I. Pisso ◽  
P. H. Haynes ◽  
K. S. Law
Keyword(s):  
Northern Hemisphere ◽  
Ozone Depletion ◽  
Degradation Products ◽  
Stratospheric Ozone ◽  
Surface Emission ◽  
Spatial And Seasonal Variation ◽  
Geographical Regions ◽  
Simplifying Assumptions ◽  
Hemisphere Winter ◽  
The Tropics

Abstract. We present trajectory-based estimates of Ozone Depletion Potentials (ODPs) for very short-lived halogenated source gases as a function of surface emission location. The ODPs are determined by the fraction of source gas and its degradation products which reach the stratosphere, depending primarily on tropospheric transport and chemistry, and the effect of the resulting reactive halogen in the stratosphere, which is determined by stratospheric transport and chemistry, in particular by stratospheric residence time. Reflecting the different timescales and physico-chemical processes in the troposphere and stratosphere, the estimates are based on calculation of separate ensembles of trajectories for the troposphere and stratosphere. A methodology is described by which information from the two ensembles can be combined to give the ODPs. The ODP estimates for a species with a 20 d lifetime, representing a compound like n-propyl bromide, are presented as an example. The estimated ODPs show strong geographical and season variation, particularly within the tropics. The values of the ODPs are sensitive to the inclusion of a convective parametrization in the trajectory calculations, but the relative spatial and seasonal variation is not. The results imply that ODPs are largest for emissions from South and South-East Asia during Northern Hemisphere summer and from the Western Pacific during Northern Hemisphere winter. Large ODPs are also estimated for emissions throughout the tropics with also non-negligible values extending into northern mid-latitudes particularly in the summer. These first estimates, which include some simplifying assumptions, show larger ODP values than previous studies, particularly over Southern Asia, suggesting that emissions of short-lived halogen source gases in certain geographical regions could have a significant impact on stratospheric ozone depletion.

scholarly journals Emission location dependent ozone depletion potentials for very short-lived halogenated species

2010 ◽  
Vol 10 (24) ◽  
pp. 12025-12036 ◽  
Author(s):  
I. Pisso ◽  
P. H. Haynes ◽  
K. S. Law
Keyword(s):  
Seasonal Variation ◽  
Northern Hemisphere ◽  
Ozone Depletion ◽  
Degradation Products ◽  
Surface Emission ◽  
Spatial And Seasonal Variation ◽  
Simplifying Assumptions ◽  
Land Surfaces ◽  
Hemisphere Winter ◽  
The Tropics

Abstract. We present trajectory-based estimates of Ozone Depletion Potentials (ODPs) for very short-lived halogenated source gases as a function of surface emission location. The ODPs are determined by the fraction of source gas and its degradation products which reach the stratosphere, depending primarily on tropospheric transport and chemistry, and the effect of the resulting reactive halogen in the stratosphere, which is determined by stratospheric transport and chemistry, in particular by stratospheric residence time. Reflecting the different timescales and physico-chemical processes in the troposphere and stratosphere, the estimates are based on calculation of separate ensembles of trajectories for the troposphere and stratosphere. A methodology is described by which information from the two ensembles can be combined to give the ODPs. The ODP estimates for a species with a fixed 20 d lifetime, representing a compound like n-propyl bromide, are presented as an example. The estimated ODPs show strong geographical and seasonal variation, particularly within the tropics. The values of the ODPs are sensitive to the inclusion of a convective parametrization in the trajectory calculations, but the relative spatial and seasonal variation is not. The results imply that ODPs are largest for emissions from south and south-east Asia during Northern Hemisphere summer and from the western Pacific during Northern Hemisphere winter. Large ODPs are also estimated for emissions throughout the tropics with non-negligible values also extending into northern mid-latitudes, particularly in the summer. These first estimates, whilst made under some simplifying assumptions, show larger ODPs for certain emission regions, particularly south Asia in NH summer, than have typically been reported by previous studies which used emissions distributed evenly over land surfaces.

