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Featured researches published by Irene Cionni.


Journal of Climate | 2010

Chemistry-climate model simulations of twenty-first century stratospheric climate and circulation changes

Neal Butchart; Irene Cionni; Veronika Eyring; Theodore G. Shepherd; Darryn W. Waugh; Hideharu Akiyoshi; J. Austin; C. Brühl; M. P. Chipperfield; Eugene C. Cordero; Martin Dameris; Rudolf Deckert; S. Dhomse; S. M. Frith; Rolando R. Garcia; Andrew Gettelman; Marco A. Giorgetta; Douglas E. Kinnison; Feng Li; E. Mancini; Charles McLandress; Steven Pawson; G. Pitari; David A. Plummer; E. Rozanov; F. Sassi; J. F. Scinocca; K. Shibata; B. Steil; Wenshou Tian

The response of stratospheric climate and circulation to increasing amounts of greenhouse gases (GHGs) and ozone recovery in the twenty-first century is analyzed in simulations of 11 chemistry–climate models using near-identical forcings and experimental setup. In addition to an overall global cooling of the stratosphere in the simulations (0.59 6 0.07 K decade 21 at 10 hPa), ozone recovery causes a warming of the Southern Hemisphere polar lower stratosphere in summer with enhanced cooling above. The rate of warming correlates with the rate of ozone recovery projected by the models and, on average, changes from 0.8 to 0.48 K decade 21 at 100 hPa as the rate of recovery declines from the first to the second half of the century. In the winter northern polar lower stratosphere the increased radiative cooling from the growing abundance of GHGs is, in most models, balanced by adiabatic warming from stronger polar downwelling. In the Antarctic lower stratosphere the models simulate an increase in low temperature extremes required for polar stratospheric cloud (PSC) formation, but the positive trend is decreasing over the twenty-first century in all models. In the Arctic, none of the models simulates a statistically significant increase in Arctic PSCs throughout the twentyfirst century. The subtropical jets accelerate in response to climate change and the ozone recovery produces a westward acceleration of the lower-stratospheric wind over the Antarctic during summer, though this response is sensitive to the rate of recovery projected by the models. There is a strengthening of the Brewer–Dobson


Environmental Research Letters | 2013

Global premature mortality due to anthropogenic outdoor air pollution and the contribution of past climate change

Raquel A. Silva; J. Jason West; Yuqiang Zhang; Susan C. Anenberg; Jean-Francois Lamarque; Drew T. Shindell; W. J. Collins; Stig B. Dalsøren; Greg Faluvegi; Gerd Folberth; Larry W. Horowitz; Tatasuya Nagashima; Vaishali Naik; Steven T. Rumbold; Ragnhild Bieltvedt Skeie; Kengo Sudo; Toshihiko Takemura; D. Bergmann; Philip Cameron-Smith; Irene Cionni; Ruth M. Doherty; Veronika Eyring; B. Josse; Ian A. MacKenzie; David A. Plummer; Mattia Righi; David S. Stevenson; Sophie Szopa; Guang Zeng

Increased concentrations of ozone and fine particulate matter (PM2.5) since preindustrial times reflect increased emissions, but also contributions of past climate change. Here we use modeled concentrations from an ensemble of chemistry?climate models to estimate the global burden of anthropogenic outdoor air pollution on present-day premature human mortality, and the component of that burden attributable to past climate change. Using simulated concentrations for 2000 and 1850 and concentration?response functions (CRFs), we estimate that, at present, 470?000 (95% confidence interval, 140?000 to 900?000) premature respiratory deaths are associated globally and annually with anthropogenic ozone, and 2.1 (1.3 to 3.0) million deaths with anthropogenic PM2.5-related cardiopulmonary diseases (93%) and lung cancer (7%). These estimates are smaller than ones from previous studies because we use modeled 1850 air pollution rather than a counterfactual low concentration, and because of different emissions. Uncertainty in CRFs contributes more to overall uncertainty than the spread of model results. Mortality attributed to the effects of past climate change on air quality is considerably smaller than the global burden: 1500 (?20?000 to 27?000) deaths yr?1 due to ozone and 2200 (?350?000 to 140?000) due to PM2.5. The small multi-model means are coincidental, as there are larger ranges of results for individual models, reflected in the large uncertainties, with some models suggesting that past climate change has reduced air pollution mortality.


