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Earth system models (ESMs) participating in the latest Coupled Model Intercomparison Project Phase 6 (CMIP6) simulate various components of fine particulate matter (PM2.5) as major climate forcers. Yet the model performance for PM2.5 components remains little evaluated due in part to lack of observational data. Here, we evaluate near-surface concentrations of PM2.5 and its five main components over China as simulated by fourteen CMIP6 models, including organic carbon (OC, available in 14 models), black carbon (BC, 14 models), sulfate (14 models), nitrate (4 models), and ammonium (5 models). For this purpose, we collect observational data between 2000 and 2014 from a satellite-based dataset for total PM2.5 and from 2469 measurement records in the literature for PM2.5 components. Seven models output total PM2.5 concentrations, and they all underestimate the observed total PM2.5 over eastern China, with GFDL-ESM4 (–1.5 %) and MPI-ESM-1-2-HAM (–1.1 %) exhibiting the smallest biases averaged over the whole country. The other seven models, for which we recalculate total PM2.5 from the available components output, underestimate the total PM2.5 concentrations, partly because of the missing model representations of nitrate and ammonium. Concentrations of the five individual components are underestimated in almost all models, except that sulfate is overestimated in MPI-ESM-1-2-HAM by 12.6 % and in MRI-ESM2-0 by 24.5 %. The underestimation is the largest for OC (by –71.2 % to –37.8 % across the 14 models) and the smallest for BC (–47.9 % to –12.1 %). The multi-model mean (MMM) reproduces fairly well the observed spatial pattern for OC (R = 0.51), sulfate (R = 0.57), nitrate (R = 0.70) and ammonium (R = 0.75), yet the agreement is poorer for BC (R = 0.39). The varying performances of ESMs on total PM2.5 and its components have important implications for the modeled magnitude and spatial pattern of aerosol radiative forcing. [ABSTRACT FROM AUTHOR]

Nitrogen dioxide (NO2) is a major air pollutant. Tropospheric NO2 vertical column densities (VCDs) retrieved from sun-synchronous satellite instruments have provided abundant NO2 data for environmental studies, but such data are limited by insufficient temporal sampling (e.g., once a day). The Geostationary Environment Monitoring Spectrometer (GEMS) launched in February 2020 monitors NO2 at an unprecedented high temporal resolution. Here we present a research product for tropospheric NO2 VCDs, referred to as POMINO-GEMS. We develop a hybrid retrieval method combining GEMS and TROPOMI observations as well as GEOS-Chem simulations to generate hourly tropospheric NO2 slant column densities (SCDs). We then derive tropospheric NO2 air mass factors (AMFs) with explicit corrections for the anisotropy of surface reflectance and aerosol optical effects, through pixel-by-pixel radiative transfer calculations. Prerequisite cloud parameters are retrieved with the O2-O2 algorithm by using ancillary parameters consistent with those used in NO2 AMF calculations. Initial retrieval of POMINO-GEMS tropospheric NO2 VCDs for June-August 2021 reveals strong hotspot signals over megacities and distinctive diurnal variations over polluted and clean areas. POMINO-GEMS NO2 VCDs agree well with our POMINO-TROPOMI v1.2.2 product (R = 0.97, and NMB = 3.6%) over Asia. Comparison with ground-based MAX-DOAS VCD data at nine sites shows a small bias of POMINO-GEMS (NMB = -15.7%); however, the correlation for diurnal variation varies from -0.66 to 0.90, suggesting location-dependent performance. Surface NO2 concentrations estimated from POMINO-GEMS VCDs are consistent with measurements from the Ministry of Ecology and Environment of China at 855 sites (NMB = -24.1%, and R = 0.95 for diurnal correlation averaged over all sites). POMINO-GEMS data will be made freely available for users to study the spatiotemporal variations, sources and impacts of NO2. [ABSTRACT FROM AUTHOR]

