scholarly journals Variations in Ozone Concentration over the Mid-Latitude Region Revealed by Ozonesonde Observations in Pohang, South Korea

Atmosphere ◽  
2020 ◽  
Vol 11 (7) ◽  
pp. 746 ◽  
Author(s):  
Daegeun Shin ◽  
Seungjoo Song ◽  
Sang-Boom Ryoo ◽  
Sang-Sam Lee

Ozone absorbs harmful UV rays at high elevations but acts as a pollutant gas in the lower atmosphere. It is necessary to monitor both the vertical profile and the total column ozone. In this study, variations in the ozone concentration of Pohang were divided into three vertical layers: the stratospheric layer (STL), the second ozone peak layer (SOPL), and the tropospheric layer (TRL). Our results indicated that the ozone concentration in the STL, SOPL, TRL, and total column ozone increased by 0.45%, 2.64%, 5.26%, and 1.07% decade−1, respectively. The increase in the SOPL during springtime indicates that stratosphere–troposphere exchange is accelerating, while the increase during summertime appears to have been influenced by the lower layers. The growth of tropospheric ozone concentration is the result of both increased ozone precursors from industrialization in East Asia and the influx of stratospheric ozone. Our results reaffirmed the trend of ozone concentration in mid-latitudes of the northern hemisphere from vertical profiles in Pohang and, in particular, suggests that the recent changes of ozone in this region need to be carefully monitored.

2007 ◽  
Vol 25 (11) ◽  
pp. 2321-2334 ◽  
Author(s):  
V. Sivakumar ◽  
T. Portafaix ◽  
H. Bencherif ◽  
S. Godin-Beekmann ◽  
S. Baldy

Abstract. The study presents the climatological characteristics of stratospheric ozone observed over Reunion Island using in-situ (ozonesonde and SAOZ) and satellite (UARS-HALOE, SAGE-II and TOMS) measurements. It uses co-localised ozonesondes (from September 1992 to February 2005) and SAOZ measurements (from January 1993 to December 2004), SAGE-II data from October 1984 to February 1999 (~15 years), HALOE data from January 1991 to February 2005 (~15 years), and NIMBUS/TOMS data from January 1978 to December 2004 (27 years). The satellite measurements correspond to overpasses located nearby Reunion Island (21° S; 55° E). The height profiles of ozone concentration obtained from ozonesonde (0.5–29.5 km) show less bias in comparison with the HALOE and SAGE-II measurements. Though, the satellite (HALOE and SAGE-II) measurements underestimate the tropospheric ozone, they are in good agreement for the heights above 15 km. The bias between the measurements and the normalized ozone profile constructed from the ozonesonde and SAGE-II satellite measurement shows that the SAGE-II measurements are more accurate than the HALOE measurements in the lower stratosphere. The monthly variation of ozone concentration derived from ozonesonde and HALOE shows a nearly annual cycle with a maximum concentration during winter/spring and minimum concentration during summer/autumn months. The time evolution of total column ozone obtained from TOMS, SAOZ and the one computed from ozonesonde and SAGE-II, exhibits similar behaviour with analogous trends as above. The TOMS variation displays a higher value of total column ozone of about 3–5 DU (10%) in comparison with the SAOZ and the integrated ozone from ozonesonde and SAGE-II.


Atmosphere ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 112
Author(s):  
Lin Shang ◽  
Jiali Luo ◽  
Chunxiao Wang

This study compares and analyzes simulations of ozone under different scenarios by three CMIP6 models (IPSL-CM6A, MRI-ESM2 and CESM-WACCM). Results indicate that as the social vulnerability and anthropogenic radiative forcing is increasing, the change of total column ozone in the tropical stratosphere is not linear. Compared to the SSP2-4.5 and SSP5-8.5 scenarios, the SSP1-2.6 and SSP3-7.0 are more favorable for the increase in stratospheric ozone mass in the tropics. Arctic ozone would never recover under the SSP1-2.6 scenario; however, the Antarctica ozone would gradually recover in all scenarios. Under the SSP1-2.6 and SSP2-4.5 scenarios, the trend of tropical total column ozone is mainly determined by the trend of column ozone in the tropical troposphere. Under the SSP3-7.0 scenario, tropospheric ozone concentration will significantly increase; under the SSP5-8.5 scenario, ozone concentration will distinctly increase in the middle and lower troposphere.


