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 ◽  
...  

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.

2012 ◽  
Vol 12 (11) ◽  
pp. 5249-5257 ◽  
Author(s):  
S. Watanabe ◽  
T. Takemura ◽  
K. Sudo ◽  
T. Yokohata ◽  
H. Kawase

Abstract. The historical anthropogenic change in the surface all-sky UV-B (solar ultraviolet: 280–315 nm) radiation through 1850–2005 is evaluated using an Earth system model. Responses of UV-B dose to anthropogenic changes in ozone and aerosols are separately evaluated using a series of historical simulations including/excluding these changes. Increases in these air pollutants cause reductions in UV-B transmittance, which occur gradually/rapidly before/after 1950 in and downwind of industrial and deforestation regions. Furthermore, changes in ozone transport in the lower stratosphere, which is induced by increasing greenhouse gas concentrations, increase ozone concentration in the extratropical upper troposphere and lower stratosphere. These transient changes work to decrease the amount of UV-B reaching the Earth's surface, counteracting the well-known effect increasing UV-B due to stratospheric ozone depletion, which developed rapidly after ca. 1980. As a consequence, the surface UV-B radiation change between 1850 and 2000 is negative in the tropics and NH extratropics and positive in the SH extratropics. Comparing the contributions of ozone and aerosol changes to the UV-B change, the transient change in ozone absorption of UV-B mainly determines the total change in the surface UV-B radiation at most locations. On the other hand, the aerosol direct and indirect effects on UV-B play an equally important role to that of ozone in the NH mid-latitudes and tropics. A typical example is East Asia (25° N–60° N and 120° E–150° E), where the effect of aerosols (ca. 70%) dominates the total UV-B change.


2012 ◽  
Vol 12 (2) ◽  
pp. 4221-4242
Author(s):  
S. Watanabe ◽  
T. Takemura ◽  
K. Sudo ◽  
T. Yokohata ◽  
H. Kawase

Abstract. The historical anthropogenic change in the surface all-sky UV-B (solar ultraviolet: 280–315 nm) radiation through 1850–2005 is evaluated using an Earth system model. Responses of UV-B dose to anthropogenic changes in ozone and aerosols are separately evaluated using a series of historical simulations including/excluding these changes. Increases in these air pollutants cause reductions in UV-B transmittance, which occur gradually/rapidly before/after 1950 in and downwind of industrial and deforestation regions. Furthermore, changes in ozone transport in the lower stratosphere, which is induced by increasing greenhouse gas concentrations, increase ozone concentration in the extratropical upper troposphere and lower stratosphere. These transient changes work to decrease the amount of UV-B reaching the Earth's surface, counteracting the well-known effect increasing UV-B due to stratospheric ozone depletion, which developed rapidly after ca. 1980. As a consequence, the surface all-sky UV-B radiation change between 1850 and 2000 is negative in the tropics and NH extratropics and positive in the SH extratropics. Comparing the contributions of ozone and aerosol changes to the UV-B change, the transient change in ozone absorption of UV-B mainly determines the total change in the surface all-sky UV-B radiation at most locations. On the other hand, the aerosol direct and indirect effects on UV-B play an equally important role to that of ozone in the NH mid-latitudes and tropics. A typical example is East Asia (25° N–60° N and 120° E–150° E), where the effect of aerosols (ca. 70%) dominates the total UV-B change.


2021 ◽  
Vol 8 ◽  
Author(s):  
James Keeble ◽  
Yu Yeung Scott Yiu ◽  
Alexander T. Archibald ◽  
Fiona O’Connor ◽  
Alistair Sellar ◽  
...  

Stratospheric ozone projections in the tropics, modeled using the UKESM1 Earth system model, are explored under different Shared Socioeconomic Pathways (SSPs). Consistent with other studies, it is found that tropical stratospheric column ozone does not return to 1980s values by the end of the 21st century under any SSP scenario as increased ozone mixing ratios in the tropical upper stratosphere are offset by continued ozone decreases in the tropical lower stratosphere. Stratospheric column ozone is projected to be largest under SSP scenarios with the smallest change in radiative forcing, and smallest for SSP scenarios with larger radiative forcing, consistent with a faster Brewer-Dobson circulation at high greenhouse gas loadings. This study explores the use of machine learning (ML) techniques to make accurate, computationally inexpensive projections of tropical stratospheric column ozone. Four ML techniques are investigated: Ridge regression, Lasso regression, Random Forests and Extra Trees. All four techniques investigated here are able to make projections of future tropical stratospheric column ozone which agree well with those made by the UKESM1 Earth system model, often falling within the ensemble spread of UKESM1 simulations for a broad range of SSPs. However, all techniques struggle to make accurate projects for the final decades of the SSP5-8.5 scenario. Accurate projections can only be achieved when the ML methods are trained on sufficient data, including both historical and future simulations. When trained only on historical data, the projections made using models based on ML techniques fail to accurately predict tropical stratospheric ozone changes. Results presented here indicate that, when sufficiently trained, ML models have the potential to make accurate, computationally inexpensive projections of tropical stratospheric column ozone. Further development of these models may reduce the computational burden placed on fully coupled chemistry-climate and Earth system models and enable the exploration of tropical stratospheric column ozone recovery under a much broader range of future emissions scenarios.