scholarly journals The Toba supervolcano eruption caused severe tropical stratospheric ozone depletion

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Sergey Osipov ◽  
Georgiy Stenchikov ◽  
Kostas Tsigaridis ◽  
Allegra N. LeGrande ◽  
Susanne E. Bauer ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Water Cycle ◽  
Stratospheric Ozone ◽  
System Model ◽  
Earth System ◽  
Sulfate Aerosols ◽  
Winter Conditions ◽  
Attenuation Mechanism ◽  
The Tropics ◽  
Sulfur Emissions

AbstractSupervolcano eruptions have occurred throughout Earth’s history and have major environmental impacts. These impacts are mostly associated with the attenuation of visible sunlight by stratospheric sulfate aerosols, which causes cooling and deceleration of the water cycle. Supereruptions have been assumed to cause so-called volcanic winters that act as primary evolutionary factors through ecosystem disruption and famine, however, winter conditions alone may not be sufficient to cause such disruption. Here we use Earth system model simulations to show that stratospheric sulfur emissions from the Toba supereruption 74,000 years ago caused severe stratospheric ozone loss through a radiation attenuation mechanism that only moderately depends on the emission magnitude. The Toba plume strongly inhibited oxygen photolysis, suppressing ozone formation in the tropics, where exceptionally depleted ozone conditions persisted for over a year. This effect, when combined with volcanic winter in the extra-tropics, can account for the impacts of supereruptions on ecosystems and humanity.

scholarly journals Northern Hemisphere Stratospheric Ozone Depletion Caused by Solar Proton Events: The Role of the Polar Vortex

2018 ◽  
Vol 45 (4) ◽  
pp. 2115-2124 ◽  
Author(s):  
M. H. Denton ◽  
R. Kivi ◽  
T. Ulich ◽  
M. A. Clilverd ◽  
C. J. Rodger ◽  
...  
Keyword(s):  
Northern Hemisphere ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
Solar Proton ◽  
Stratospheric Ozone Depletion ◽  
Solar Proton Events

scholarly journals Copernicus stratospheric ozone service, 2009–2012: validation, system intercomparison and roles of input data sets

2015 ◽  
Vol 15 (5) ◽  
pp. 2269-2293 ◽  
Author(s):  
K. Lefever ◽  
R. van der A ◽  
F. Baier ◽  
Y. Christophe ◽  
Q. Errera ◽  
...  
Keyword(s):  
Data Assimilation ◽  
Atmospheric Chemistry ◽  
Ozone Depletion ◽  
Total Ozone ◽  
Chemical Constituents ◽  
Stratospheric Ozone ◽  
Atmospheric Composition ◽  
The Arctic ◽  
Data Sets ◽  
The Tropics