We present a new product with explicit aerosol corrections, POMINO-TROPOMI, for tropospheric nitrogen dioxide (NO2) vertical column densities (VCDs) over East Asia, based on the newly launched TROPOspheric Monitoring Instrument with an unprecedented high horizontal resolution. Compared to the official TM5-MP-DOMINO (OFFLINE) product, POMINO-TROPOMI shows stronger concentration gradients near emission source locations and better agrees with MAX-DOAS measurements (R² = 0.75, NMB = 0.8 % versus R² = 0.68, NMB = 41.9 %). Sensitivity tests suggest that implicit aerosol corrections, as in TM5-MP-DOMINO, lead to underestimations of NO2 columns by about 25 % over the polluted Northern East China region. Reducing the horizontal resolution of a priori NO2 profiles would underestimate the retrieved NO2 columns over isolated city clusters in western China by 35 % but with overestimates by more than 50 % over many offshore coastal areas. The effect of a priori NO2 profiles is more important under calm conditions. [ABSTRACT FROM AUTHOR]

Satellite retrieval of vertical column densities (VCDs) of tropospheric nitrogen dioxide (NO2) is critical for NOx pollution and impact evaluation. For regions with high aerosol loadings, the retrieval accuracy is greatly affected by whether aerosol optical effects are treated implicitly (as additional "effective" clouds) or explicitly, among other factors. Our previous POMINO algorithm explicitly accounts for aerosol effects to improve the retrieval especially in polluted situations over China, by using aerosol information from GEOS-Chem simulations with further monthly constraint by MODIS/Aqua AOD data. This study updates the retrieval algorithm to POMINO v1.1, by constructing a monthly climatological dataset of aerosol extinction profiles, based on Level-2 CALIOP/CALIPSO data over 2007-2015, to better constrain the modeled aerosol profiles. We find that GEOS-Chem captures the month-to-month variation of CALIOP aerosol layer height but with a systematic underestimate by about 300-600 m (season and location dependent), due to a too strong vertical gradient of extinction above 1 km. Correcting the model aerosol extinction profiles results in small changes in retrieved cloud fraction, increases in cloud top pressure (within 2-6 % in most cases), and increases in tropospheric NO2 VCD by 4-16 % over China on a monthly basis in 2012. The improved NO2 VCDs (in POMINO v1.1) are more consistent with independent ground-based MAX-DOAS observations (R² = 0.80, NMB = -3.4 %) than POMINO (R² = 0.80, NMB = -9.6 %) and DOMINO v2 (R² = 0.68, NMB = -2.1 %) are. Especially on haze days, R² reaches 0.76 for POMINO v1.1, much higher than that for POMINO (0.68) and DOMINO v2 (0.38). Furthermore, the increase in cloud pressure likely reveals a more realistic vertical relationship between cloud and aerosol layers, with aerosols situated above the clouds in certain months instead of always below the clouds. Our POMINO v1.1 algorithm will be applied to the recently launched TropOMI sensor. [ABSTRACT FROM AUTHOR]

Horizontal visibility measured at ground meteorological stations provides an under-exploited source of information for studying the interdecadal variation of aerosols and their climatic impacts. Here we propose to use a 3-hourly visibility dataset to infer aerosol optical depth (AOD) over East China, using the nested GEOS-Chem chemical transport model to interpret the spatiotemporally varying relations between columnar and near-surface aerosols. Our analysis is focused in 2006 under cloud-free conditions. We evaluate the visibility-inferred AOD using MODIS/Terra and MODIS/Aqua AOD datasets, after validating MODIS data against three ground AOD measurement networks (AERONET, CARSNET and CSHNET). We find that the two MODIS datasets agree with ground-based AOD measurements, with negative mean biases of 0.05-0.08 and Reduced Major Axis regression slopes around unity. Visibility-inferred AOD roughly capture the general spatiotemporal patterns of the two MODIS datasets with negligible mean differences. The inferred AOD reproduce the seasonal variability (correlation exceeds 0.9) and the slight AOD growth from the late morning to early afternoon shown in the MODIS datasets, suggesting the validity of our AOD inference method. Future research will extend the visibility-based AOD inference to study the long-term variability of AOD. [ABSTRACT FROM AUTHOR]