2015 ◽  
Vol 12 (11) ◽  
pp. 3301-3320 ◽  
Author(s):  
K. B. Rodgers ◽  
J. Lin ◽  
T. L. Frölicher

Abstract. Marine ecosystems are increasingly stressed by human-induced changes. Marine ecosystem drivers that contribute to stressing ecosystems – including warming, acidification, deoxygenation and perturbations to biological productivity – can co-occur in space and time, but detecting their trends is complicated by the presence of noise associated with natural variability in the climate system. Here we use large initial-condition ensemble simulations with an Earth system model under a historical/RCP8.5 (representative concentration pathway 8.5) scenario over 1950–2100 to consider emergence characteristics for the four individual and combined drivers. Using a 1-standard-deviation (67% confidence) threshold of signal to noise to define emergence with a 30-year trend window, we show that ocean acidification emerges much earlier than other drivers, namely during the 20th century over most of the global ocean. For biological productivity, the anthropogenic signal does not emerge from the noise over most of the global ocean before the end of the 21st century. The early emergence pattern for sea surface temperature in low latitudes is reversed from that of subsurface oxygen inventories, where emergence occurs earlier in the Southern Ocean. For the combined multiple-driver field, 41% of the global ocean exhibits emergence for the 2005–2014 period, and 63% for the 2075–2084 period. The combined multiple-driver field reveals emergence patterns by the end of this century that are relatively high over much of the Southern Ocean, North Pacific, and Atlantic, but relatively low over the tropics and the South Pacific. For the case of two drivers, the tropics including habitats of coral reefs emerges earliest, with this driven by the joint effects of acidification and warming. It is precisely in the regions with pronounced emergence characteristics where marine ecosystems may be expected to be pushed outside of their comfort zone determined by the degree of natural background variability to which they are adapted. The results underscore the importance of sustained multi-decadal observing systems for monitoring multiple ecosystems drivers.


2015 ◽  
Vol 15 (13) ◽  
pp. 19161-19196
Author(s):  
K. A. Stone ◽  
O. Morgenstern ◽  
D. J. Karoly ◽  
A. R. Klekociuk ◽  
W. J. R. French ◽  
...  

Abstract. Chemistry climate models are important tools for addressing interactions of composition and climate in the Earth System. In particular, they are used for assessing the combined roles of greenhouse gases and ozone in Southern Hemisphere climate and weather. Here we present an evaluation of the Australian Community Climate and Earth System Simulator-Chemistry Climate Model, focusing on the Southern Hemisphere and the Australian region. This model is used for the Australian contribution to the international Chemistry-Climate Model Initiative, which is soliciting hindcast, future projection and sensitivity simulations. The model simulates global total column ozone (TCO) distributions accurately, with a slight delay in the onset and recovery of springtime Antarctic ozone depletion, and consistently higher ozone values. However, October averaged Antarctic TCO from 1960 to 2010 show a similar amount of depletion compared to observations. A significant innovation is the evaluation of simulated vertical profiles of ozone and temperature with ozonesonde data from Australia, New Zealand and Antarctica from 38 to 90° S. Excess ozone concentrations (up to 26.4 % at Davis during winter) and stratospheric cold biases (up to 10.1 K at the South Pole) outside the period of perturbed springtime ozone depletion are seen during all seasons compared to ozonesondes. A disparity in the vertical location of ozone depletion is seen: centered around 100 hPa in ozonesonde data compared to above 50 hPa in the model. Analysis of vertical chlorine monoxide profiles indicates that colder Antarctic stratospheric temperatures (possibly due to reduced mid-latitude heat flux) are artificially enhancing polar stratospheric cloud formation at high altitudes. The models inability to explicitly simulated supercooled ternary solution may also explain the lack of depletion at lower altitudes. The simulated Southern Annular Mode (SAM) index compares well with ERA-Interim data. Accompanying these modulations of the SAM, 50 hPa zonal wind differences between 2001–2010 and 1979–1998 show increasing zonal wind strength southward of 60° S during December for both the model simulations and ERA-Interim data. These model diagnostics shows that the model reasonably captures the stratospheric ozone driven chemistry-climate interactions important for Australian climate and weather while highlighting areas for future model development.