2018 ◽  
Author(s):  
Richard McPeters ◽  
Stacey Frith ◽  
Natalya Kramarova ◽  
Jerry Ziemke ◽  
Gordon Labow

Abstract. A version 2 processing of data from two ozone monitoring instruments on Suomi NPP, the OMPS nadir ozone mapper and the OMPS nadir ozone profiler, has now been completed. The previously released data were useful for many purposes but were not suitable for use in ozone trend analysis. In this processing, instrument artifacts have been identified and corrected, an improved scattered light correction and wavelength registration have been applied, and soft calibration techniques were implemented to produce a calibration consistent with data from the series of SBUV/2 instruments. The result is a high quality ozone time series suitable for trend analysis. Total column ozone data from the OMPS nadir mapper now agree with data from the SBUV/2 instrument on NOAA 19 with a zonal average bias of −0.2 % over the 60° S to 60° N latitude zone. Differences are somewhat larger between OMPS nadir profiler and N19 total column ozone, with an average difference of −1.1  % over the 60° S to 60° N latitude zone and a residual seasonal variation of about 2 % at latitudes higher than about 50 degrees. For the profile retrieval, zonal average ozone in the upper stratosphere (between 2.5 and 4 hPa) agrees with that from NOAA 19 within ±3 % and an average bias of −1.1 %. In the lower stratosphere (between 25 and 40 hPa) agreement is within ±3 % with an average bias of +1.1 %. Tropospheric ozone produced by subtracting stratospheric ozone measured by the OMPS limb profiler from total column ozone measured by the nadir mapper is consistent with tropospheric ozone produced by subtracting stratospheric ozone from MLS from total ozone from the OMI instrument on Aura. The agreement of tropospheric ozone is within 10 % in most locations.


2016 ◽  
Author(s):  
E. M. Bednarz ◽  
A. C. Maycock ◽  
N. L. Abraham ◽  
P. Braesicke ◽  
O. Dessens ◽  
...  

Abstract. Future trends in Arctic springtime total column ozone, and its chemical and dynamical drivers, are assessed using a 7 member ensemble from the Met Office Unified Model with United Kingdom Chemistry and Aerosols (UM-UKCA) simulating the period 1960-2100. The Arctic mean March total column ozone increases throughout the 21st century at a rate of ~11.5 DU decade-1, and is projected to return to the 1980 level in the late 2030s. However, the integrations show that even past 2060 springtime Arctic ozone can episodically drop by ~50-100 DU below the long-term mean to near present day values. Consistent with the global decline in inorganic chlorine (Cly) over the century, the estimated mean halogen induced chemical ozone loss in the Arctic lower atmosphere in spring decreases by around a factor of two between 1981-2000 and 2061-2080. However, in the presence of a cold and strong polar vortex elevated halogen losses well above the long-term mean continue to occur in the simulations into the second part of the century. The ensemble shows a radiatively-driven cooling trend modelled in the Arctic winter mid- and upper stratosphere, but there is less consistency across the seven ensemble members in the lower stratosphere (100-50 hPa). This is partly due to an increase in downwelling over the Arctic polar cap in winter, which increases transport of ozone into the polar region as well as drives adiabatic warming that partly offsets the radiatively-driven stratospheric cooling. However, individual years characterised by significantly suppressed downwelling, reduced transport and low temperatures continue into the future. We conclude that despite the future long-term recovery of Arctic ozone, the large interannual dynamical variability is expected to continue thereby facilitating episodic reductions in springtime ozone columns. Whilst our results suggest that the relative role of dynamical processes for determining Arctic springtime ozone will increase in the future, halogen chemistry will remain a smaller but non-negligible contributor for many decades.


2013 ◽  
Vol 13 (3) ◽  
pp. 7081-7112 ◽  
Author(s):  
P. J. Nair ◽  
S. Godin-Beekmann ◽  
J. Kuttippurath ◽  
G. Ancellet ◽  
F. Goutail ◽  
...  

