scholarly journals Comparative Study of the Influence of Air Pollution on UVI at Maitri in Antarctica and New Delhi in India

2012 ◽  
Vol 2012 ◽  
pp. 1-5
Author(s):  
Nandita D. Ganguly

The influence of air pollution on the erythemal ultraviolet irradiance (UVI) reaching the earth's surface has been investigated at the Indian Antarctic station Maitri and compared with that at New Delhi, the capital of India, over a period of three years from 2005 to 2007. Total ozone column (TOC), surface ozone, NO2 column, middle tropospheric SO2 column, and BrO column are observed to exhibit a deceasing trend at Maitri, having a clean and pristine environment, while UVI and aerosol optical depth at 500 nm exhibit an increasing trend. This negative correlation suggests that O3, NO2, SO2, and BrO act as filters against erythemal ultraviolet irradiance reaching the earth's surface, while the aerosols, which are present in the atmosphere of Maitri, may not be either very effective in filtering out the UVI reaching the earth's surface or may not be large enough to produce measurable effects on UVI. TOC and BrO column are observed to exhibit a deceasing trend at New Delhi, having comparatively higher levels of pollution, while UVI, NO2 column, middle tropospheric SO2 column, surface ozone, and aerosol optical depth at 500 nm exhibit an increasing trend. This suggests that TOC and BrO act as filters against UVI, while NO2, surface ozone, SO2, and aerosols in the atmosphere of New Delhi may not be large enough to produce measurable effects on UVI.

2018 ◽  
Author(s):  
Kévin Lamy ◽  
Thierry Portafaix ◽  
Béatrice Josse ◽  
Colette Brogniez ◽  
Sophie Godin-Beekmann ◽  
...  

Abstract. We have derived values of the Ultraviolet Index (UVI) at solar noon from the Tropospheric Ultraviolet Model (TUV) driven by ozone, temperature and aerosol fields from the first phase of the Chemistry-Climate Model Initiative (CCMI-1). Since clouds remain one of the largest uncertainties in climate projections, we simulated only clear-sky UVI. We compared the UVI climatologies obtained from CCMI and TUV against present-day climatological values of UVI derived from satellite data (the OMI-Aura OMUVBd product) and ground-based measurements (from the NDACC network). Depending on the region, relative differences between the UVI obtained from CCMI and TUV and ground-based measurements ranged between −4 % and 11 %. We calculated the UVI evolution throughout the 21st century for the four Representative Concentration Pathways (RCPs 2.6, 4.5, 6.0 and 8.5). Compared to 1960s values, we found an average increase in UVI in 2100 (of 2–4 %) in the tropical belt (30° N–30° S). For the mid-latitudes, we observed a 1.8 to 3.4 % increase in the Southern Hemisphere for RCP 2.6, 4.5 and 6.0, and found a 2.3 % decrease in RCP 8.5. Higher UV indices are projected in the Northern Hemisphere except for RCP 8.5. At high latitudes, ozone recovery is well identified and induces a complete return of mean UVI levels to 1960 values for RCP 8.5 in the Southern Hemisphere. In the Northern Hemisphere, UVI levels in 2100 are higher by 0.5 to 5.5 % for RCP 2.6, 4.5 and 6.0 and they are lower by 7.9 % for RCP 8.5. We analysed the impacts of greenhouse gases (GHGs) and ozone-depleting substances (ODSs) on UVI from 1960 by comparing CCMI sensitivity simulations (1960–2100) with fixed GHGs or ODSs at their respective 1960 levels. As expected with ODS fixed at their 1960 levels, there is no large decrease in ozone levels and consequently no sudden increase in UVI levels. With fixed GHG, we observed a delayed return of ozone to 1960 values, the same signal is observed on UVI, and looking at the UVI difference between 2090s values and 1960s values, we found an 8 % increase in the tropical belt during the summer of each hemisphere. Finally, we show that, while in the Southern Hemisphere UVI is mainly driven by total ozone column, in the Northern Hemisphere both total ozone column and aerosol optical depth drive UVI levels, with aerosol optical depth having twice as much influence on UVI as total column does.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
S. Janjai ◽  
A. Sripradit ◽  
R. Wattan ◽  
S. Buntoung ◽  
S. Pattarapanitchai ◽  
...  

This paper presents a simple semi-empirical model for estimating global photosynthetically active radiation (PAR) under all sky conditions. The model expresses PAR as a function of cloud index, aerosol optical depth, total ozone column, solar zenith angle, and air mass. The formulation of the model was based on a four-year period (2008–2011) of PAR data obtained from the measurements at four solar monitoring stations in a tropical environment of Thailand. These are Chiang Mai (18.78°N, 98.98°E), Ubon Ratchathani (15.25°N, 104.87°E), Nakhon Pathom (13.82°N, 100.04°E), and Songkhla (7.20°N, 100.60°E). The cloud index was derived from MTSAT-1R satellite, whereas the aerosol optical depth was obtained from MODIS/Terra satellite. For the total ozone column, it was retrieved from OMI/Aura satellite. The model was validated against independent data set from the four stations. It was found that hourly PAR estimated from the proposed model and that obtained from the measurements were in reasonable agreement, with the root mean square difference (RMSD) and mean bias difference (MBD) of 14.3% and −5.8%, respectively. In addition, for the case of monthly average hourly PAR, RMSD and MBD were reduced to 11.1% and −5.1%, respectively.


