Dobson Units Research Articles

Record High March 2024 Arctic Total Column Ozone

AbstractObservations of March 2024 Arctic (63°N–90°N) total column ozone set a record high of 477 Dobson Units (DU) against the 1979–2023 satellite era time series. It was about 60 DU higher than average and 6 DU higher than the previous March 1979 471 DU record. Daily Arctic ozone was above average for every day in March 2024, and set record highs from 11–26 March 2024. Microwave Limb Sounder data show this record ozone anomaly was concentrated in the lower stratosphere (10–30 km). These record values developed over the 2023–2024 winter and can be associated with vertically propagating planetary‐scale wave events that caused significant stratospheric warmings. These wave events forced poleward and downward ozone advection into the lower stratosphere, leading to record column ozone levels. The above average levels persisted through August 2024 and across the northern hemisphere.

Importance of microphysical settings for climate forcing by stratospheric SO2 injections as modeled by SOCOL-AERv2

Abstract. Solar radiation modification by a sustained deliberate source of SO2 into the stratosphere (strat-SRM) has been proposed as an option for climate intervention. Global interactive aerosol–chemistry–climate models are often used to investigate the potential cooling efficiencies and associated side effects of hypothesized strat-SRM scenarios. A recent model intercomparison study for composition–climate models with interactive stratospheric aerosol suggests that the modeled climate response to a particular assumed injection strategy depends on the type of aerosol microphysical scheme used (e.g., modal or sectional representation) alongside host model resolution and transport. Compared to short-duration volcanic SO2 emissions, the continuous SO2 injections in strat-SRM scenarios may pose a greater challenge to the numerical implementation of microphysical processes such as nucleation, condensation, and coagulation. This study explores how changing the time steps and sequencing of microphysical processes in the sectional aerosol–chemistry–climate model SOCOL-AERv2 (40 mass bins) affects model-predicted climate and ozone layer impacts considering strat-SRM by SO2 injections of 5 and 25 Tg(S) yr−1 at 20 km altitude between 30° S and 30° N. The model experiments consider the year 2040 to be the boundary conditions for ozone-depleting substances and greenhouse gases (GHGs). We focus on the length of the microphysical time step and the call sequence of nucleation and condensation, the two competing sink processes for gaseous H2SO4. Under stratospheric background conditions, we find no effect of the microphysical setup on the simulated aerosol properties. However, at the high sulfur loadings reached in the scenarios injecting 25 Tg(S) yr−1 of SO2 with a default microphysical time step of 6 min, changing the call sequence from the default “condensation first” to “nucleation first” leads to a massive increase in the number densities of particles in the nucleation mode (R<0.01 µm) and a small decrease in coarse-mode particles (R>1 µm). As expected, the influence of the call sequence becomes negligible when the microphysical time step is reduced to a few seconds, with the model solutions converging to a size distribution with a pronounced nucleation mode. While the main features and spatial patterns of climate forcing by SO2 injections are not strongly affected by the microphysical configuration, the absolute numbers vary considerably. For the extreme injection with 25 Tg(S) yr−1, the simulated net global radiative forcing ranges from −2.3 to −5.3 W m−2, depending on the microphysical configuration. Nucleation first shifts the size distribution towards radii better suited for solar scattering (0.3 µm <R< 0.4 µm), enhancing the intervention efficiency. The size distribution shift, however, generates more ultrafine aerosol particles, increasing the surface area density and resulting in 10 DU (Dobson units) less ozone (about 3 % of the total column) in the northern mid-latitudes and 20 DU less ozone (6 %) over the polar caps compared to the condensation first approach. Our results suggest that a reasonably short microphysical time step of 2 min or less must be applied to accurately capture the magnitude of the H2SO4 supersaturation resulting from SO2 injection scenarios or volcanic eruptions. Taken together, these results underscore how structural aspects of model representation of aerosol microphysical processes become important under conditions of elevated stratospheric sulfur in determining atmospheric chemistry and climate impacts.