Abstract. The trends and variability of ozone are assessed over a northern mid-latitude station, Haute-Provence Observatory (OHP – 43.93° N, 5.71° E), using total column ozone observations from the Dobson and Système d'Analyse par Observation Zénithale spectrometers, and stratospheric ozone profile measurements from Light detection and ranging, ozonesondes, Stratospheric Aerosol and Gas Experiment II, Halogen Occultation Experiment and Aura Microwave Limb Sounder. A multi-variate regression model with quasi biennial oscillation (QBO), solar flux, aerosol optical thickness, heat flux, North Atlantic oscillation (NAO) and piecewise linear trend (PWLT) or Equivalent Effective Stratospheric Chlorine (EESC) functions is applied to the ozone anomalies. The maximum variability of ozone in winter/spring is explained by QBO and heat flux in 15–45 km and in 15–24 km, respectively. The NAO shows maximum influence in the lower stratosphere during winter while the solar flux influence is largest in the lower and middle stratosphere in summer. The total column ozone trends estimated from the PWLT and EESC functions are of −1.39±0.26 and −1.40±0.25 DU yr−1, respectively over 1984–1996 and about 0.65±0.32 and 0.42±0.08 DU yr−1, respectively over 1997–2010. The ozone profiles yield similar and significant EESC-based and PWLT trends in 1984–1996 and are about −0.5 and −0.8 % yr−1 in the lower and upper stratosphere, respectively. In 1997–2010, the EESC-based and PWLT trends are significant and of order 0.3 and 0.1 % yr−1, respectively in the 18–28 km range, and at 40–45 km, EESC provides significant ozone trends larger than the insignificant PWLT results. Therefore, this analysis unveils ozone recovery signals from total column ozone and profile measurements at OHP, and hence in the mid-latitudes.


2018 ◽  
Vol 18 (2) ◽  
pp. 1379-1394 ◽  
Author(s):  
William T. Ball ◽  
Justin Alsing ◽  
Daniel J. Mortlock ◽  
Johannes Staehelin ◽  
Joanna D. Haigh ◽  
...  

Abstract. Ozone forms in the Earth's atmosphere from the photodissociation of molecular oxygen, primarily in the tropical stratosphere. It is then transported to the extratropics by the Brewer–Dobson circulation (BDC), forming a protective ozone layer around the globe. Human emissions of halogen-containing ozone-depleting substances (hODSs) led to a decline in stratospheric ozone until they were banned by the Montreal Protocol, and since 1998 ozone in the upper stratosphere is rising again, likely the recovery from halogen-induced losses. Total column measurements of ozone between the Earth's surface and the top of the atmosphere indicate that the ozone layer has stopped declining across the globe, but no clear increase has been observed at latitudes between 60° S and 60° N outside the polar regions (60–90°). Here we report evidence from multiple satellite measurements that ozone in the lower stratosphere between 60° S and 60° N has indeed continued to decline since 1998. We find that, even though upper stratospheric ozone is recovering, the continuing downward trend in the lower stratosphere prevails, resulting in a downward trend in stratospheric column ozone between 60° S and 60° N. We find that total column ozone between 60° S and 60° N appears not to have decreased only because of increases in tropospheric column ozone that compensate for the stratospheric decreases. The reasons for the continued reduction of lower stratospheric ozone are not clear; models do not reproduce these trends, and thus the causes now urgently need to be established.


2013 ◽  
Vol 13 (20) ◽  
pp. 10373-10384 ◽  
Author(s):  
P. J. Nair ◽  
S. Godin-Beekmann ◽  
J. Kuttippurath ◽  
G. Ancellet ◽  
F. Goutail ◽  
...  

