scholarly journals Global distribution and 14-year changes in erythemal irradiance, UV atmospheric transmission, and total column ozone for2005–2018 estimated from OMI and EPIC observations

2020 ◽  
Vol 20 (14) ◽  
pp. 8351-8380
Author(s):  
Jay Herman ◽  
Alexander Cede ◽  
Liang Huang ◽  
Jerald Ziemke ◽  
Omar Torres ◽  
...  

Abstract. Satellite data from the Ozone Measuring Instrument (OMI) and Earth Polychromatic Imaging Camera (EPIC) are used to study long-term changes and global distribution of UV erythemal irradiance E(ζ,φ,z,t) (mW m−2) and the dimensionless UV index E ∕ (25 m Wm−2) over major cities as a function of latitude ζ, longitude φ, altitude z, and time t. Extremely high amounts of erythemal irradiance (12 < UV index <18) are found for many low-latitude and high-altitude sites (e.g., San Pedro, Chile, 2.45 km; La Paz, Bolivia, 3.78 km). Lower UV indices at some equatorial or high-altitude sites (e.g., Quito, Ecuador) occur because of persistent cloud effects. High UVI levels (UVI > 6) are also found at most mid-latitude sites during the summer months for clear-sky days. OMI time-series data starting in January 2005 to December 2018 are used to estimate 14-year changes in erythemal irradiance ΔE, total column ozone ΔTCO3, cloud and haze transmission ΔCT derived from scene reflectivity LER, and reduced transmission from absorbing aerosols ΔCA derived from absorbing aerosol optical depth τA for 191 specific cities in the Northern Hemisphere and Southern Hemisphere from 60∘ S to 60∘ N using publicly available OMI data. A list of the sites showing changes at the 1 standard deviation level 1σ is provided. For many specific sites there has been little or no change in E(ζ,φ,z,t) for the period 2005–2018. When the sites are averaged over 15∘ of latitude, there are strong correlation effects of both short- and long-term cloud and absorbing aerosol change as well as anticorrelation with total column ozone change ΔTCO3. Estimates of changes in atmospheric transmission ΔCT (ζ, φ, z, t) derived from OMI-measured cloud and haze reflectivity LER and averaged over 15∘ of latitude show an increase of 1.1±1.2 % per decade between 60 and 45∘ S, almost no average 14-year change of 0.03±0.5 % per decade from 55∘ S to 30∘ N, local increases and decreases from 20 to 30∘ N, and an increase of 1±0.9 % per decade from 35 to 60∘ N. The largest changes in E(ζ,φ,z,t) are driven by changes in cloud transmission CT. Synoptic EPIC radiance data from the sunlit Earth are used to derive ozone and reflectivity needed for global images of the distribution of E(ζ,φ,z,t) from sunrise to sunset centered on the Americas, Europe–Africa, and Asia. EPIC data are used to show the latitudinal distribution of E(ζ,φ,z,t) from the Equator to 75∘ for specific longitudes. EPIC UV erythemal images show the dominating effect of solar zenith angle (SZA), the strong increase in E with altitude, and the decreases caused by cloud cover. The nearly cloud-free images of E(ζ,φ,z,t) over Australia during the summer (December) show regions of extremely high UVI (14–16) covering large parts of the continent. Zonal averages show a maximum of UVI = 14 in the equatorial region seasonally following latitudes where SZA = 0∘. Dangerously high amounts of erythemal irradiance (12 < UV index < 18) are found for many low-latitude and high-altitude sites. High levels of UVI are known to lead to health problems (skin cancer and eye cataracts) with extended unprotected exposure, as shown in the extensive health statistics maintained by the Australian Institute of Health and Welfare and the United States National Institute of Health National Cancer Institute.

2019 ◽  
Author(s):  
Jay Herman ◽  
Alexander Cede ◽  
Liang Huang ◽  
Jerald Ziemke ◽  
Matthew Kowalewski ◽  
...  