The ozone hole and a phase change in lower stratospheric temperature

Depletion of ozone over Antarctica was first observed in the late 1970s, and discovery of the Antarctic ozone hole was announced in the 1980s as having started in 1979. The ozone hole was defined as the area with total column ozone less than 220 Dobson units. Analysis of ozone, temperature, chlorofluorocarbon and nitrous oxide data from 1963 onwards suggests that the annual ozone minimum at the South Pole is related to lower stratospheric temperature independently of chlorofluorocarbons and nitrous oxide. There were ozone holes, ie. column ozone less than 220 Dobson Units, at the South Pole in several years before 1979 (the date that the ozone hole is reported to have first appeared) when chlorofluorocarbon concentrations were much lower than today and lower than in 1979. An early 1980s phase change in the lower stratospheric temperature at the South Pole at altitudes between 250 hPa and 100 hPa, and at some lower altitudes, coincides with a phase change in the annual South Pole ozone minimum. The phase change is not visible in chlorofluorocarbon or nitrous oxide data. This raises the possibility that, over a multi-annual or decadal timescale, lower stratospheric temperature has more effect than chlorofluorocarbons or nitrous oxide on atmospheric ozone concentration over the South Pole. Alternatively, temperature and ozone may both be reacting to some other influence.

Novel use of an adapted ultraviolet double monochromator for measurements of global and direct irradiance, ozone, and aerosol

Abstract. A novel ultraviolet spectrometer has been developed and tested over 10 years at Lauder, New Zealand. The system, UV2, makes alternating measurements of the global and direct UV irradiance and can therefore be used to measure ozone and aerosol optical depth. After an analysis of the stability of UV2, these measurements, along with UV irradiance, are compared to relevant observations made by an additional UV spectrometer (UV4), a Dobson spectrophotometer (no. 072), and two radiometers measuring aerosol optical depth – a Prede sky radiometer and a Middleton Solar radiometer (SP02). UV2 irradiance is shown to be lower than UV4 by between 2.5 % and 3.5 %, with a standard deviation of a similar magnitude. Total column ozone values are shown to agree with Dobson spectrophotometer values with a mean bias of 2.57 Dobson units (DU) and standard deviation of 1.15 DU when using the direct sun measurements. Aerosol optical depth at 400–412 and 500 nm agrees to within 0.015 and is comparable to the difference between the reference radiometers. Further work is needed, particularly in the radiometric calibration at longer wavelengths, in order to determine if this instrument can supersede or enhance measurements made by the Dobson spectrophotometer or the aerosol radiometers.

Enhancing ozone nowcasting over East Asia using a data-to-data translation approach with observations from a geostationary environment monitoring spectrometer

The degradation of air quality caused by excessive anthropogenic ozone (O3) concentrations negatively affects ecosystems and the atmosphere. To monitor this issue, the Geostationary Environment Monitoring Spectrometer (GEMS) aboard the Geostationary Korea Multi-Purpose Satellite (GK)-2B provides ozone products over Asia-centered circular regions based on the ozone algorithm derived from representative polar-orbit atmospheric environmental satellites. In this study, we developed a few-hour GEMS O3 nowcasting model using data-to-data (D2D) translation with a conditional generative adversarial network. This model is based on hourly GEMS O3 time-series products and can be used to predict ozone concentrations. The D2D model underwent training and testing employing paired input and output datasets of GEMS O3, with data collected from March 22, 2020, to June 21, 2020, and from March 22, 2021, to June 18, 2021, respectively. The resulting D2D ozone nowcasting model was used to determine ozone concentrations in time zones where GEMS O3 products were unavailable. Test results of the D2D model demonstrated excellent statistical scores, including a bias of 2.162 Dobson Units (DU, where 1 DU corresponds to 2.687 × 1016 molecules/cm2), root-mean-square error (RMSE) of 5.606 DU, a correlation coefficient (CC) of 0.994 for 1-h prediction, a bias of 1.421 DU, RMSE of 5.903 DU, and CC of 0.992 for 2-h prediction, and a bias of 1.169 DU, RMSE of 6.797 DU, and CC of 0.988 for 3-h prediction. Despite the dataset pairing and number limitations, the D2D prediction model accurately forecasted GEMS O3 within 3 h in East Asia.