Abstract. This paper evaluates and discusses the quality of the stratospheric ozone analyses delivered in near real time by the MACC (Monitoring Atmospheric Composition and Climate) project during the 3-year period between September 2009 and September 2012. Ozone analyses produced by four different chemical data assimilation (CDA) systems are examined and compared: the Integrated Forecast System coupled to the Model for OZone And Related chemical Tracers (IFS-MOZART); the Belgian Assimilation System for Chemical ObsErvations (BASCOE); the Synoptic Analysis of Chemical Constituents by Advanced Data Assimilation (SACADA); and the Data Assimilation Model based on Transport Model version 3 (TM3DAM). The assimilated satellite ozone retrievals differed for each system; SACADA and TM3DAM assimilated only total ozone observations, BASCOE assimilated profiles for ozone and some related species, while IFS-MOZART assimilated both types of ozone observations. All analyses deliver total column values that agree well with ground-based observations (biases < 5%) and have a realistic seasonal cycle, except for BASCOE analyses, which underestimate total ozone in the tropics all year long by 7 to 10%, and SACADA analyses, which overestimate total ozone in polar night regions by up to 30%. The validation of the vertical distribution is based on independent observations from ozonesondes and the ACE-FTS (Atmospheric Chemistry Experiment – Fourier Transform Spectrometer) satellite instrument. It cannot be performed with TM3DAM, which is designed only to deliver analyses of total ozone columns. Vertically alternating positive and negative biases are found in the IFS-MOZART analyses as well as an overestimation of 30 to 60% in the polar lower stratosphere during polar ozone depletion events. SACADA underestimates lower stratospheric ozone by up to 50% during these events above the South Pole and overestimates it by approximately the same amount in the tropics. The three-dimensional (3-D) analyses delivered by BASCOE are found to have the best quality among the three systems resolving the vertical dimension, with biases not exceeding 10% all year long, at all stratospheric levels and in all latitude bands, except in the tropical lowermost stratosphere. The northern spring 2011 period is studied in more detail to evaluate the ability of the analyses to represent the exceptional ozone depletion event, which happened above the Arctic in March 2011. Offline sensitivity tests are performed during this month and indicate that the differences between the forward models or the assimilation algorithms are much less important than the characteristics of the assimilated data sets. They also show that IFS-MOZART is able to deliver realistic analyses of ozone both in the troposphere and in the stratosphere, but this requires the assimilation of observations from nadir-looking instruments as well as the assimilation of profiles, which are well resolved vertically and extend into the lowermost stratosphere.

scholarly journals Seasonal impact of biogenic very short-lived bromocarbons on lowermost stratospheric ozone between 60° N and 60° S during the 21st century

2020 ◽  
Vol 20 (13) ◽  
pp. 8083-8102
Author(s):  
Javier Alejandro Barrera ◽  
Rafael Pedro Fernandez ◽  
Fernando Iglesias-Suarez ◽  
Carlos Alberto Cuevas ◽  
Jean-Francois Lamarque ◽  
...  
Keyword(s):  
21St Century ◽  
Ozone Depletion ◽  
Hemispheric Asymmetry ◽  
Stratospheric Ozone ◽  
Ozone Loss ◽  
Seasonal Impact ◽  
Low Sensitivity ◽  
The Tropics ◽  
The Impact ◽  
Ozone Column

Abstract. Biogenic very short-lived bromocarbons (VSLBr) currently represent ∼25 % of the total stratospheric bromine loading. Owing to their much shorter lifetime compared to anthropogenic long-lived bromine (e.g. halons) and chlorine (e.g. chlorofluorocarbons), the impact of VSLBr on ozone peaks in the lowermost stratosphere, which is a key climatic and radiative atmospheric region. Here we present a modelling study of the evolution of stratospheric ozone and its chemical loss within the tropics and at mid-latitudes during the 21st century. Two different experiments are explored: considering and neglecting the additional stratospheric injection of 5 ppt biogenic bromine naturally released from the ocean. Our analysis shows that the inclusion of VSLBr results in a realistic stratospheric bromine loading and improves the agreement between the model and satellite observations of the total ozone column (TOC) for the 1980–2015 period at mid-latitudes. We show that the overall ozone response to VSLBr at mid-latitudes follows the stratospheric evolution of long-lived inorganic chlorine and bromine throughout the 21st century. Additional ozone loss due to VSLBr is maximized during the present-day period (1990–2010), with TOC differences of −8 DU (−3 %) and −5.5 DU (−2 %) for the Southern Hemisphere and Northern Hemisphere mid-latitudes (SH-MLs and NH-MLs), respectively. Moreover, the projected TOC differences at the end of the 21st century are ∼50 % lower than the values found for the present-day period. We find that seasonal VSLBr impact on lowermost stratospheric ozone at mid-latitude is influenced by the seasonality of the heterogeneous inorganic-chlorine reactivation processes on ice crystals. Indeed, due to the more efficient reactivation of chlorine reservoirs (mainly ClONO2 and HCl) within the colder SH-ML lowermost stratosphere, the seasonal VSLBr impact shows a small but persistent hemispheric asymmetry through the whole modelled period. Our results indicate that, although the overall VSLBr-driven ozone destruction is greatest during spring, the halogen-mediated (Halogx-Loss) ozone loss cycle in the mid-latitude lowermost stratosphere during winter is comparatively more efficient than the HOx cycle with respect to other seasons. Indeed, when VSLBr are considered, Halogx-Loss dominates wintertime lowermost stratospheric ozone loss at SH-MLs between 1985 and 2020, with a contribution of inter-halogen ClOx–BrOx cycles to Halogx-Loss of ∼50 %. Within the tropics, a small (<-2.5 DU) and relatively constant (∼-1 %) ozone depletion mediated by VSLBr is closely related to their fixed emissions throughout the modelled period. By including the VSLBr sources, the seasonal Halogx-Loss contribution to lowermost stratospheric ozone loss is practically dominated by the BrOx cycle, reflecting the low sensitivity of very short-lived (VSL) bromine to background halogen abundances to drive tropical stratospheric ozone depletion. We conclude that the link between biogenic bromine sources and seasonal changes in heterogeneous chlorine reactivation is a key feature for future projections of mid-latitude lowermost stratospheric ozone during the 21st century.