A new type of Eu(III) ofloxacin complex as the fluorescent pH indicator has been presented. Compared to pure ligand, the complex offers more distinguished color changes (green-red-blue) derived from both lanthanide line emissions and the secondary ionization steps of ofloxacin. During the concentration dependence experiments, the photoluminescence studies on the complex showed that the excitation of this pH probe can occur at a very long wavelength which extends to visible range (Ex = 427 nm). Furthermore, the functional complex was successfully incorporated into soft networks and two novel luminescent hydrogels (rod and film) were fabricated. The soft materials also exhibited specific responses towards the pH variation. Finally, the onion cell-stain experiments were carried out to further confirm the validity of pH dependence and the results support the idea that the material will be suitable for monitoring biological samples in the future. [ABSTRACT FROM AUTHOR]

China is the world's largest emitter of anthropogenic air pollutants, and measurable amounts of Chinese pollution are transported via the atmosphere to other countries, including the United States. However, a large fraction of Chinese emissions is due to manufacture of goods for foreign consumption. Here, we analyze the impacts of trade-related Chinese air pollutant emissions on the global atmospheric environment, linking an economic-emission analysis and atmospheric chemical transport modeling. We find that in 2006, 36% of anthropogenic sulfur dioxide, 27% of nitrogen oxides, 22% of carbon monoxide, and 17% of black carbon emitted in China were associated with production of goods for export. For each of these pollutants, about 21% of export-related Chinese emissions were attributed to China-to-US export. Atmospheric modeling shows that transport of the export-related Chinese pollution contributed 3-10% of annual mean surface sulfate concentrations and 0.5-1.5% of ozone over the western United States in 2006. This Chinese pollution also resulted in one extra day or more of noncompliance with the US ozone standard in 2006 over the Los Angeles area and many regions in the eastern United States. On a daily basis, the export-related Chinese pollution contributed, at a maximum, 12-24% of sulfate concentrations over the western United States. As the United States outsourced manufacturing to China, sulfate pollution in 2006 increased in the western United States but decreased in the eastern United States, reflecting the competing effect between enhanced transport of Chinese pollution and reduced US emissions. Our findings are relevant to international efforts to reduce transboundary air pollution. [ABSTRACT FROM AUTHOR]

The Chinese government has moved aggressively since 2005 to reduce emissions of a number of pollutants including primary particulate matter (PM) and sulfur dioxide (SO2), efforts inadvertently aided since late 2008 by economic recession. Satellite observations of aerosol optical depth (AOD) and column nitrogen dioxide (NO2) provide independent indicators of emission trends, clearly reflecting the sharp onset of the recession in the fall of 2008 and rebound of the economy in the latter half of 2009. Comparison of AOD with ground-based observations of PM over a longer period indicate that emission-control policies have not been successful in reducing concentrations of aerosol pollutants at smaller size range over industrialized regions of China. The lack of success is attributed to the increasing importance of anthropogenic secondary aerosols formed from precursor species including nitrogen oxides (NOx), non-methane volatile organic compounds (NMVOC) and ammonia (NH3). [ABSTRACT FROM AUTHOR]