Journal of Geophysical Research | 2014

Stratospheric ozone response to sulfate geoengineering: Results from the Geoengineering Model Intercomparison Project (GeoMIP)

Giovanni Pitari; Valentina Aquila; Ben Kravitz; Alan Robock; Shingo Watanabe; Irene Cionni; Natalia De Luca; Glauco Di Genova; E. Mancini; Simone Tilmes

Geoengineering with stratospheric sulfate aerosols has been proposed as a means of temporarily cooling the planet, alleviating some of the side effects of anthropogenic CO2 emissions. However, one of the known side effects of stratospheric injections of sulfate aerosols under present-day conditions is a general decrease in ozone concentrations. Here we present the results from two general circulation models and two coupled chemistry-climate models within the experiments G3 and G4 of the Geoengineering Model Intercomparison Project. On average, the models simulate in G4 an increase in sulfate aerosol surface area density similar to conditions a year after the Mount Pinatubo eruption and a decrease in globally averaged ozone by 1.1−2.1 DU (Dobson unit, 1 DU = 0.001 atm cm) during the central decade of the experiment (2040–2049). Enhanced heterogeneous chemistry on sulfate aerosols leads to an ozone increase in low and middle latitudes, whereas enhanced heterogeneous reactions in polar regions and increased tropical upwelling lead to a reduction of stratospheric ozone. The increase in UV-B radiation at the surface due to ozone depletion is offset by the screening due to the aerosols in the tropics and midlatitudes, while in polar regions the UV-B radiation is increased by 5% on average, with 12% peak increases during springtime. The contribution of ozone changes to the tropopause radiative forcing during 2040–2049 is found to be less than −0.1 W m−2. After 2050, because of decreasing ClOx concentrations, the suppression of the NOx cycle becomes more important than destruction of ozone by ClOx, causing an increase in total stratospheric ozone.


Global Change Biology | 2016

Comparing concentration-based (AOT40) and stomatal uptake (PODY) metrics for ozone risk assessment to European forests

Alessandro Anav; A. De Marco; Chiara Proietti; Andrea Alessandri; A. Dell'Aquilla; Irene Cionni; Pierre Friedlingstein; Dmitry Khvorostyanov; Laurent Menut; Elena Paoletti; Pierre Sicard; Stephen Sitch; Marcello Vitale

Tropospheric ozone (O3) produces harmful effects to forests and crops, leading to a reduction of land carbon assimilation that, consequently, influences the land sink and the crop yield production. To assess the potential negative O3 impacts to vegetation, the European Union uses the Accumulated Ozone over Threshold of 40 ppb (AOT40). This index has been chosen for its simplicity and flexibility in handling different ecosystems as well as for its linear relationships with yield or biomass loss. However, AOT40 does not give any information on the physiological O3 uptake into the leaves since it does not include any environmental constraints to O3 uptake through stomata. Therefore, an index based on stomatal O3 uptake (i.e. PODY), which describes the amount of O3 entering into the leaves, would be more appropriate. Specifically, the PODY metric considers the effects of multiple climatic factors, vegetation characteristics and local and phenological inputs rather than the only atmospheric O3 concentration. For this reason, the use of PODY in the O3 risk assessment for vegetation is becoming recommended. We compare different potential O3 risk assessments based on two methodologies (i.e. AOT40 and stomatal O3 uptake) using a framework of mesoscale models that produces hourly meteorological and O3 data at high spatial resolution (12 km) over Europe for the time period 2000-2005. Results indicate a remarkable spatial and temporal inconsistency between the two indices, suggesting that a new definition of European legislative standard is needed in the near future. Besides, our risk assessment based on AOT40 shows a good consistency compared to both in-situ data and other model-based datasets. Conversely, risk assessment based on stomatal O3 uptake shows different spatial patterns compared to other model-based datasets. This strong inconsistency can be likely related to a different vegetation cover and its associated parameterizations.