2005 ◽  
Vol 23 (11) ◽  
pp. 3399-3406 ◽  
Author(s):  
A. de La Casinière ◽  
V. Cachorro ◽  
I. Smolskaia ◽  
J. Lenoble ◽  
M. Sorribas ◽  
...  

Abstract. A one week field campaign took place in September 2002 at El Arenosillo, Spain. The objective was to compare total ozone column (TOC) and aerosol optical depth (AOD) from near ultraviolet to near infrared, measured by several Spanish and French instruments. Three spectroradiometers, Brewer, SPUV02, and LICOR, and a CIMEL photometer, have been used simultaneously and the results are presented for four clear days. TOC values are given by the Brewer instrument, and by SPUV02, using two different methods. The ground instruments compare satisfactorily (within 5 DU) and the values are consistent with TOMS data (within 10 DU). AOD from the various instruments are compared at seven different wavelengths between 320 nm and 1020 nm: the agreement is very good at 350, 380, and 870 nm; at the four other wavelengths the difference is smaller than 0.03, which can be explained by a relative difference of 4% only between the calibrations of the various instruments. Larger AOD diurnal variations were observed at short wavelengths than in the visible and near infrared; this is most likely due to changes in aerosol size along the day, during the campaign.


2014 ◽  
Vol 14 (11) ◽  
pp. 16529-16589
Author(s):  
V. De Bock ◽  
H. De Backer ◽  
R. Van Malderen ◽  
A. Mangold ◽  
A. Delcloo

Abstract. At Uccle, a long time series (1991–2013) of simultaneous measurements of erythemal ultraviolet (UV) dose, global solar radiation, total ozone column (TOC) and Aerosol Optical Depth (AOD) (at 320.1 nm) is available which allows for an extensive study of the changes in the variables over time. A change-point analysis, which determines whether there is a significant change in the mean of the time series, is applied to the monthly anomalies time series of the variables. Only for erythemal UV dose and TOC, a significant change point (without any known instrumental cause) was present in the time series around February 1998 and March 1998 respectively. The change point in TOC corresponds with results found in literature, where the change in ozone levels (around 1997) is attributed to the recovery of ozone. Linear trends were determined for the different (monthly anomalies) time series. Erythemal UV dose, global solar radiation and TOC all increase with respectively 7, 4 and 3% per decade. AOD shows an (insignificant) negative trend of −8% per decade. These trends agree with results found in literature for sites with comparable latitudes. A multiple linear regression (MLR) analysis is applied to the data in order to study the influence of global solar radiation, TOC and AOD on the erythemal UV dose. Together these parameters are able to explain 94% of the variation in erythemal UV dose. Most of the variation (56%) in erythemal UV dose is explained by global solar radiation. The regression model performs well with a slight tendency to underestimate the measured erythemal UV doses and with a Mean Absolute Bias Error (MABE) of 18%. However, in winter, negative erythemal UV dose values are modeled. Applying the MLR to the individual seasons solves this issue. The seasonal models have an adjusted R2 value higher than 0.8 and the correlation between modeled and measured erythemal UV dose values is higher than 0.9 for each season. The summer model gives the best performance, with an absolute mean error of only 6%. Again, global solar radiation is the factor that contributes the most to the variation in erythemal UV dose, so there is no doubt about the necessity to include this factor in the regression models. A large part of the influence of AOD is already represented by the global solar radiation parameter. Therefore the individual contribution of AOD to erythemal UV dose is so low. For this reason, it seems unnecessary to include AOD in the MLR analysis. Including TOC however, is justified as the adjusted R2 increases and the MABE of the model decreases compared to a model where only global solar radiation is used as explanatory variable.


2019 ◽  
Vol 19 (15) ◽  
pp. 10087-10110 ◽  
Author(s):  
Kévin Lamy ◽  
Thierry Portafaix ◽  
Béatrice Josse ◽  
Colette Brogniez ◽  
Sophie Godin-Beekmann ◽  
...  