Airborne observation with a low-cost hyperspectral instrument: retrieval of NO2 vertical column densities (VCDs) and the satellite sub-grid variability over industrial point sources

Abstract. High-spatial-resolution NO2 vertical column densities (VCDs) were retrieved from airborne observations using the low-cost hyperspectral imaging sensor (HIS) at three industrial areas (i.e., Chungnam, Jecheon, and Pohang) in South Korea, where point sources (i.e., power plant, petrochemical complex, steel yard, and cement kiln) with significant NO2 emissions are located. An innovative and versatile approach for NO2 VCD retrieval, hereafter referred to as the modified wavelength pair (MWP) method, was developed to overcome the excessively variable radiometric and spectral characteristics of the HIS attributed to the absence of temperature control during the flight. The newly developed MWP method was designed to be insensitive to broadband spectral features, including the spectral dependency of surface and aerosol reflectivity, and can be applied to observations with relatively low spectral resolutions. Moreover, the MWP method can be implemented without requiring precise radiometric calibration of the instrument (i.e., HIS) by utilizing clean-pixel data for non-uniformity corrections and is also less sensitive to the optical properties of the instrument and offers computational cost competitiveness. In the experimental flights using the HIS, NO2 plumes emitted from steel yards were particularly conspicuous among the various NO2 point sources, with peak NO2 VCDs of 2.0 DU (Dobson unit) at Chungnam and 1.8 DU at Pohang. Typical NO2 VCD uncertainties ranged between 0.025–0.075 DU over the land surface and 0.10–0.15 DU over the ocean surface, and the discrepancy can be attributable to the lower signal-to-noise ratio over the ocean and higher sensitivity of the MWP method to surface reflectance uncertainties under low-albedo conditions. The NO2 VCDs retrieved from the HIS with the MWP method showed a good correlation with the collocated Tropospheric Monitoring Instrument (TROPOMI) data (r=0.73, mean absolute error equals 0.106 DU). However, the temporal disparities between the HIS frames and the TROPOMI overpass, their spatial mismatch, and their different observation geometries could limit the correlation. The comparison of TROPOMI and HIS NO2 VCDs further demonstrated that the satellite sub-grid variability could be intensified near the point sources, with more than a 3-fold increase in HIS NO2 VCD variability (e.g., difference between 25th and 75th quantiles) over the TROPOMI footprints with NO2 VCD values exceeding 0.8 DU compared to footprints with NO2 VCD values below 0.6 DU.

Atmospheric impacts of chlorinated very short-lived substances over the recent past – Part 2: Impacts on ozone

Abstract. Depletion of the stratospheric ozone layer remains an ongoing environmental issue, with increasing stratospheric chlorine from very short-lived substances (VSLS) recently emerging as a potential but uncertain threat to its future recovery. Here the impact of chlorinated VSLS (Cl-VSLS) on past ozone is quantified, for the first time, using the UM–UKCA (Unified Model–United Kingdom Chemistry and Aerosol) chemistry-climate model. Model simulations nudged to reanalysis fields show that in the second decade of the 21st century Cl-VSLS reduced total column ozone by, on average, ∼ 2–3 DU (Dobson unit) in the springtime high latitudes and by ∼0.5 DU in the annual mean in the tropics. The largest ozone reductions were simulated in the Arctic in the springs of 2011 and 2020. During the recent cold Arctic winter of 2019/20 Cl-VSLS resulted in local ozone reductions of up to ∼7 % in the lower stratosphere and of ∼7 DU in total column ozone by the end of March. Despite nearly doubling of Cl-VSLS contribution to stratospheric chlorine over the early 21st century, the inclusion of Cl-VSLS in the nudged simulations does not substantially modify the magnitude of the simulated recent ozone trends and, thus, does not help to explain the persistent negative ozone trends that have been observed in the extra-polar lower stratosphere. The free-running simulations, on the other hand, suggest Cl-VSLS-induced amplification of the negative tropical lower-stratospheric ozone trend by ∼20 %, suggesting a potential role of the dynamical feedback from Cl-VSLS-induced chemical ozone loss. Finally, we calculate the ozone depletion potential of dichloromethane, the most abundant Cl-VSLS, at 0.0107. Our results illustrate a so-far modest but nonetheless non-negligible role of Cl-VSLS in contributing to the stratospheric ozone budget over the recent past that if continues could offset some of the gains achieved by the Montreal Protocol.