Abstract. The trends and variability of ozone are assessed over a northern mid-latitude station, Haute-Provence Observatory (OHP: 43.93° N, 5.71° E), using total column ozone observations from the Dobson and Système d'Analyse par Observation Zénithale spectrometers, and stratospheric ozone profile measurements from light detection and ranging (lidar), ozonesondes, Stratospheric Aerosol and Gas Experiment (SAGE) II, Halogen Occultation Experiment (HALOE) and Aura Microwave Limb Sounder (MLS). A multivariate regression model with quasi-biennial oscillation (QBO), solar flux, aerosol optical thickness, heat flux, North Atlantic Oscillation (NAO) and a piecewise linear trend (PWLT) or equivalent effective stratospheric chlorine (EESC) functions is applied to the ozone anomalies. The maximum variability of ozone in winter/spring is explained by QBO and heat flux in the ranges 15–45 km and 15–24 km, respectively. The NAO shows maximum influence in the lower stratosphere during winter, while the solar flux influence is largest in the lower and middle stratosphere in summer. The total column ozone trends estimated from the PWLT and EESC functions are of −1.47 ± 0.27 and −1.40 ± 0.25 DU yr−1, respectively, over the period 1984–1996 and about 0.55 ± 0.30 and 0.42 ± 0.08 DU yr−1, respectively, over the period 1997–2010. The ozone profiles yield similar and significant EESC-based and PWLT trends for 1984–1996, and are about −0.5 and −0.8% yr−1 in the lower and upper stratosphere, respectively. For 1997–2010, the EESC-based and PWLT estimates are of the order of 0.3 and 0.1% yr−1, respectively, in the 18–28 km range, and at 40–45 km, EESC provides significant ozone trends larger than the insignificant PWLT results. Furthermore, very similar vertical trends for the respective time periods are also deduced from another long-term satellite-based data set (GOZCARDS–Global OZone Chemistry And Related trace gas Data records for the Stratosphere) sampled at northern mid-latitudes. Therefore, this analysis unveils ozone recovery signals from total column ozone and profile measurements at OHP, and hence in the northern mid-latitudes.


2013 ◽  
Vol 6 (10) ◽  
pp. 2533-2548 ◽  
Author(s):  
P. K. Bhartia ◽  
R. D. McPeters ◽  
L. E. Flynn ◽  
S. Taylor ◽  
N. A. Kramarova ◽  
...  

Abstract. We describe the algorithm that has been applied to develop a 42 yr record of total ozone and ozone profiles from eight Solar Backscatter UV (SBUV) instruments launched on NASA and NOAA satellites since April 1970. The Version 8 (V8) algorithm was released more than a decade ago and has been in use since then at NOAA to produce their operational ozone products. The current algorithm (V8.6) is basically the same as V8, except for updates to instrument calibration, incorporation of new ozone absorption cross-sections, and new ozone and cloud height climatologies. Since the V8 algorithm has been optimized for deriving monthly zonal mean (MZM) anomalies for ozone assessment and model comparisons, our emphasis in this paper is primarily on characterizing the sources of errors that are relevant for such studies. When data are analyzed this way the effect of some errors, such as vertical smoothing of short-term variability, and noise due to clouds and aerosols diminish in importance, while the importance of others, such as errors due to vertical smoothing of the quasi-biennial oscillation (QBO) and other periodic and aperiodic variations, become more important. With V8.6 zonal mean data we now provide smoothing kernels that can be used to compare anomalies in SBUV profile and partial ozone columns with models. In this paper we show how to use these kernels to compare SBUV data with Microwave Limb Sounder (MLS) ozone profiles. These kernels are particularly useful for comparisons in the lower stratosphere where SBUV profiles have poor vertical resolution but partial column ozone values have high accuracy. We also provide our best estimate of the smoothing errors associated with SBUV MZM profiles. Since smoothing errors are the largest source of uncertainty in these profiles, they can be treated as error bars in deriving interannual variability and trends using SBUV data and for comparing with other measurements. In the V8 and V8.6 algorithms we derive total column ozone by integrating the SBUV profiles, rather than from a separate set of wavelengths, as was done in previous algorithm versions. This allows us to extend the total ozone retrieval to 88° solar zenith angle (SZA). Since the quality of total column data is affected by reduced sensitivity to ozone in the lower atmosphere by cloud and Rayleigh attenuation, which gets worse with increasing SZA, we provide our best estimate of these errors, as well as the kernels that can be used to test the sensitivity of the derived columns to long-term changes in ozone in the lower atmosphere.


2010 ◽  
Vol 10 (19) ◽  
pp. 9451-9472 ◽  
Author(s):  
V. Eyring ◽  
I. Cionni ◽  
G. E. Bodeker ◽  
A. J. Charlton-Perez ◽  
D. E. Kinnison ◽  
...  