Abstract. We have derived values of the ultraviolet index (UVI) at solar noon using the Tropospheric Ultraviolet Model (TUV) driven by ozone, temperature and aerosol fields from climate simulations of the first phase of the Chemistry-Climate Model Initiative (CCMI-1). Since clouds remain one of the largest uncertainties in climate projections, we simulated only the clear-sky UVI. We compared the modelled UVI climatologies against present-day climatological values of UVI derived from both satellite data (the OMI-Aura OMUVBd product) and ground-based measurements (from the NDACC network). Depending on the region, relative differences between the UVI obtained from CCMI/TUV calculations and the ground-based measurements ranged between −5.9 % and 10.6 %. We then calculated the UVI evolution throughout the 21st century for the four Representative Concentration Pathways (RCPs 2.6, 4.5, 6.0 and 8.5). Compared to 1960s values, we found an average increase in the UVI in 2100 (of 2 %–4 %) in the tropical belt (30∘ N–30∘ S). For the mid-latitudes, we observed a 1.8 % to 3.4 % increase in the Southern Hemisphere for RCPs 2.6, 4.5 and 6.0 and found a 2.3 % decrease in RCP 8.5. Higher increases in UVI are projected in the Northern Hemisphere except for RCP 8.5. At high latitudes, ozone recovery is well identified and induces a complete return of mean UVI levels to 1960 values for RCP 8.5 in the Southern Hemisphere. In the Northern Hemisphere, UVI levels in 2100 are higher by 0.5 % to 5.5 % for RCPs 2.6, 4.5 and 6.0 and they are lower by 7.9 % for RCP 8.5. We analysed the impacts of greenhouse gases (GHGs) and ozone-depleting substances (ODSs) on UVI from 1960 by comparing CCMI sensitivity simulations (1960–2100) with fixed GHGs or ODSs at their respective 1960 levels. As expected with ODS fixed at their 1960 levels, there is no large decrease in ozone levels and consequently no sudden increase in UVI levels. With fixed GHG, we observed a delayed return of ozone to 1960 values, with a corresponding pattern of change observed on UVI, and looking at the UVI difference between 2090s values and 1960s values, we found an 8 % increase in the tropical belt during the summer of each hemisphere. Finally we show that, while in the Southern Hemisphere the UVI is mainly driven by total ozone column, in the Northern Hemisphere both total ozone column and aerosol optical depth drive UVI levels, with aerosol optical depth having twice as much influence on the UVI as total ozone column does.


2014 ◽  
Vol 955-959 ◽  
pp. 1591-1594
Author(s):  
Dan Li ◽  
Chang Kui Sun ◽  
Kun Yu ◽  
Lin Sun ◽  
Lei Du

This study compares the aerosol optical depth (AOD) from the HJ-1 CCD cameras with ground-based measurements of AEROSOL ROBOTIC NETWORK (AERONET). The results indicate that the HJ-1 CCD AOD retrievals at 550 nm have good correlations with the ground-based measurements. This validation study indicates that the HJ-1 CCD AOD retrievals can adequately characterize the AOD distributions over the dense dark vegetation region of China. This AOD product can act an important role to study air pollution.


2010 ◽  
Vol 10 (24) ◽  
pp. 12273-12283 ◽  
Author(s):  
J. Kar ◽  
M. N. Deeter ◽  
J. Fishman ◽  
Z. Liu ◽  
A. Omar ◽  
...  

Abstract. A large wintertime increase in pollutants has been observed over the eastern parts of the Indo Gangetic Plains. We use improved version 4 carbon monoxide (CO) retrievals from the Measurements of Pollution in the Troposphere (MOPITT) along with latest version 3 aerosol data from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) lidar instrument and the tropospheric ozone residual products to characterize this pollution pool. The feature is seen primarily in the lower troposphere from about November to February with strong concomitant increases in CO and aerosol optical depth (AOD). The signature of the feature is also observed in tropospheric ozone column data. The height resolved aerosol data from CALIPSO confirm the trapping of the pollution pool at the lowest altitudes. The observations indicate that MOPITT can capture this low altitude phenomenon even in winter conditions as indicated by the averaging kernels.


2012 ◽  
Vol 12 (5) ◽  
pp. 2469-2477 ◽  
Author(s):  
C. S. Zerefos ◽  
K. Tourpali ◽  
K. Eleftheratos ◽  
S. Kazadzis ◽  
C. Meleti ◽  
...  

Abstract. This study examines the long-term variability of UV solar irradiances at 305 nm and 325 nm over selected sites in Canada, Europe and Japan. Site selection was restricted to the availability of the most complete UV spectroradiometric datasets during the period 1990–2011. The analysis includes the long-term variability of total ozone, aerosol optical depth and cloud fraction at the sites studied. The results, based on observations and modeling, suggest that over Canada, Europe and Japan the period under study can be divided into three sub-periods of scientific merit: the first period (1991–1994) is the period perturbed by the Pinatubo volcanic eruption, during which excess volcanic aerosol has enhanced the "conventional" amplification factor of UV-B at ground level by an additional factor that depends on solar elevation. The increase of the UV-B amplification factor is the result of enhanced scattering processes caused by the injection of huge amounts of volcanic aerosols during the perturbed period. The second period (1995–2006) is characterized by a 0.14% yr−1 increase in total ozone and an increasing trend in spectral irradiance by 0.94% yr−1 at 305 nm and 0.88% yr−1 at 325 nm. That paradox was caused by the significant decline of the aerosol optical depth by more than 1% yr−1 (the "brightening" effect) and the absence of any statistically significant trend in the cloud fraction. The third period (2007–2011) shows statistically significant evidence of a slowdown or even a turning point in the previously reported upward UV-B trends over Canada, Europe and Japan.


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