GSTDTAP  > 地球科学
DOI10.5194/acp-19-10087-2019
Clear-sky ultraviolet radiation modelling using output from the Chemistry Climate Model Initiative
Lamy, Kevin1; 39;Connor, Fiona M.2
2019-08-12
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2019
卷号19期号:15页码:10087-10110
文章类型Article
语种英语
国家France; South Africa; Switzerland; New Zealand; Japan; England; Germany; Italy; USA; Canada
英文摘要

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 degrees N-30 degrees 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.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000480463900001
WOS关键词REPRESENTATIVE CONCENTRATION PATHWAYS ; ABSORPTION CROSS-SECTIONS ; OZONE RETURN DATES ; SOLAR UV-RADIATION ; STRATOSPHERIC OZONE ; SATELLITE MEASUREMENTS ; TROPOSPHERIC OZONE ; MIDDLE ATMOSPHERE ; PART 1 ; VERSION
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/185948
专题地球科学
作者单位1.Univ La Reunion, Lab Atmosphere & Cyclones, LACy, Meteo France,UMR CNRS 8105, St Denis, La Reunion, France;
2.CNRM UMR 3589, Meteo France, CNRS, Toulouse, France;
3.Univ Lille, Fac Sci & Technol, LOA, Villeneuve Dascq, France;
4.Pierre & Marie Curie Univ, Inst Pierre Simon Laplace, Serv Aeron LATMOS, Lab Atmospheres Milieux Observat Spatiales,CNRS, Paris, France;
5.Univ KwaZulu Natal, Sch Chem & Phys, Durban, South Africa;
6.ETH Zurich ETHZ, Inst Atmospher & Climate Sci, Zurich, Switzerland;
7.Bodeker Sci, Christchurch, New Zealand;
8.Univ Canterbury, Sch Phys & Chem Sci, Christchurch, New Zealand;
9.Natl Inst Environm Studies, Tsukuba, Ibaraki, Japan;
10.Univ Reading, Dept Meteorol, Reading, Berks, England;
11.Deutsch Zentrum Luft & Raumfahrt DLR, Inst Phys Atmosphare, Oberpfaffenhofen, Germany;
12.Karlsruhe Inst Technol, Steinbuch Ctr Comp, Karlsruhe, Germany;
13.Natl Inst Water & Atmospher Res NIWA, Wellington, New Zealand;
14.Univ Cambridge, Dept Chem, Cambridge, England;
15.Natl Ctr Atmospher Sci, Cambridge, England;
16.Met Off Hadley Ctr, Exeter, Devon, England;
17.Univ Leeds, Sch Earth & Environm, Leeds, W Yorkshire, England;
18.Univ Aquila, Dept Phys & Chem Sci, Laquila, Italy;
19.Meteorol Res Inst, Tsukuba, Ibaraki, Japan;
20.Natl Ctr Atmospher Res, POB 3000, Boulder, CO 80307 USA;
21.NASA, Goddard Space Flight Ctr, Greenbelt, MD USA;
22.Environm & Climate Change Canada, Montreal, PQ, Canada;
23.World Radiat Ctr, Phys Meteorol Observatorium Davos, Davos, Switzerland;
24.Nagoya Univ, Grad Sch Environm Studies, Nagoya, Aichi, Japan;
25.Cornell Univ, Sibley Sch Mech & Aerosp Engn, Ithaca, NY 14853 USA
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Lamy, Kevin,39;Connor, Fiona M.. Clear-sky ultraviolet radiation modelling using output from the Chemistry Climate Model Initiative[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2019,19(15):10087-10110.
APA Lamy, Kevin,&39;Connor, Fiona M..(2019).Clear-sky ultraviolet radiation modelling using output from the Chemistry Climate Model Initiative.ATMOSPHERIC CHEMISTRY AND PHYSICS,19(15),10087-10110.
MLA Lamy, Kevin,et al."Clear-sky ultraviolet radiation modelling using output from the Chemistry Climate Model Initiative".ATMOSPHERIC CHEMISTRY AND PHYSICS 19.15(2019):10087-10110.
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