Abstract. Satellite data from the Ozone Measuring Instrument (OMI) and Earth Polychromatic Imaging Camera (EPIC) for ozone amount and scene reflectivity (mostly from clouds) are used to study changes and global distribution of UV erythemal irradiance in mW/m2 E(ζ,&amp;varphi;,z,t) and UV index (E/25 mWm2) over the Earth's surface as a function of latitude ζ, longitude &amp;varphi;, altitude z, and time t. OMI time series data starting in January 2005 to December 2018 are used to estimate 14-year changes in total column ozone TCO3 and scene reflectivity at 105 specific land plus 77 ocean locations in the Northern and Southern Hemispheres. Estimates of changes in atmospheric transmission T(ζ,&amp;varphi;,z,t) derived from cloud and haze reflectivity show almost no average 14-year change from 55° S to 35° N but show an increase from 40° N to 60° N. This implies increased solar insolation at high northern latitudes that suggests positive feedback for global warming. TCO3 has increased at a rate of 2 % per decade for the latitudes between 60° S to 10° N changing to a decrease of 1 % per decade between 40° N to 60° N. The result is an average decrease in E(ζ,&amp;varphi;,z,t) at a rate of 2 % per decade in the Southern Hemisphere and an increase between 40° N to 60° N. For some specific sites (latitudes from 55° S to 45° N) there has been little or no change in E(ζ,&amp;varphi;,z,t) for the period 2005–2018. Nearly half the sites show the effects of both short- and long-term cloud change as well as total column ozone change. Synoptic EPIC data from the sunlit Earth are used derive ozone and reflectivity needed for global images of the distribution of E(ζ,&amp;varphi;,z,t) from sunrise to sunset centered on the Americas, Europe-Africa, and Asia. EPIC data are used to show the latitudinal distribution of E(ζ,&amp;varphi;,z,t) from the equator to 75° for specific longitudes. Dangerously high amounts of erythemal irradiance (12 


2015 ◽  
Vol 8 (10) ◽  
pp. 4487-4505 ◽  
Author(s):  
K.-L. Chang ◽  
S. Guillas ◽  
V. E. Fioletov

Abstract. Total column ozone variations estimated using ground-based stations provide important independent source of information in addition to satellite-based estimates. This estimation has been vigorously challenged by data inhomogeneity in time and by the irregularity of the spatial distribution of stations, as well as by interruptions in observation records. Furthermore, some stations have calibration issues and thus observations may drift. In this paper we compare the spatial interpolation of ozone levels using the novel stochastic partial differential equation (SPDE) approach with the covariance-based kriging. We show how these new spatial predictions are more accurate, less uncertain and more robust. We construct long-term zonal means to investigate the robustness against the absence of measurements at some stations as well as instruments drifts. We conclude that time series analyzes can benefit from the SPDE approach compared to the covariance-based kriging when stations are missing, but the positive impact of the technique is less pronounced in the case of drifts.


2015 ◽  
Vol 8 (4) ◽  
pp. 3967-4009 ◽  
Author(s):  
K.-L. Chang ◽  
S. Guillas ◽  
V. E. Fioletov

Abstract. Total column ozone variations estimated using ground-based stations provide important independent source of information in addition to satellite-based estimates. This estimation has been vigorously challenged by data inhomogeneity in time and by the irregularity of the spatial distribution of stations, as well as by interruptions in observation records. Furthermore, some stations have calibration issues and thus observations may drift. In this paper we compare the spatial interpolation of ozone levels using the novel stochastic partial differential equation (SPDE) approach with kriging. We show how these new spatial predictions are more accurate, less uncertain and more robust. We construct long-term zonal means to investigate the robustness against the absence of measurements at some stations as well as instruments drifts. We conclude that time series analyzes can benefit from the SPDE approach compared to kriging when stations are missing, but the positive impact of the technique is less pronounced in the case of drifts.


2016 ◽  
Vol 16 (24) ◽  
pp. 15619-15627 ◽  
Author(s):  
Ulrike Langematz ◽  
Franziska Schmidt ◽  
Markus Kunze ◽  
Gregory E. Bodeker ◽  
Peter Braesicke

Abstract. The year 1980 has often been used as a benchmark for the return of Antarctic ozone to conditions assumed to be unaffected by emissions of ozone-depleting substances (ODSs), implying that anthropogenic ozone depletion in Antarctica started around 1980. Here, the extent of anthropogenically driven Antarctic ozone depletion prior to 1980 is examined using output from transient chemistry–climate model (CCM) simulations from 1960 to 2000 with prescribed changes of ozone-depleting substance concentrations in conjunction with observations. A regression model is used to attribute CCM modelled and observed changes in Antarctic total column ozone to halogen-driven chemistry prior to 1980. Wintertime Antarctic ozone is strongly affected by dynamical processes that vary in amplitude from year to year and from model to model. However, when the dynamical and chemical impacts on ozone are separated, all models consistently show a long-term, halogen-induced negative trend in Antarctic ozone from 1960 to 1980. The anthropogenically driven ozone loss from 1960 to 1980 ranges between 26.4 ± 3.4 and 49.8 ± 6.2 % of the total anthropogenic ozone depletion from 1960 to 2000. An even stronger ozone decline of 56.4 ± 6.8 % was estimated from ozone observations. This analysis of the observations and simulations from 17 CCMs clarifies that while the return of Antarctic ozone to 1980 values remains a valid milestone, achieving that milestone is not indicative of full recovery of the Antarctic ozone layer from the effects of ODSs.