Impacts of Stratospheric Ozone Extremes on Arctic High Cloud

2021 ◽  
Author(s):  
Karen Smith ◽  
Sarah Maleska ◽  
John Virgin
Keyword(s):  
Northern Hemisphere ◽  
Ozone Depletion ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Global Climate Models ◽  
Arctic Climate ◽  
The Arctic ◽  
Stratospheric Ozone Depletion ◽  
High Cloud ◽  
The Impact

&lt;p&gt;Stratospheric ozone depletion in the Antarctic is well known to cause changes in Southern Hemisphere tropospheric climate; however, because of its smaller magnitude in the Arctic, the effects of stratospheric ozone depletion on Northern Hemisphere tropospheric climate are not as obvious or well understood. Recent research using both global climate models and observational data has determined that the impact of ozone depletion on ozone extremes can affect interannual variability in tropospheric circulation in the Northern Hemisphere in spring. To further this work, we use a coupled chemistry&amp;#8211;climate model to examine the difference in high cloud between years with anomalously low and high Arctic stratospheric ozone concentrations. We find that low ozone extremes during the late twentieth century, when ozone-depleting substances (ODS) emissions are higher, are related to a decrease in upper tropospheric stability and an increase in high cloud fraction, which may contribute to enhanced Arctic surface warming in spring through a positive longwave cloud radiative effect. A better understanding of how Arctic climate is affected by ODS emissions, ozone depletion, and ozone extremes will lead to improved predictions of Arctic climate and its associated feedbacks with atmospheric fields as ozone levels recover.&lt;/p&gt;

scholarly journals Two mechanisms of stratospheric ozone loss in the Northern hemisphere, studied using data assimilation of Odin/SMR atmospheric observations

2016 ◽  
Author(s):  
Kazutoshi Sagi ◽  
Kristell Pérot ◽  
Donal Murtagh ◽  
Yvan Orsolini
Keyword(s):  
Nitrogen Oxides ◽  
Data Assimilation ◽  
Northern Hemisphere ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Thermal Conditions ◽  
The Arctic ◽  
Ozone Loss ◽  
First Time ◽  
Middle Stratosphere

