Kengo Sudo 교수

Abstract. We present an overview of state-of-the-art chemistry–climate and chemistry transport models that are used within phase 1 of the Chemistry–Climate Model Initiative (CCMI-1). The CCMI aims to conduct a detailed evaluation of participating models using process-oriented diagnostics derived from observations in order to gain confidence in the models' projections of the stratospheric ozone layer, tropospheric composition, air quality, where applicable global climate change, and the interacti

Abstract. Global surface emissions of nitrogen oxides (NOx) over a 10-year period (2005–2014) are estimated from an assimilation of multiple satellite data sets: tropospheric NO2 columns from Ozone Monitoring Instrument (OMI), Global Ozone Monitoring Experiment-2 (GOME-2), and Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY), O3 profiles from Tropospheric Emission Spectrometer (TES), CO profiles from Measurement of Pollution in the Troposphere (MOPITT), and O3 an

We present a new global three‐dimensional chemical model for the troposphere, named chemical atmospheric general circulation model (AGCM) for study of atmospheric environment and radiative forcing (CHASER). This model, developed in the framework of the Center for Climate System Research/National Institute for Environment Studies (CCSR/NIES) AGCM, is aimed to study tropospheric photochemistry and its influences on climate. The chemical component of the model simulates the O 3 ‐HO x ‐NO x ‐CH 4 ‐C

We examine contributions from various source regions to global distributions and budgets of tropospheric ozone (O 3 ) in the context of intercontinental transport, using tagged tracer simulation with a global chemical transport model. For tagging O 3 , we consider regional separation of the model domain on the basis of the distributions of O 3 chemical production. We define 14 polluted source regions (14 tracers) in the boundary layer (North America, Europe, China, etc.) and 8 regions (8 tracers

Abstract. An assessment of global particulate nitrate and ammonium aerosol based on simulations from nine models participating in the Aerosol Comparisons between Observations and Models (AeroCom) phase III study is presented. A budget analysis was conducted to understand the typical magnitude, distribution, and diversity of the aerosols and their precursors among the models. To gain confidence regarding model performance, the model results were evaluated with various observations globally, inclu

Abstract. This study presents the results from the Tropospheric Chemistry Reanalysis version 2 (TCR-2) for the period 2005–2018 at 1.1∘ horizontal resolution obtained from the assimilation of multiple updated satellite measurements of ozone, CO, NO2, HNO3, and SO2 from the OMI, SCIAMACHY, GOME-2, TES, MLS, and MOPITT satellite instruments. The reanalysis calculation was conducted using a global chemical transport model MIROC-CHASER and an ensemble Kalman filter technique that optimizes both chem

Ambient air pollution from ground-level ozone and fine particulate matter (PM_2.5) 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 PM_2.5 at sele

We assess future climate change impacts on stratosphere‐troposphere exchange (STE) and their influences on tropospheric O 3 , using a chemistry coupled climate model. Tropospheric O 3 distribution and budget were predicted decadally for 1990 to 2100 with emission changes (for O 3 precursors) and climate change specified by the IPCC SRES‐A2 scenario. Our simulations show increases in stratospheric O 3 transport to the troposphere as a result of enhancement in the tropospheric and stratospheric ci

Abstract. We conducted long-term network observations using standardized Multi-Axis Differential optical absorption spectroscopy (MAX-DOAS) instruments in Russia and ASia (MADRAS) from 2007 onwards and made the first synthetic data analysis. At seven locations (Cape Hedo, Fukue and Yokosuka in Japan, Hefei in China, Gwangju in Korea, and Tomsk and Zvenigorod in Russia) with different levels of pollution, we obtained 80 927 retrievals of tropospheric NO2 vertical column density (TropoNO2VCD) and

Abstract. This study uses multi-model ensemble results of 11 models from the second phase of Task Force Hemispheric Transport of Air Pollution (HTAP II) to calculate the global sulfur (S) and nitrogen (N) deposition in 2010. Modeled wet deposition is evaluated with observation networks in North America, Europe and East Asia. The modeled results agree well with observations, with 76–83 % of stations being predicted within ±50 % of observations. The models underestimate SO42-, NO3- and NH4+ wet de

We present results from a global three‐dimensional chemical model for the troposphere, named Chemical AGCM for Study of Atmospheric Environment and Radiative Forcing (CHASER). This model has been developed to simulate the tropospheric photochemistry involving the O 3 ‐HO x ‐NO x ‐CH 4 ‐CO photochemical system and oxidation of nonmethane hydrocarbons (NMHCs), based on an atmospheric general circulation model (AGCM). In this paper, we present results from a climatological run of the model, and eva

Ambient air pollution from ozone and fine particulate matter is associated with premature mortality. As emissions from one continent influence air quality over others, changes in emissions can also influence human health on other continents. We estimate global air pollution-related premature mortality from exposure to PM_2.5 and ozone, and the avoided deaths from 20% anthropogenic emission reductions from six source regions, North America (NAM), Europe (EUR), South Asia (SAS), East Asi

Abstract. Ozone fields simulated for the first phase of the Chemistry-Climate Model Initiative (CCMI-1) will be used as forcing data in the 6th Coupled Model Intercomparison Project. Here we assess, using reference and sensitivity simulations produced for CCMI-1, the suitability of CCMI-1 model results for this process, investigating the degree of consistency amongst models regarding their responses to variations in individual forcings. We consider the influences of methane, nitrous oxide, a com

The impact of the 1997–1998 El Niño event on the tropospheric ozone distribution and related processes is assessed by a simulation using a global chemical model. The changes in tropospheric ozone observed during the 1997–1998 El Niño are considered to have been caused by large‐scale processes due to the shift in the tropical convection pattern associated with sea surface temperature (SST) changes and by large emissions of ozone precursors due to pronounced biomass burning in the Indonesian regio

Abstract. We use simultaneous observations of tropospheric ozone and outgoing longwave radiation (OLR) sensitivity to tropospheric ozone from the Tropospheric Emission Spectrometer (TES) to evaluate model tropospheric ozone and its effect on OLR simulated by a suite of chemistry-climate models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The ensemble mean of ACCMIP models show a persistent but modest tropospheric ozone low bias (5–20 ppb) in