Record Low Arctic Stratospheric Ozone in Spring 2020: Measurements of Ground-Based Differential Optical Absorption Spectroscopy in Ny-Ålesund during 2017–2021

The Arctic stratospheric ozone depletion event in spring 2020 was the most severe compared with previous years. We retrieved the critical indicator ozone vertical column density (VCD) using zenith scattered light differential optical absorption spectroscopy (ZSL-DOAS) from March 2017 to September 2021 in Ny-Ålesund, Svalbard, Norway. The average ozone VCD over Ny-Ålesund between 18 March and 18 April 2020 was approximately 274.8 Dobson units (DU), which was only 64.7 ± 0.1% of that recorded in other years (2017, 2018, 2019, and 2021). The daily peak difference was 195.7 DU during this period. The retrieved daily averages of ozone VCDs were compared with satellite observations from the Global Ozone Monitoring Experiment-2 (GOME-2), a Brewer spectrophotometer, and a Système d’Analyze par Observation Zénithale (SAOZ) spectrometer at Ny-Ålesund. As determined using the empirical cumulative density function, ozone VCDs from the ZSL-DOAS dataset were strongly correlated with data from the GOME-2 and SAOZ at lower and higher values, and ozone VCDs from the Brewer instrument were overestimated. The resulting Pearson correlation coefficients were relatively high at 0.97, 0.87, and 0.91, respectively. In addition, the relative deviations were 2.3%, 3.1%, and 3.5%, respectively. Sounding and ERA5 data indicated that severe ozone depletion occurred between mid-March and mid-April 2020 in the 16–20 km altitude range over Ny-Ålesund, which was strongly associated with the overall persistently low temperatures in the winter of 2019/2020. Using ZSL-DOAS observations, we obtained ozone VCDs and provided evidence for the unprecedented ozone depletion during the Arctic spring of 2020. This is essential for the study of polar ozone changes and their effect on climate change and ecological conditions.

Potential Impacts on Ozone and Climate From a Proposed Fleet of Supersonic Aircraft

AbstractThere has been renewed interest in developing commercial supersonic transport aircraft due to the increased overall demands by the public for air travel, the aspiration for more intercontinental travel, and the desire for shorter flight times. Various companies and academic institutions have been actively considering the designs of such supersonic aircraft. As these new designs are developed, the environmental impact on ozone and climate of these fleets need to be explored. This study examines one such proposed commercial supersonic fleet of 55‐seater that is projected to fly at Mach 2.2, corresponding to cruise altitudes of 17–20 km, and which would burn 122.32 Tg of fuel and emit 1.78 Tg of NOx each year. Our analyses indicate this proposed fleet would cause a 0.74% reduction in global column ozone (∼2 Dobson Units), which is mainly attributed to the large amounts of nitrogen oxides released in the atmosphere from the supersonic aircraft. The maximum ozone loss occurs at the tropics in the fall season, with a reduction of −1.4% in the total column ozone regionally. The stratospheric‐adjusted radiative forcing on climate from this fleet was derived based on changes in atmospheric concentrations of ozone (59.5 mW/m2), water vapor (10.1 mW/m2), black carbon (−3.9 mW/m2) and sulfate aerosols (−20.3 mW/m2), resulting in a net non‐CO2, non‐contrail forcing of 45.4 mW/m2, indicating an overall warming effect.

South Pole Station ozonesondes: variability and trends in the springtime Antarctic ozone hole 1986–2021

Abstract. Balloon-borne ozonesondes launched weekly from South Pole Station (1986–2021) measure high-vertical-resolution profiles of ozone and temperature from the surface to 30–35 km altitude. The launch frequency is increased in late winter before the onset of rapid stratospheric ozone loss in September. Ozone hole metrics show that the yearly total column ozone and 14–21 km partial column ozone minimum values and September loss rate trends have been improving (less severe) since 2001. The 36-year record also shows interannual variability, especially in recent years (2019–2021). Here we show additional details of these 3 years by comparing annual minimum profiles observed on the date when the lowest integrated total column ozone occurs. We also compare the July–December time series of the 14–21 km partial column ozone values to the 36-year median with percentile intervals. The 2019 anomalous vortex breakdown showed stratospheric temperatures began warming in early September followed by reduced ozone loss. The minimum total column ozone of 180 Dobson units (DU) was observed on 24 September. This was followed by two stable and cold polar vortex years during 2020 and 2021 with total column ozone minimums at 104 DU (1 October) and 102 DU (7 October), respectively. These years also showed broad near-zero-ozone (loss saturation) regions within the 14–21 km layer by the end of September which persisted into October. Validation of the ozonesonde observations is conducted through the ongoing comparison of total column ozone measurements with the South Pole ground-based Dobson spectrophotometer. The ozonesondes show a more positive bias of 2 ± 3 % (higher) than the Dobson following a thorough evaluation and homogenization of the long-term ozonesonde record completed in 2018.

