scholarly journals Impact of biogenic very short-lived bromine on the Antarctic ozone hole during the 21<sup>st</sup> century

Author(s):  
Rafael P. Fernandez ◽  
Douglas E. Kinnison ◽  
Jean-Francois Lamarque ◽  
Simone Tilmes ◽  
Alfonso Saiz-Lopez

Abstract. Active bromine released from the photochemical decomposition of biogenic very short-lived bromocarbons (VSLBr) enhances stratospheric ozone depletion. Based on a dual set of 1960–2100 coupled chemistry-climate simulations (i.e. with and without VSLBr), we show that the maximum Antarctic ozone hole depletion increases by up to 14 % when natural VSLBr are considered, in better agreement with ozone observations. The impact of the additional 5 pptv VSLBr on Antarctic ozone is most evident in the periphery of the ozone hole, producing an expansion of the ozone hole area of ~5 million km2, which is equivalent in magnitude to the recently estimated Antarctic ozone healing due to the implementation of the Montreal Protocol. We find that the inclusion of VSLBr in CAM-Chem does not introduce a significant delay of the modelled ozone return date to 1980 October levels, but instead affect the depth and duration of the simulated ozone hole. Our analysis further shows that total bromine-catalysed ozone destruction in the lower stratosphere surpasses that of chlorine by year 2070, and indicates that natural VSLBr chemistry would dominate Antarctic ozone seasonality before the end of the 21st century. This work suggests a large influence of biogenic bromine on the future Antarctic ozone layer.

2017 ◽  
Vol 17 (3) ◽  
pp. 1673-1688 ◽  
Author(s):  
Rafael P. Fernandez ◽  
Douglas E. Kinnison ◽  
Jean-Francois Lamarque ◽  
Simone Tilmes ◽  
Alfonso Saiz-Lopez

Abstract. Active bromine released from the photochemical decomposition of biogenic very short-lived bromocarbons (VSLBr) enhances stratospheric ozone depletion. Based on a dual set of 1960–2100 coupled chemistry–climate simulations (i.e. with and without VSLBr), we show that the maximum Antarctic ozone hole depletion increases by up to 14 % when natural VSLBr are considered, which is in better agreement with ozone observations. The impact of the additional 5 pptv VSLBr on Antarctic ozone is most evident in the periphery of the ozone hole, producing an expansion of the ozone hole area of ∼ 5 million km2, which is equivalent in magnitude to the recently estimated Antarctic ozone healing due to the implementation of the Montreal Protocol. We find that the inclusion of VSLBr in CAM-Chem (Community Atmosphere Model with Chemistry, version 4.0) does not introduce a significant delay of the modelled ozone return date to 1980 October levels, but instead affects the depth and duration of the simulated ozone hole. Our analysis further shows that total bromine-catalysed ozone destruction in the lower stratosphere surpasses that of chlorine by the year 2070 and indicates that natural VSLBr chemistry would dominate Antarctic ozone seasonality before the end of the 21st century. This work suggests a large influence of biogenic bromine on the future Antarctic ozone layer.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
S. S. Dhomse ◽  
W. Feng ◽  
S. A. Montzka ◽  
R. Hossaini ◽  
J. Keeble ◽  
...  

AbstractThe Antarctic ozone hole is decreasing in size but this recovery will be affected by atmospheric variability and any unexpected changes in chlorinated source gas emissions. Here, using model simulations, we show that the ozone hole will largely cease to occur by 2065 given compliance with the Montreal Protocol. If the unusual meteorology of 2002 is repeated, an ozone-hole-free-year could occur as soon as the early 2020s by some metrics. The recently discovered increase in CFC-11 emissions of ~ 13 Gg yr−1 may delay recovery. So far the impact on ozone is small, but if these emissions indicate production for foam use much more CFC-11 may be leaked in the future. Assuming such production over 10 years, disappearance of the ozone hole will be delayed by a few years, although there are significant uncertainties. Continued, substantial future CFC-11 emissions of 67 Gg yr−1 would delay Antarctic ozone recovery by well over a decade.


2014 ◽  
Vol 14 (19) ◽  
pp. 10431-10438 ◽  
Author(s):  
X. Yang ◽  
N. L. Abraham ◽  
A. T. Archibald ◽  
P. Braesicke ◽  
J. Keeble ◽  
...  