2010 ◽  
Vol 10 (6) ◽  
pp. 16277-16305
Author(s):  
I. Pisso ◽  
P. H. Haynes ◽  
K. S. Law

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.


2017 ◽  
Vol 10 (1) ◽  
pp. 271-319 ◽  
Author(s):  
Thomas Gasser ◽  
Philippe Ciais ◽  
Olivier Boucher ◽  
Yann Quilcaille ◽  
Maxime Tortora ◽  
...  

Abstract. This paper provides a comprehensive description of OSCAR v2.2, a simple Earth system model. The general philosophy of development is first explained, followed by a complete description of the model's drivers and various modules. All components of the Earth system necessary to simulate future climate change are represented in the model: the oceanic and terrestrial carbon cycles – including a book-keeping module to endogenously estimate land-use change emissions – so as to simulate the change in atmospheric carbon dioxide; the tropospheric chemistry and the natural wetlands, to simulate that of methane; the stratospheric chemistry, for nitrous oxide; 37 halogenated compounds; changing tropospheric and stratospheric ozone; the direct and indirect effects of aerosols; changes in surface albedo caused by black carbon deposition on snow and land-cover change; and the global and regional response of climate – in terms of temperature and precipitation – to all these climate forcers. Following the probabilistic framework of the model, an ensemble of simulations is made over the historical period (1750–2010). We show that the model performs well in reproducing observed past changes in the Earth system such as increased atmospheric concentration of greenhouse gases or increased global mean surface temperature.


2016 ◽  
Author(s):  
Thomas Gasser ◽  
Philippe Ciais ◽  
Olivier Boucher ◽  
Yann Quilcaille ◽  
Maxime Tortora ◽  
...  

Abstract. This paper provides a comprehensive description of OSCAR v2.2, a simple Earth system model. The general philosophy of development is first explained, it is then followed by a complete description of the model's drivers and various modules. All components of the Earth system necessary to simulate future climate change are represented in the model: the oceanic and terrestrial carbon-cycles – including a book-keeping module to endogenously estimate land-use change emissions – so as to simulate the change in atmospheric carbon dioxide; the tropospheric OH chemistry and the natural wetlands, to simulate that of methane; the stratospheric chemistry, for nitrous oxide; thirty-seven halogenated compounds; changing tropospheric and stratospheric ozone; the direct and indirect effects of aerosols; changes in surface albedo caused by black carbon deposition on snow and land-cover change; and the global and regional response of climate – in terms of temperatures and precipitations – to all these climate forcers. Following the probabilistic framework of the model, an ensemble of simulations is made over the historical period (1750–2010). We show that the model performs well in reproducing observed past changes in the Earth system such as increased atmospheric concentration of greenhouse gases or increased global mean surface temperature.


2015 ◽  
Vol 15 (5) ◽  
pp. 2269-2293 ◽  
Author(s):  
K. Lefever ◽  
R. van der A ◽  
F. Baier ◽  
Y. Christophe ◽  
Q. Errera ◽  
...  

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.


2020 ◽  
Author(s):  
Qi Tang ◽  
Michael J. Prather ◽  
Juno Hsu ◽  
Daniel J. Ruiz ◽  
Philip J. Cameron-Smith ◽  
...  

Abstract. Stratospheric ozone affects climate directly as the predominant heat source in the stratosphere and indirectly through chemical feedbacks controlling other greenhouse gases. The U.S. Department of Energy's Energy Exascale Earth System Model version 1 (E3SMv1) implemented a new ozone chemistry module that improves the simulation of the sharp tropopause gradients, replacing a version based partly on long-term average climatologies that poorly represented heating rates in the lowermost stratosphere. The new O3v2 module extends seamlessly into the troposphere and preserves the naturally sharp cross-tropopause gradient, with 20-40% less ozone in this region. Additionally, O3v2 enables the diagnosis of stratosphere-troposphere exchange flux of ozone, a key budget term lacking in E3SMv1. Here, we evaluate key features in ozone abundance and other closely related quantities in atmosphere-only E3SMv1 simulations driven by observed sea surface temperatures (SSTs, years 1990-2014), comparing with satellite observations and the University of California, Irvine chemistry transport model (UCI CTM) using the same stratospheric chemistry scheme but driven by European Centre forecast fields for the same period. In terms of stratospheric column ozone, O3v2 shows improved mean bias and northern mid-latitude variability, but not quite as good as the UCI CTM. As expected, SST forcing does not match the observed quasi-biennial oscillation, which is mostly matched with the UCI CTM. This new O3v2 E3SM model retains mostly the same climate state and climate sensitivity as the previous version, and we recommend its use for other climate models that still use ozone climatologies.


Sign in / Sign up

Export Citation Format

Share Document