Regional transportation and influence of atmospheric aerosols triggered by Tonga volcanic eruption

A cataclysmic submarine volcano at Hunga Tonga-HungaHa'apai (HTHH) near Tonga, erupted violently on 15 January 2022, which injected a plume of ash cloud soaring into the upper atmosphere. In this study, we examined the regional transportation and potential influence of atmospheric aerosols triggered by HTHH volcano, based on active and passive satellite products, ground-based observations, multi-source reanalysis datasets and atmospheric radiative transfer model. The results indicated that about 0.7 Tg (1 Tg = 109 kg) sulfur dioxide (SO2) gas were emitted into stratosphere from the HTHH volcano, and were lifted to an altitude of 30 km. The regional averaged SO2 columnar content over the western Tonga increased by 10–36 Dobson Units (DU), and the mean aerosol optical thickness (AOT) retrieved from satellite products increased to 0.25–0.34. The stratospheric AOT values caused by HTHH emissions increased to 0.03, 0.20, and 0.23 on 16, 17, and 19 January, respectively, accounting for 1.5%, 21.9%, and 31.1% of total AOT. Ground-based observations also showed an AOT increase of 0.25–0.43, with the maximum daily average of 0.46–0.71 appeared on 17 January. The volcanic aerosols were remarkably dominated by fine-mode particles and posed strong light-scattering and hygroscopic abilities. Consequently, the mean downward surface net shortwave radiative flux was reduced by 2.45–11.9 Wm-2 on different regional scales, and the surface temperature decreased by 0.16–0.42 K. The maximum aerosol extinction coefficient was 0.51 km−1 appeared at 27 km, which resulted in an instantaneous shortwave heating rate of 1.80 Khour−1. These volcanic materials stayed stable in the stratosphere and completed one circle around the earth within 15 days. This would exert a profound influence on the energy budget, water vapor and ozone exchange in the stratosphere, which deserves to be further studied.

Two Air Quality Regimes in Total Column NO2 Over the Gulf of Mexico in May 2019: Shipboard and Satellite Views

AbstractThe Satellite Coastal and Oceanic Atmospheric Pollution Experiment (SCOAPE) cruise in the Gulf of Mexico was conducted in May 2019 by NASA and the Bureau of Ocean Energy Management to determine the feasibility of using satellite data to measure air quality in a region of concentrated oil and natural gas (ONG) operations. SCOAPE addressed both technological and scientific issues related to measuring NO2 columns over the outer continental shelf. Featured were nitrogen dioxide (NO2) instruments (Pandora, Teledyne API analyzer) at Cocodrie, LA (29.26°, −90.66°), and on the Research Vessel Point Sur operating off the Louisiana coast with measurements of ozone, carbon monoxide, and volatile organic compounds (VOCs). The findings: (a) all NO2 observations revealed two atmospheric regimes over the Gulf, the first influenced by tropical air in 10–14 May, the second influenced by flow from urban areas on 15–17 May; (b) comparisons of OMI v4 and TROPOMI v1.3 TC (total column) NO2 data with shipboard Pandora NO2 column observations averaged 13% agreement with the largest difference during 15–17 May (∼20%). At Cocodrie, the satellite–Pandora agreement was ∼5%. (c) Three new‐model Pandora instruments displayed a TC NO2 precision of 0.01 Dobson Units (∼5%); (d) regions of smaller, older natural gas operations showed high methane readings from leakage; elevated VOCs were also detected. Neither satellite nor spectrometer captured the magnitude of ambient NO2 variability near ONG platforms. Given an absence of regular air quality monitoring over the Gulf of Mexico, SCOAPE data constitute a baseline against which future observations can be compared.

Huge Role of Bees in the Biosphere: Philosophical Analyze

In this article, the question of the natural-ecological standard of bees is highlighted, and practical ways of preserving life indicators of the biosphere are shown on its example. Also, in the article, it is proved through examples that the material foundation of the world order, green economy, lies in the ecological standards of the existence of nature. Currently, there are about 8 billion people living in the world. More than 1.1 billion of this population live in an ecologically dangerous environment. Today, one-third of the world’s population lacks clean drinking water. As long as humanity does not comply with the standards and laws of nature in terms of its behavior, labor activities, and impact on nature, it is not a question that it will become not only nature, the environment, but even itself. In order for humanity to live a healthy life on planet Earth, the ozone layer in the biosphere should not decrease below its natural-ecological norm of 300 Dobson units, clean water should not lose its quality indicators, the amount of carbon dioxide in the air should not exceed 0.003%, the biological productivity of water ecosystems should not decrease, the limitric indicators of the soil, ecological values of ecological components should be preserved, pollution and man-made pressures should be reduced.