Abstract. Naturally produced very short-lived substances (VSLS) account for almost a quarter of the current stratospheric inorganic bromine, Bry. Following VSLS oxidation, bromine radicals (Br and BrO) can catalytically destroy ozone. The extent to which possible increases in surface emissions or transport of these VSLS bromocarbons to the stratosphere could counteract the effect of halogen reductions under the Montreal Protocol is an important policy question. Here, by using a chemistry–climate model, UM-UKCA, we investigate the impact of a hypothetical doubling (an increase of 5 ppt Bry) of VSLS bromocarbons on ozone and how the resulting ozone changes depend on the background concentrations of chlorine and bromine. Our model experiments indicate that for the 5 ppt increase in Bry from VSLS, the ozone decrease in the lowermost stratosphere of the Southern Hemisphere (SH) may reach up to 10% in the annual mean; the ozone decrease in the Northern Hemisphere (NH) is smaller (4–6%). The largest impact on the ozone column is found in the Antarctic spring. There is a significantly larger ozone decrease following the doubling of the VSLS burden under a high stratospheric chlorine background than under a low chlorine background, indicating the importance of the inter-halogen reactions. For example, the decline in the high-latitude, lower-stratospheric ozone concentration as a function of Bry is higher by about 30–40% when stratospheric Cly is ~ 3 ppb (present day), compared with Cly of ~ 0.8 ppb (a pre-industrial or projected future situation). Bromine will play an important role in the future ozone layer. However, even if bromine levels from natural VSLS were to increase significantly later this century, changes in the concentration of ozone will likely be dominated by the decrease in anthropogenic chlorine. Our calculation suggests that for a 5 ppt increase in Bry from VSLS, the Antarctic ozone hole recovery date could be delayed by approximately 6–8 years, depending on Cly levels.


Science ◽  
2013 ◽  
Vol 339 (6119) ◽  
pp. 568-570 ◽  
Author(s):  
Darryn W. Waugh ◽  
Francois Primeau ◽  
Tim DeVries ◽  
Mark Holzer

Surface westerly winds in the Southern Hemisphere have intensified over the past few decades, primarily in response to the formation of the Antarctic ozone hole, and there is intense debate on the impact of this on the ocean's circulation and uptake and redistribution of atmospheric gases. We used measurements of chlorofluorocarbon-12 (CFC-12) made in the southern oceans in the early 1990s and mid- to late 2000s to examine changes in ocean ventilation. Our analysis of the CFC-12 data reveals a decrease in the age of subtropical subantarctic mode waters and an increase in the age of circumpolar deep waters, suggesting that the formation of the Antarctic ozone hole has caused large-scale coherent changes in the ventilation of the southern oceans.


2017 ◽  
Author(s):  
Sweta Shah ◽  
Olaf Tuinder ◽  
Jacob van Peet ◽  
Adrianus de Laat ◽  
Piet Stammes

Abstract. The depletion of the Antarctic ozone layer and its changing vertical distribution has been monitored closely by satellites in the past decades ever since the Antarctic ozone hole was discovered in the 1980's. Ozone profile retrieval from nadir-viewing satellites operating in the ultraviolet-visible range requires accurate calibration of level-1 (L1) radiance data. Here we study the effects of calibration on the derived level-2 (L2) ozone profiles and apply the retrieval to the Antarctic ozone hole region. We retrieve nadir ozone profiles from the SCIAMACHY instrument that flew on-board Envisat using the Ozone ProfilE Retrieval Algorithm) (OPERA) developed at KNMI with a focus on the stratospheric ozone. We study and assess the quality of these profiles and compare retrieved (L2) products from L1 SCIAMACHY versions 7 and 8 indicated as respectively (v7, v8) data from the years 2003–2011 without further radiometric correction. From validation of the profiles against ozone sonde measurements, we find that the v8 performs better due to correction for the scan-angle dependency of the instrument's optical degradation. The instrument spectral response function can still be improved for the L1 v8 data with a shift and squeeze. We find that the contribution from this improvement is a few percent residue reduction compared to a reference in the solar irradiance spectra. Validation for the years 2003 and 2009 with ozone sondes shows deviations of SCIAMACHY ozone profiles of 0.8 %–15 % in the stratosphere and 2.5 %–100 % in the troposphere, depending on the latitude and the L1 version used. Using L1 v8 for the years 2003–2011 leads to deviations of ~ 1 %–11 % in stratospheric ozone and ~ 1 %–45 % in tropospheric ozone. Application of SCIAMACHY v8 data on the Antarctic ozone hole shows that most ozone is depleted in the latitude range from 70° S to 90° S. The minimum integrated ozone column consistently occurs around 15 September for the years 2003–2011. Furthermore from the ozone profiles for all these years we observe that the value of ozone column per layer reduces to almost zero at a pressure of 100 hPa in the latitude range of 70° S to 90° S, as was found from other observations.