Abstract. Projections of stratospheric ozone from a suite of chemistry-climate models (CCMs) have been analyzed. In addition to a reference simulation where anthropogenic halogenated ozone depleting substances (ODSs) and greenhouse gases (GHGs) vary with time, sensitivity simulations with either ODS or GHG concentrations fixed at 1960 levels were performed to disaggregate the drivers of projected ozone changes. These simulations were also used to assess the two distinct milestones of ozone returning to historical values (ozone return dates) and ozone no longer being influenced by ODSs (full ozone recovery). The date of ozone returning to historical values does not indicate complete recovery from ODSs in most cases, because GHG-induced changes accelerate or decelerate ozone changes in many regions. In the upper stratosphere where CO2-induced stratospheric cooling increases ozone, full ozone recovery is projected to not likely have occurred by 2100 even though ozone returns to its 1980 or even 1960 levels well before (~2025 and 2040, respectively). In contrast, in the tropical lower stratosphere ozone decreases continuously from 1960 to 2100 due to projected increases in tropical upwelling, while by around 2040 it is already very likely that full recovery from the effects of ODSs has occurred, although ODS concentrations are still elevated by this date. In the midlatitude lower stratosphere the evolution differs from that in the tropics, and rather than a steady decrease in ozone, first a decrease in ozone is simulated from 1960 to 2000, which is then followed by a steady increase through the 21st century. Ozone in the midlatitude lower stratosphere returns to 1980 levels by ~2045 in the Northern Hemisphere (NH) and by ~2055 in the Southern Hemisphere (SH), and full ozone recovery is likely reached by 2100 in both hemispheres. Overall, in all regions except the tropical lower stratosphere, full ozone recovery from ODSs occurs significantly later than the return of total column ozone to its 1980 level. The latest return of total column ozone is projected to occur over Antarctica (~2045–2060) whereas it is not likely that full ozone recovery is reached by the end of the 21st century in this region. Arctic total column ozone is projected to return to 1980 levels well before polar stratospheric halogen loading does so (~2025–2030 for total column ozone, cf. 2050–2070 for Cly+60×Bry) and it is likely that full recovery of total column ozone from the effects of ODSs has occurred by ~2035. In contrast to the Antarctic, by 2100 Arctic total column ozone is projected to be above 1960 levels, but not in the fixed GHG simulation, indicating that climate change plays a significant role.


2016 ◽  
Vol 16 (18) ◽  
pp. 12159-12176 ◽  
Author(s):  
Ewa M. Bednarz ◽  
Amanda C. Maycock ◽  
N. Luke Abraham ◽  
Peter Braesicke ◽  
Olivier Dessens ◽  
...  

Abstract. Future trends in Arctic springtime total column ozone, and its chemical and dynamical drivers, are assessed using a seven-member ensemble from the Met Office Unified Model with United Kingdom Chemistry and Aerosols (UM-UKCA) simulating the period 1960–2100. The Arctic mean March total column ozone increases throughout the 21st century at a rate of  ∼  11.5 DU decade−1, and is projected to return to the 1980 level in the late 2030s. However, the integrations show that even past 2060 springtime Arctic ozone can episodically drop by  ∼  50–100 DU below the corresponding long-term ensemble mean for that period, reaching values characteristic of the near-present-day average level. Consistent with the global decline in inorganic chlorine (Cly) over the century, the estimated mean halogen-induced chemical ozone loss in the Arctic lower atmosphere in spring decreases by around a factor of 2 between the periods 2001–2020 and 2061–2080. However, in the presence of a cold and strong polar vortex, elevated halogen-induced ozone losses well above the corresponding long-term mean continue to occur in the simulations into the second part of the century. The ensemble shows a significant cooling trend in the Arctic winter mid- and upper stratosphere, but there is less confidence in the projected temperature trends in the lower stratosphere (100–50 hPa). This is partly due to an increase in downwelling over the Arctic polar cap in winter, which increases transport of ozone into the polar region as well as drives adiabatic warming that partly offsets the radiatively driven stratospheric cooling. However, individual winters characterised by significantly suppressed downwelling, reduced transport and anomalously low temperatures continue to occur in the future. We conclude that, despite the projected long-term recovery of Arctic ozone, the large interannual dynamical variability is expected to continue in the future, thereby facilitating episodic reductions in springtime ozone columns. Whilst our results suggest that the relative role of dynamical processes for determining Arctic springtime ozone will increase in the future, halogen chemistry will remain a smaller but non-negligible contributor for many decades to come.


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