The GEOS-Chem model has been updated with the SAPRC-11 aromatics chemical mechanism, with the purpose of evaluating global and regional effects of the most abundant aromatics (benzene, toluene, xylenes) on the chemical species important for tropospheric oxidation capacity. The model evaluation based on surface and aircraft observations indicates good agreement for aromatics and ozone. A comparison between scenarios in GEOS-Chem with simplified aromatic chemistry (as in the standard setup, with no ozone formation from related peroxy radicals or recycling of NOx) and with the SAPRC-11 scheme reveals relatively slight changes in ozone, hydroxyl radical, and nitrogen oxides on a global mean basis (1-4%), although remarkable regional differences (5-20%) exist near the source regions. NOx decreases over the source regions and increases in the remote troposphere, due mainly to more efficient transport of peroxyacetyl nitrate (PAN), which is increased with the SAPRC aromatic chemistry. Model ozone mixing ratios with the updated aromatic chemistry increase by up to 5ppb (more than 10%), especially in industrially polluted regions. The ozone change is partly due to the direct influence of aromatic oxidation products on ozone production rates, and in part to the altered spatial distribution of NOx that enhances the tropospheric ozone production efficiency. Improved representation of aromatics is important to simulate the tropospheric oxidation. [ABSTRACT FROM AUTHOR]

Modeling atmospheric chemistry at fine resolution globally is computationally expensive; the capability to focus on specific geographic regions using a multiscale grid is desirable. Here, we develop, validate, and demonstrate stretched-grids in the GEOS-Chem atmospheric chemistry model in its high performance implementation (GCHP). These multiscale grids are specified at runtime by four parameters that offer users nimble control of the region that is refined and the resolution of the refinement. We validate the stretched-grid simulation versus global cubed-sphere simulations. We demonstrate the operation and flexibility of stretched-grid simulations with two case studies that compare simulated tropospheric NO2 column densities from stretched-grid and cubed-sphere simulations to retrieved column densities from the TROPOspheric Monitoring Instrument (TROPOMI). The first case study uses a stretched-grid with a broad refinement covering the contiguous US to produce simulated columns that perform similarly to a C180 (~50 km) cubed-sphere simulation at less than one-ninth the computational expense. The second case study experiments with a large stretch-factor for a global stretched-grid simulation with a highly localized refinement with ~10 km resolution for California. We find that the refinement improves spatial agreement with TROPOMI columns compared to a C90 cubed-sphere simulation of comparable computational demands, despite conducting the simulation at a finer resolution than parent meteorological fields. Overall we find that stretched-grids in GEOS-Chem are a practical tool for fine resolution regional- or continental-scale simulations of atmospheric chemistry. Stretched-grids are available in GEOS-Chem version 13.0.0. [ABSTRACT FROM AUTHOR]

The article discusses a study which described the use of satellite observations and information to track the dynamics of carbon dioxide emissions during COVID-19 pandemic in China. TROPOspheric Monitoring Instrument onboard the Copernicus Sentinel-5 Precursor satellite was employed to observe nitrogen dioxide. Results of the study are discussed. Materials and methods used are described.

The article cities a research study that examines carbon dioxide emissions in various Chinese cities and government's efforts on city-level climate change mitigation. It is said that policy-makers need increasingly specific information about the sources of carbon dioxide in order to reduce emissions.

China emits a considerable amount of air pollutants when producing goods for export. Previous efforts have emphasized the magnitude of export-related emissions; however, their health consequences on the Chinese population have not been quantified. Here, we present an interdisciplinary study to estimate the health impact of export-related air pollution. The results show that export-related emissions elevated the annual mean population weighted PM2.5 by 8.3 μg/m³ (15% of the total) in 2007, causing 157,000 deaths and accounting for 12% of the total mortality attributable to PM2.5-related air pollution. Compared to the eastern coastal provinces, the inner regions experience much larger export-related health losses relative to their economic production gains, owing to huge inter-regional disparities in export structures and technology levels. A shift away from emission-intensive production structure and export patterns, especially in inner regions, could significantly help improve national exports while alleviating the inter-regional cost-benefit inequality. Our results provide the first quantification of health consequences from air pollution related to Chinese exports. The proposed policy recommendations, based on health burden, economic production gains, and emission analysis, would be helpful to develop more sustainable and effective national and regional export strategies. [ABSTRACT FROM AUTHOR]