2019 ◽  
Vol 69 (1) ◽  
pp. 29
Author(s):  
Andrew R. Klekociuk ◽  
Matthew B. Tully ◽  
Paul B. Krummel ◽  
Oleksandr Evtushevsky ◽  
Volodymyr Kravchenko ◽  
...  

We review the 2017 Antarctic ozone hole, making use of various meteorological reanalyses, and in-situ, satellite and ground-based measurements of ozone and related trace gases, and ground-based measurements of ultraviolet radiation. The 2017 ozone hole was associated with relatively high-ozone concentrations over the Antarctic region compared to other years, and our analysis ranked it in the smallest 25% of observed ozone holes in terms of size. The severity of stratospheric ozone loss was comparable with that which occurred in 2002 (when the stratospheric vortex exhibited an unprecedented major warming) and most years prior to 1989 (which were early in the development of the ozone hole). Disturbances to the polar vortex in August and September that were associated with intervals of anomalous planetary wave activity resulted in significant erosion of the polar vortex and the mitigation of the overall level of ozone depletion. The enhanced wave activity was favoured by below-average westerly winds at high southern latitudes during winter, and the prevailing easterly phase of the quasi-biennial oscillation (QBO). Using proxy information on the chemical make-up of the polar vortex based on the analysis of nitrous oxide and the likely influence of the QBO, we suggest that the concentration of inorganic chlorine, which plays a key role in ozone loss, was likely similar to that in 2014 and 2016, when the ozone hole was larger than that in 2017. Finally, we found that the overall severity of Antarctic ozone loss in 2017 was largely dictated by the timing of the disturbances to the polar vortex rather than interannual variability in the level of inorganic chlorine.


2014 ◽  
Vol 14 (7) ◽  
pp. 9729-9745 ◽  
Author(s):  
X. Yang ◽  
N. L. Abraham ◽  
A. T. Archibald ◽  
P. Braesicke ◽  
J. Keeble ◽  
...  

Abstract. Naturally produced very short-lived substances (VSLS), like bromocarbons, account for almost a quarter of the current stratospheric inorganic bromine, Bry. Following VSLS oxidation, bromine radicals (Br and BrO) can catalytically destroy ozone. The extent to which possible increases in surface emissions or transport of these VSLS bromocarbons to the stratosphere could counteract the effect of halogen reductions under the Montreal Protocol is an important policy question. Here by using a chemistry–climate model, UM-UKCA, we investigate the impact of a hypothetical increase in VSLS on ozone and how that impact depends on the background concentrations of chlorine and bromine. Our model experiments indicate that for a ~5 ppt increase in Bry from VSLS, the local ozone loss in the lowermost stratosphere of the Southern Hemisphere (SH) may reach up to 10% in the annual mean; the ozone loss in the Northern Hemisphere (NH) is smaller (4–6%). There is more ozone loss following an increase in VSLS burden under a high stratospheric chlorine background than under a low chlorine background indicating the importance of the inter-halogen reactions. For example, the rate of decline of the stratospheric ozone concentration as a function of Bry is higher by about 30–40% when stratospheric Cly is ~3 ppb (present day) compared with Cly of ~0.8 ppb (apre-industrial or projected future situation). Although bromine plays an important role in destroying ozone, inorganic chlorine is the dominant halogen compound. Even if bromine levels from natural VSLS were to increase significantly later this century, changes in the concentration of ozone will be dominated by the recovery of anthropogenic chlorine. Our calculation suggests that for a 5 ppt increase in Bry from VSLS, the Antarctic ozone hole recover date could be delayed by approximately 7 years.


1988 ◽  
Vol 15 (2) ◽  
pp. 101-115 ◽  
Author(s):  
F. Sherwood Rowland

The momentous subject of chlorofluorocarbons (CFCs) and their effect on The Biosphere's stratospheric ozone shield is treated rather generally but in sufficient depth where necessary in three main sections dealing with (i) scientific background and current status of ongoing investigation, (ii) the major technological uses of CFCs and available or foreseeable alternatives to them, and (iii) the policy status and regulatory activity involving present or proposed future restrictions in CFC emissions.It being unlikely that life, at least as we know it, would have developed on Earth without an ozone layer in the stratosphere to ‘filter off’ harmful ultraviolet rays from solar radiation, the prospect of continuing manufacture in developing countries of its destroyers is highly alarming, especially as these destructive CFCs may take more than a decade from emission to reach the levels around 40 km altitude at which they do the most harm.


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