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.


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.


2021 ◽  
Vol 13 (9) ◽  
pp. 4425-4436
Author(s):  
Janusz W. Krzyścin ◽  
Bonawentura Rajewska-Więch ◽  
Janusz Jarosławski

Abstract. The total column ozone (TCO3) measurements by the Dobson spectrophotometer (serial no. 84) have been carried out at Belsk station (51∘50′ N, 20∘47′ E), Poland, since 23 March 1963. In total, ∼115 000 intraday manual observations were made by 31 December 2019. These observations were performed for different combinations of double wavelength pairs in the ultraviolet range and observation types, i.e., direct sun (DS), zenith blue (ZB), and zenith cloudy (ZC) depending on weather conditions. The long-term stability of the instrument was supported by frequent (almost every 4 years) intercomparisons with the world standard spectrophotometer. Trend analyses, based on the monthly and yearly averaged TCO3, can be carried out without any additional corrections to the intraday values. To adjust these data to the Brewer spectrophotometer observations, which were also performed at Belsk, a procedure is proposed to account for less accurate Dobson observations under low solar elevation, presence of clouds, and the temperature dependence of ozone absorption. The adjusted time series shows that the Brewer–Dobson monthly averaged differences are in the range of about ±0.5 %. The intraday TCO3 database, divided into three periods (1963–1979, 1980–1999, and 2000–2019), is freely available at https://doi.org/10.1594/PANGAEA.919378 (Rajewska-Więch et al., 2020).


2017 ◽  
Author(s):  
Andrew R. D. Smedley ◽  
John S. Rimmer ◽  
Ann R. Webb

Abstract. Long-term trends of total column ozone, assessments of stratospheric ozone recovery and satellite validation are underpinned by a reliance on daily “best representative values” from Brewer spectrophotometers and other ground-based ozone instruments. In turn reporting of these daily total column ozone values to the World Ozone and Ultraviolet Data Centre has traditionally been predicated upon a binomial choice between direct sun and zenith sky observations. For mid- and high-latitude monitoring sites impacted by cloud cover we discuss the potential deficiencies of this approach in terms of its rejection of otherwise valid observations and capability to evenly sample throughout the day. A new methodology is proposed that makes full use of all valid direct sun and zenith sky observations, accounting for unevenly spaced observations and their relative uncertainty, to calculate an improved estimate of the daily mean total column ozone. It is demonstrated that this method can increase the number of contributing observations by a factor of 2.5, increases the sampled time span, and reduces the spread of the representative time by half. No effect on longer-term trends is detected, though for the sample data analysed we observe a mean increase of 2.8 DU (0.82 %) w.r.t. the traditional direct sun vs zenith sky average choice. To complement the new calculation of a best representative value of total column ozone and separate its uncertainty from the spread of observations, we also propose reporting its standard error rather than the standard deviation, together with measures of the full range of values observed.


2021 ◽  
Author(s):  
Janusz W. Krzyścin ◽  
Bonawentura Rajewska-Więch ◽  
Janusz Jarosławski

Abstract. The total column ozone (TCO3) measurements by the Dobson spectrophotometer #84 have been carried out at Belsk (51°50', 20°47'), Poland, since March 23, 1963. In total, ~115,000 intra-day manual observations have been taken up to December 31, 2019. These observations were made for various combinations of double wavelength pairs in UV range (AD, CD) and the observation category, i.e., direct Sun, zenith blue, and zenith cloudy depending on the weather conditions. The long-term stability of the instrument was supported by frequent (~almost every 4 yr.) intercomparisons with the world standard spectrophotometers. Trend analyses, based on the monthly and yearly averaged TCO3, can be carried out without any additional corrections to the intraday values. To adjust this data to the Brewer spectrophotometer observations also performed at Belsk, a procedure is proposed to account for: less accurate Dobson observations under low solar elevation, presence of clouds, and sensitivity of the ozone absorption on temperature. The adjusted time series shows that the Brewer-Dobson monthly averaged differences are in the range of about ±0.5 %. The intra-day TCO3 data base, divided into three periods (1963–1979, 1980–1999, and 2000–2019), is freely available at https://doi.pangaea.de/10.1594/PANGAEA.919378 (Rajewska-Więch et al., 2020).


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