Ozone depletion in the Arctic and Antarctic stratosphere induced by wildfire smoke

Abstract. A record-breaking stratospheric ozone loss was observed over the Arctic and Antarctica in 2020. Strong ozone depletion occurred over Antarctica in 2021 as well. The ozone holes developed in smoke-polluted air. In this article, the impact of Siberian and Australian wildfire smoke (dominated by organic aerosol) on the extraordinarily strong ozone reduction is discussed. The study is based on aerosol lidar observations in the North Pole region (October 2019–May 2020) and over Punta Arenas in southern Chile at 53.2∘ S (January 2020–November 2021) as well as on respective NDACC (Network for the Detection of Atmospheric Composition Change) ozone profile observations in the Arctic (Ny-Ålesund) and Antarctica (Neumayer and South Pole stations) in 2020 and 2021. We present a conceptual approach on how the smoke may have influenced the formation of polar stratospheric clouds (PSCs), which are of key importance in the ozone-depleting processes. The main results are as follows: (a) the direct impact of wildfire smoke below the PSC height range (at 10–12 km) on ozone reduction seems to be similar to well-known volcanic sulfate aerosol effects. At heights of 10–12 km, smoke particle surface area (SA) concentrations of 5–7 µm2 cm−3 (Antarctica, spring 2021) and 6–10 µm2 cm−3 (Arctic, spring 2020) were correlated with an ozone reduction in terms of ozone partial pressure of 0.4–1.2 mPa (about 30 % further ozone reduction over Antarctica) and of 2–3.5 mPa (Arctic, 20 %–30 % reduction with respect to the long-term springtime mean). (b) Within the PSC height range, we found indications that smoke was able to slightly increase the PSC particle number and surface area concentration. In particular, a smoke-related additional ozone loss of 1–2 mPa (10 %–20 % contribution to the total ozone loss over Antarctica) was observed in the 14–23 km PSC height range in September–October 2020 and 2021. Smoke particle number concentrations ranged from 10 to 100 cm−3 and were about a factor of 10 (in 2020) and 5 (in 2021) above the stratospheric aerosol background level. Satellite observations indicated an additional mean column ozone loss (deviation from the long-term mean) of 26–30 Dobson units (9 %–10 %, September 2020, 2021) and 52–57 Dobson units (17 %–20 %, October 2020, 2021) in the smoke-polluted latitudinal Antarctic belt from 70–80∘ S.

Effects of reanalysis forcing fields on ozone trends and age of air from a chemical transport model

Abstract. We use TOMCAT, a 3-dimensional (3D) offline chemical transport model (CTM) forced by two different meteorological reanalysis data sets (ERA-Interim and ERA5) from the European Centre for Medium-Range weather Forecasts (ECMWF) to analyse seasonal behaviour and long-term trends in stratospheric ozone and mean age of air. The model-simulated ozone variations are evaluated against two observation-based data sets. For total column ozone (TCO) comparisons, we use the Copernicus Climate Change Service (C3S) data (1979–2019), while for ozone profiles we use the Stratospheric Water and OzOne Satellite Homogenized (SWOOSH) data set (1984–2019). We find that the CTM simulations forced by ERA-Interim (A_ERAI) and ERA5 (B_ERA5) can both successfully reproduce the spatial and temporal variations in stratospheric ozone. Also, modelled TCO anomalies from B_ERA5 show better agreement with C3S than A_ERAI, especially in Northern Hemisphere (NH) mid latitudes, except that it gives somewhat larger positive biases (> 15 DU, Dobson units) during winter–spring seasons. Ozone profile comparisons against SWOOSH data show larger differences between the two simulations. In the lower stratosphere, ozone differences can be directly attributed to the representation of dynamical processes, whereas in the upper stratosphere they can be directly linked to the differences in temperatures between ERAI and ERA5 data sets. Although TCO anomalies from B_ERA5 show relatively better agreement with C3S compared to A_ERAI, a comparison with SWOOSH data does not confirm that B_ERA5 performs better at simulating the variations in the stratospheric ozone profiles. We employ a multivariate regression model to quantify the TCO and ozone profile trends before and after peak stratospheric halogen loading in 1997. Our results show that, compared to C3S, TCO recovery trends (since 1998) in simulation B_ERA5 are significantly overestimated in the Southern Hemisphere (SH) mid latitudes, while for A_ERAI in the NH mid latitudes, simulated ozone trends remain negative. Similarly, in the lower stratosphere, B_ERA5 shows positive ozone recovery trends for both NH and SH mid latitudes. In contrast, both SWOOSH and A_ERAI show opposite (negative) trends in the NH mid latitudes. Furthermore, we analyse age of air (AoA) trends to diagnose transport differences between the two reanalysis data sets. Simulation B_ERA5 shows a positive AoA trend after 1998 and somewhat older age in the NH lower stratosphere compared to A_ERAI, indicating that a slower Brewer–Dobson circulation does not translate into reduced wintertime ozone buildup in the NH extratropical lower stratosphere. Overall, our results show that models forced by the most recent ERA5 reanalyses may not yet be capable of reproducing observed changes in stratospheric ozone, particularly in the lower stratosphere.