Atmospheric Chemistry and Physics | 2016

The effect of future ambient air pollution on human premature mortality to 2100 using output from the ACCMIP model ensemble

Raquel A. Silva; J. Jason West; Jean-Francois Lamarque; Drew T. Shindell; W. J. Collins; Stig B. Dalsøren; Greg Faluvegi; Gerd Folberth; Larry W. Horowitz; Tatsuya Nagashima; Vaishali Naik; Steven T. Rumbold; Kengo Sudo; Toshihiko Takemura; D. Bergmann; Philip Cameron-Smith; Irene Cionni; Ruth M. Doherty; Veronika Eyring; B. Josse; Ian A. MacKenzie; David S. Plummer; Mattia Righi; David S. Stevenson; Sophie Szopa; Guang Zeng

Ambient air pollution from ground-level ozone and fine particulate matter (PM2.5) is associated with premature mortality. Future concentrations of these air pollutants will be driven by natural and anthropogenic emissions and by climate change. Using anthropogenic and biomass burning emissions projected in the four Representative Concentration Pathway scenarios (RCPs), the ACCMIP ensemble of chemistry-climate models simulated future concentrations of ozone and PM2.5 at selected decades between 2000 and 2100. We use output from the ACCMIP ensemble, together with projections of future population and baseline mortality rates, to quantify the human premature mortality impacts of future ambient air pollution. Future air pollution-related premature mortality in 2030, 2050 and 2100 is estimated for each scenario and for each model using a health impact function based on changes in concentrations of ozone and PM2.5 relative to 2000 and projected future population and baseline mortality rates. Additionally, the global mortality burden of ozone and PM2.5 in 2000 and each future period is estimated relative to 1850 concentrations, using present-day and future population and baseline mortality rates. The change in future ozone concentrations relative to 2000 is associated with excess global premature mortality in some scenarios/periods, particularly in RCP8.5 in 2100 (316 thousand deaths/year), likely driven by the large increase in methane emissions and by the net effect of climate change projected in this scenario, but it leads to considerable avoided premature mortality for the three other RCPs. However, the global mortality burden of ozone markedly increases from 382,000 (121,000 to 728,000) deaths/year in 2000 to between 1.09 and 2.36 million deaths/year in 2100, across RCPs, mostly due to the effect of increases in population and baseline mortality rates. PM2.5 concentrations decrease relative to 2000 in all scenarios, due to projected reductions in emissions, and are associated with avoided premature mortality, particularly in 2100: between -2.39 and -1.31 million deaths/year for the four RCPs. The global mortality burden of PM2.5 is estimated to decrease from 1.70 (1.30 to 2.10) million deaths/year in 2000 to between 0.95 and 1.55 million deaths/year in 2100 for the four RCPs, due to the combined effect of decreases in PM2.5 concentrations and changes in population and baseline mortality rates. Trends in future air pollution-related mortality vary regionally across scenarios, reflecting assumptions for economic growth and air pollution control specific to each RCP and region. Mortality estimates differ among chemistry-climate models due to differences in simulated pollutant concentrations, which is the greatest contributor to overall mortality uncertainty for most cases assessed here, supporting the use of model ensembles to characterize uncertainty. Increases in exposed population and baseline mortality rates of respiratory diseases magnify the impact on premature mortality of changes in future air pollutant concentrations and explain why the future global mortality burden of air pollution can exceed the current burden, even where air pollutant concentrations decrease.


Environmental Pollution | 2014

Future impacts of nitrogen deposition and climate change scenarios on forest crown defoliation

Alessandra De Marco; Chiara Proietti; Irene Cionni; R. Fischer; Augusto Screpanti; Marcello Vitale

Defoliation is an indicator for forest health in response to several stressors including air pollutants, and one of the most important parameters monitored in the International Cooperative Programme on Assessment and Monitoring of Air Pollution Effects on Forests (ICP Forests). The study aims to estimate crown defoliation in 2030, under three climate and one nitrogen deposition scenarios, based on evaluation of the most important factors (meteorological, nitrogen deposition and chemical soil parameters) affecting defoliation of twelve European tree species. The combination of favourable climate and nitrogen fertilization in the more adaptive species induces a generalized decrease of defoliation. On the other hand, severe climate change and drought are main causes of increase in defoliation in Quercus ilex and Fagus sylvatica, especially in Mediterranean area. Our results provide information on regional distribution of future defoliation, an important knowledge for identifying policies to counteract negative impacts of climate change and air pollution.