Abstract. Observations from the Odin/Sub-Millimetre Radiometer (SMR) instrument have been as- similated into the DIAMOND model (Dynamic Isentropic Assimilation Model for OdiN Data), in order to estimate the chemical ozone (O3) loss in the stratosphere. This data assimilation technique is described in Sagi and Murtagh (2016), in which it was used to study the inter-annual variability in ozone depletion during the entire Odin operational time and in both hemispheres. Our study focuses on the Arctic region, where two O3 destruction mechanisms play an important role, involving halogen and nitrogen oxides (NOx) chemical families, respectively. The temporal evolution and geographical distribution of O3 loss in the low and middle stratosphere have been investigated between 2002 and 2013. For the first time, this has been done based on the study of a series of winter-spring seasons over more than a decade, spanning very different dynamical conditions. The chemical mechanisms involved in O3 depletion are very sensitive to thermal conditions and dynamical activity, which are extremely variable in the Arctic stratosphere. We have focused our analysis on particularly cold and warm winters, in order to study the influence it has on ozone loss. The winter 2010/2011 is considered as an example for cold conditions. This case, that has been the subject of many studies, was characterised by a very stable vortex associated with particularly low temperatures, which led to an important halogen-induced O3 loss occurring inside the vortex in the lower stratosphere. We found a loss of 2.1 ppmv at an altitude of 450 K in the end of March 2011, which corresponds to the largest ozone depletion in the northern hemisphere observed during the last decade. This result is consistent with other studies. A similar situation was observed during the winters 2004/2005 and 2007/2008, although the amplitude of the O3 destruction was lower. To study the opposite situation, corresponding to a warm and unstable winter in the stratosphere, we performed a composite calculation of four selected cases, 2003/2004, 2005/2006, 2008/2009 and 2012/2013, which were all affected by a major mid-winter sudden stratospheric warming event, related to particularly high dynamical activity. We have shown that such conditions were associated with low O3 loss below 500 K, while O3 depletion in the middle stratosphere, where the role of NOx-induced destruction processes is prevailing, was particularly important. This can mainly be explained by the horizontal mixing of NOx-rich air from lower latitudes with vortex air, that takes place in case of strongly disturbed dynamical situation. In this manuscript, we show that the relative contribution of O3 depletion mechanisms occurring in the lower or in the middle stratosphere is dramatically influenced by dynamical and thermal conditions. We provide confirmation that the O3 loss driven by nitrogen oxides and triggered by stratospheric warmings can outweigh the effects of halogens in the case of a dynamically unstable Arctic winter. This is the first time that such a study has been performed over a long period of time, covering more than ten years of observations.

scholarly journals The initial dispersal and radiative forcing of a Northern Hemisphere mid-latitude super volcano: a model study

2006 ◽  
Vol 6 (1) ◽  
pp. 35-49 ◽  
Author(s):  
C. Timmreck ◽  
H.-F. Graf
Keyword(s):  
Northern Hemisphere ◽  
Radiative Forcing ◽  
Climate Model ◽  
Climate Anomalies ◽  
Model Study ◽  
Pinatubo Eruption ◽  
Volcanic Cloud ◽  
Hemisphere Winter ◽  
The Tropics ◽  
Fully Coupled

Abstract. The chemistry climate model MAECHAM4/ CHEM with interactive and prognostic volcanic aerosol and ozone was used to study the initial dispersal and radiative forcing of a possible Northern Hemisphere mid-latitude super eruption. Tropospheric climate anomalies are not analysed since sea surface temperatures are kept fixed. Our experiments show that the global dispersal of a super eruption located at Yellowstone, Wy. is strongly dependent on the season of the eruption. In Northern Hemisphere summer the volcanic cloud is transported westward and preferentially southward, while in Northern Hemisphere winter the cloud is transported eastward and more northward compared to the summer case. Aerosol induced heating leads to a more global spreading with a pronounced cross equatorial transport. For a summer eruption aerosol is transported much further to the Southern Hemisphere than for a winter eruption. In contrast to Pinatubo case studies, strong cooling tendencies appear with maximum peak values of less than −1.6 K/day three months after the eruption in the upper tropical stratosphere. This strong cooling effect weakens with decreasing aerosol density over time and initially prevents the aerosol laden air from further active rising. All-sky net radiative flux changes of less than −32 W/m2 at the surface are about a factor of 6 larger than for the Pinatubo eruption. Large positive flux anomalies of more than 16 W/m2 are found in the first months in the tropics and sub tropics. These strong forcings call for a fully coupled ocean/atmosphere/chemistry model to study climate sensitivity to such a super-eruption.

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