NASA Satellite Measurements Show Global-Scale Reductions in Free Tropospheric Ozone in 2020 and Again in 2021 During COVID-19.

NASA satellite measurements show that ozone reductions throughout the Northern Hemisphere (NH) free troposphere reported for spring‐summer 2020 during the COronaVIrus Disease 2019 pandemic have occurred again in spring‐summer 2021. The satellite measurements show that tropospheric column ozone (TCO) (mostly representative of the free troposphere) for 20°N–60°N during spring‐summer for both 2020 and 2021 averaged ∼3 Dobson Units (DU) (or ∼7%–8%) below normal. These ozone reductions in 2020 and 2021 were the lowest in the 2005–2021 record. We also include satellite measurements of tropospheric NO2 that exhibit reductions of ∼10%–20% in the NH in early spring‐to‐summer 2020 and 2021, suggesting that reduced pollution was the main cause for the low anomalies in NH TCO in 2020 and 2021. Reductions of TCO ∼2 DU (7%) are also measured in the Southern Hemisphere in austral summer but are not associated with reduced NO2.

Can Column Formaldehyde Observations Inform Air Quality Monitoring Strategies for Ozone and Related Photochemical Oxidants?

AbstractFormaldehyde column density (ΩHCHO) showed a potentially useful correlation with surface ozone during the LISTOS campaign on Long Island Sound and the KORUS‐AQ campaign in Seoul, South Korea. This builds on previous work that identified this relationship from in situ aircraft observations with similar findings for ground‐based and airborne remote sensing of ΩHCHO. In the Long Island Sound region, ΩHCHO and surface ozone exhibited strong temporal (r2 = 0.66) and spatial (r2 = 0.73) correlation. The temporal variability in ΩHCHO (∼1 Dobson units [DU]) was larger than the range in the spatial average (∼0.1 DU). The spatial average is most useful for informing ozone monitoring strategies, demonstrating the challenge in using ΩHCHO satellite data sets for this purpose. In Seoul, high levels of NO2 resulted in Ox better correlating with ΩHCHO than surface ozone due to titration effects. The ΩHCHO–Ox relationship may therefore reflect the sum of surface ozone and related photochemical oxidants, relevant to air quality standards set to regulate this quantity such as the U.S. EPA National Ambient Air Quality Standard (NAAQS). The relationship of ΩHCHO to Ox shifted in Seoul during the campaign demonstrating the need to evaluate this relationship over longer time periods. With sufficient precision in future satellite retrievals, ΩHCHO observations could be useful for evaluating the adequacy of surface air quality monitoring strategies.

Investigating the Relationship between Air Pollutants and Meteorological Parameters Using Satellite Data over Bangladesh