Water Air and Soil Pollution | 2014

Random Forests Analysis: a Useful Tool for Defining the Relative Importance of Environmental Conditions on Crown Defoliation

Marcello Vitale; Chiara Proietti; Irene Cionni; R. Fischer; Alessandra De Marco

Defoliation is one of the most important parameters monitored in the International Cooperative Programme on Assessment and Monitoring of Air Pollution Effects on Forests (ICP Forests). Defoliation is an indicator for forest health and vitality. Conventional statistical analysis shows weak or not significant correlations between tree crown defoliation and climatic conditions or air pollution parameters, because of its high variability. The study aims to evaluate the most important factors among climatic, pollutants (Nox and NHy) and stand parameters affecting crown defoliation of the main European tree species (Fagus sylvatica, Picea abies, Quercus ilex, Pinus sylvestris and Quercus petraea) through application of a new and powerful statistical classifier, the random forests analysis (RFA). RFA highlighted that tree crown defoliation was mainly related to age in P. abies, to geographic location in F. sylvatica and to air pollution predictors in Q. ilex, while it was similarly linked to meteorological and air pollution predictors in P. sylvestris and Q. petraea. In this study, RFA has proven to be, for the first time, a useful tool to discern the most important predictors affecting tree crown defoliation, and consequently, it can be used for an appropriate forest management.


Environmental Pollution | 2016

Impacts of air pollution on cultural heritage corrosion at European level: What has been achieved and what are the future scenarios

Francesca Di Turo; Chiara Proietti; Augusto Screpanti; M. Francesca Fornasier; Irene Cionni; Gabriele Favero; Alessandra De Marco

The interaction of pollutants with Cultural Heritage materials leads to artworks and materials degradation and loss, causing an unpriceless damage. This works aims to estimate the impacts of air pollution and meteorological conditions on limestone, copper and bronze and represents the European risk assessment for corrosion of Cultural Heritage materials. The measures and policies for atmospheric pollution reduction have cut off the SO2 concentration and consequently its impact on materials is drastically reduced. Indeed, in 1980 the number of UNESCO sites in danger was extremely high (94% for limestone, 54% for copper and 1% for bronze) while in 2010 these sites did not exceed the tolerable value of surface recession and corrosion. However, some problem related to air pollution persists. In particular, Random Forest Analysis (RFA), highlights PM10 as the main responsible for materials corrosion, in 2010. Two scenarios in 2030 have been tested, highlighting that the corrosion levels of limestone, copper and bronze exceed the tolerable limits only in the Balkan area and Turkey. Our results show the importance in the air quality modelling as a powerful tool for the UNESCO sites conservation.


Atmospheric Chemistry and Physics | 2012

Pre-industrial to end 21st century projections of tropospheric ozone from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

P. J. Young; A. T. Archibald; Kevin West Bowman; Jean-Francois Lamarque; Vaishali Naik; David S. Stevenson; Simone Tilmes; Apostolos Voulgarakis; Oliver Wild; D. Bergmann; Philip Cameron-Smith; Irene Cionni; W. J. Collins; Stig B. Dalsøren; Ruth M. Doherty; Veronika Eyring; G. Faluvegi; Larry W. Horowitz; B. Josse; Y. H. Lee; Ian A. MacKenzie; T. Nagashima; David A. Plummer; Mattia Righi; S. T. Rumbold; Ragnhild Bieltvedt Skeie; Drew T. Shindell; Kengo Sudo; Sophie Szopa; Guang Zeng


Geoscientific Model Development | 2012

The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): overview and description of models, simulations and climate diagnostics

Jean-Francois Lamarque; Drew T. Shindell; B. Josse; P. J. Young; Irene Cionni; Veronika Eyring; D. Bergmann; Philip Cameron-Smith; W. J. Collins; Ruth M. Doherty; Stig B. Dalsøren; G. Faluvegi; Gerd Folberth; Steven J. Ghan; Larry W. Horowitz; Y. H. Lee; Ian A. MacKenzie; Tatsuya Nagashima; Vaishali Naik; David A. Plummer; Mattia Righi; S. T. Rumbold; Michael Schulz; Ragnhild Bieltvedt Skeie; David S. Stevenson; Kengo Sudo; Sophie Szopa; Apostolos Voulgarakis; Guang Zeng

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Jean-Francois Lamarque

National Center for Atmospheric Research

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Larry W. Horowitz

National Oceanic and Atmospheric Administration

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Philip Cameron-Smith

Lawrence Livermore National Laboratory

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Sophie Szopa

Centre national de la recherche scientifique

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Mattia Righi

German Aerospace Center

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