Understanding of the relationship between air pollutants and meteorological parameters on the regional scale is a prerequisite for setting up air pollution prevention and control strategies; however, there is a lack of methodical investigations, particularly in the context of Bangladesh’s deficiency of information on air pollution. This study represents the first attempt to investigate the relationship between air pollutants (NO2, O3, SO2, and CO) and meteorological parameters over Bangladesh using satellite data (OMI and MOPITT) during the period from 2015 to 2020. Geographically weighted regression (GWR) modelling was utilized to assess the relationship between air pollutants and weather variables. The spatial representation and average values of geographically varying coefficients showed that the column densities of air pollutants were affected by the meteorological parameters. For example, NO2 was positively associated with temperature in most of the studied regions, with an average geographically varying coefficient value of 0.12 Dobson units (DU, 1 DU = 2.687 × 1016 molecules/cm2), indicating that NO2 concentrations increase by 0.12 DU/year with every unit increase in temperature. The sources of NO2 and SO2 in Dhaka were identified through emission inventory analysis, and transportation and industry emissions were the most significant influencing factors for NO2 and SO2, respectively. Temperature and pressure showed a higher degree of relationship with all four air pollutants compared with other parameters. The results and discussion presented in this study can be of benefit for policy makers in developing air pollution control strategies in Bangladesh.

Rossby Waves in Total Ozone over the Arctic in 2000–2021

The purpose of this work is to study Rossby wave parameters in total ozone over the Arctic in 2000–2021. We consider the averages in the January–March period, when stratospheric trace gases (including ozone) in sudden stratospheric warming events are strongly disturbed by planetary waves. To characterize the wave parameters, we analyzed ozone data at the latitudes of 50°N (the sub-vortex area), 60°N (the polar vortex edge) and 70°N (inner region of the polar vortex). Total ozone column (TOC) measurements over a 22-year time interval were used from the Total Ozone Mapping Spectrometer/Earth Probe and Ozone Mapping Instrument/Aura satellite observations. The TOC zonal distribution and variations in the Fourier spectral components with zonal wave numbers m = 1–5 are presented. The daily and interannual variations in TOC, amplitudes and phases of the spectral wave components, as well as linear trends in the amplitudes of the dominant quasi-stationary wave 1 (QSW1), are discussed. The positive TOC peaks inside the vortex in 2010 and 2018 alternate with negative ones in 2011 and 2020. The extremely low TOC at 70°N in 2020 corresponds to severe depletion of stratospheric ozone over the Arctic in strong vortex conditions due to anomalously low planetary wave activity and a high positive phase of the Arctic Oscillation. Interannual TOC variations in the sub-vortex region at 50°N are accompanied by a negative trend of −4.8 Dobson Units per decade in the QSW1 amplitude, statistically significant at 90% confidence level, while the trend is statistically insignificant in the vortex edge region and inside the vortex due to the increased variability in TOC and QSW1. The processes associated with quasi-circumpolar migration and quasi-stationary oscillation of the wave-1 phase depending on the polar vortex strength in 2020 and 2021 are discussed.

Spatiotemporal inhomogeneity of total column NO2 in a polluted urban area inferred from TROPOMI and Pandora intercomparisons

ABSTRACT The spatiotemporal inhomogeneity of the total column NO2 amounts (TCN) in the Seoul Metropolitan Area (SMA), Korea, was quantitatively assessed through year-round (October 2019–May 2021) TROPOMI and ground-based Pandora measurements. The average TCN over the SMA was comparable to that of major Chinese megacities, being consistently high (> 0.8 DU; Dobson Unit) during the daytime (10–17 local standard time). The autocorrelation scores of the Pandora-measured TCNs demonstrated high temporal variability attributed to the spatial inhomogeneity of NO2 emissions within the SMA and near-surface advection. Accordingly, the adequate temporal collocation range for Pandora measurements for the intercomparison with the satellite sensors was considered to be ± 5 min to avoid significant uncertainty from the temporal variability (RMSE < 0.1 DU, R2 > 0.96). TROPOMI showed better agreement with conventionally collocated Pandora measurements (0.73 < R2 < 0.76, 26–29% negative bias) than the other two satellite sensors (OMI and OMPS) attributed to its highest spatial resolution. The application of the wind-based collocation revealed that the TROPOMI showed a greater negative bias on the upwind side, which was less affected by anthropogenic emissions from the urban area, than the downwind side, and the increasing distance of the TROPOMI pixel from Pandora was the most critical factor deteriorating the intercomparison scores. The FRESCO-S TROPOMI cloud algorithm update to FRESCO-wide yielded a general increase in TROPOMI TCN, especially in the partially cloudy pixels, leaving only 11% (downwind) and 29% (upwind) negative bias from coincident Pandora measurements. Furthermore, the wind-based collocation method revealed the spatial distribution pattern of NOX (NO + NO2) emissions in the SMA, with significant emission sources in the northeastern and southeastern sides of the ground-based Pandora site in Seoul.