Multi-angle Imaging SpectroRadiometer Research Articles

Distribution and transport characteristics of dust aerosol over Tibetan Plateau and Taklimakan Desert in China using MERRA-2 and CALIPSO data

Abstract The distribution and transportation characteristics of dust aerosol over the Tibetan Plateau (TP) and Taklimakan Desert (TD) were analyzed during 1980–2017 using MERRA-2 (second Modern-Era Retrospective analysis for Research and Applications) and CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) products. The aerosol optical depth (AOD) of MERRA-2 were compared with those of AERONET (Aerosol Robotic Network) at six sites and the corresponding MISR (Multi-angle Imaging SpectroRadiometer) data. The correlation coefficients were 0.73–0.88 and 0.94, respectively. The yearly AOD over the IGP (Indo-Gangetic Plain) and the TD showed a significant increasing trend. The variations of seasonal AOD and dust AOD (DAOD) over the research region were similar, showing the values decreasing from north to south and the higher values appearing in spring and summer. The DAOD/AOD ratio exceeded 0.5 during March–August and throughout whole year in the north part of the TP and the TD, respectively. The duration, strength and area of the high DAOD region over the TD have enhanced during the past 38 years. From the CALIPSO observation, it showed the dust moving from the TD to the TP was mainly through the Qaidam Basin in the layer of 4–8 km aloft and could transport as south as 30°N, with the maximum lifting height in spring. In winter, the dust over TP was mainly from the Qaidam Basin due to the suppression effect of the inversion layer over the TD. The largest profile of dust extinction coefficient appeared in spring over the TD, while in summer over the TP. The distribution and annual regional averages of base, top and thickness of dust layer were calculated and presented. It shows a long-standing dust layer of about 1 km appearing over the TP with the maximum in spring.

Characteristics of Spatial and Temporal Evolution and Investigation of Air Pollution in Guangdong-Hong Kong-Macao Greater Bay Area Based on Ground-Space Observation Data

The temporal and spatial distribution characteristics, evolution trend and potential climatic effects of air pollution in the Guangdong-Hong Kong-Macao Greater Bay Area (GBA) were analyzed on different time scales and spatial spaces, based on ground environment observation data from June 2014 to December 2018 and satellite remote sensing inversion products from 2000 to 2018. The results show that:① From the in-situ observed daily average concentration of PM2.5, good or mild to moderate pollution occurred in January, February, October, November, and December every year, and the rest of the time was excellent. ② Based on the annual average PM2.5 concentration obtained by satellite for the past 20 years, the spatial characteristics showed that the external radiation is centered on Guangzhou and Foshan. The time evolution shows the characteristics of an Ω shape, which increases gradually from 2000 to 2009, is highest in 2008, and then gradually decreases. ③ The monthly average aerosol optical thickness (AOT) value from the Multi-angle Imaging Spectro Radiometer satellite reversion every 10 years for a period (2000-2009 for a period, 2010-2018 for a period) was used to see the monthly variation. The monthly average AOT value in the first period was larger than that in the second period of the same month, the maximum value was in March and April, and the minimum value was in November and December. It is envisaged to draw a line along the north-south direction of the Pearl River Port, which basically shows that the AOT value in the west is greater than that in the east. ④ According to the observed daily average concentration data of O3-8h, the main concentration level of O3-8h in the GBA is excellent. The cities with good ozone concentration were most numerous in 2014, with five cities, and least in 2018, with only one city. The highest ozone concentration was in September, followed by June and November, and then May and July. In the past 20 years, the spatial distribution of the average concentration of O3 monitored by satellite remote sensing showed a characteristic Ω shape, increasing initially and then decreasing. The maximum value was in May, and the north-south boundary line appeared in space. ⑤ There is a good linear relationship between the interannual variation of monthly mean temperature and radiation, whereas the relationship between AOT and radiation cannot be described by a simple linear relationship.

The 2018 fire season in North America as seen by TROPOMI: aerosol layer height intercomparisons and evaluation of model-derived plume heights

Abstract. Before the launch of the TROPOspheric Monitoring Instrument (TROPOMI), only two other satellite instruments were able to observe aerosol plume heights globally, the Multi-angle Imaging SpectroRadiometer (MISR) and Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP). The TROPOMI aerosol layer height is a potential game changer, since it has daily global coverage, and the aerosol layer height retrieval is available in near real time. The aerosol layer height can be useful for aviation and air quality alerts, as well as for improving air quality forecasting related to wildfires. Here, TROPOMI's aerosol layer height product is evaluated with MISR and CALIOP observations for wildfire plumes in North America for the 2018 fire season (June to August). Further, observing system simulation experiments were performed to interpret the fundamental differences between the different products. The results show that MISR and TROPOMI are, in theory, very close for aerosol profiles with single plumes. For more complex profiles with multiple plumes, however, different plume heights are retrieved; the MISR plume height represents the top layer, and the plume height retrieved with TROPOMI tends to have an average altitude of several plume layers. The comparison between TROPOMI and MISR plume heights shows that, on average, the TROPOMI aerosol layer heights are lower, by approximately 600 m, compared to MISR, which is likely due to the different measurement techniques. From the comparison to CALIOP, our results show that the TROPOMI aerosol layer height is more accurate over dark surfaces, for thicker plumes, and plumes between approximately 1 and 4.5 km. MISR and TROPOMI are further used to evaluate the plume height of Environment and Climate Change Canada's operational forecasting system FireWork with fire plume injection height estimates from the Canadian Forest Fire Emissions Prediction System (CFFEPS). The modelled plume heights are similar compared to the satellite observations but tend to be slightly higher with average differences of 270–580 and 60–320 m compared to TROPOMI and MISR, respectively.

An Effective and Efficient Enhanced Fixed Rank Smoothing Method for the Spatiotemporal Fusion of Multiple-Satellite Aerosol Optical Depth Products

Current reported spatiotemporal solutions for fusing multisensor aerosol optical depth (AOD) products used to recover gaps either suffer from unacceptable accuracy levels, i.e., fixed rank smooth (FRS), or high time costs, i.e., Bayesian maximum entropy (BME). This problem is generally more serious when dealing with multiple AOD products in a long time series or over large geographic areas. This study proposes a new, effective, and efficient enhanced FRS method (FRS-EE) to fuse satellite AOD products with uncertainty constraints. AOD products used in the fusion experiment include Moderate Resolution Imaging SpectroRadiometer (MODIS) DB/DT_DB_Combined AOD and Multiangle Imaging SpectroRadiometer (MISR) AOD across mainland China from 2016 to 2017. Results show that the average completeness of original, initial FRS fused, and FRS-EE fused AODs with uncertainty constraints are 22.80%, 95.18%, and 65.84%, respectively. Although the correlation coefficient (R = 0.77), root mean square error (RMSE = 0.30), and mean bias (Bias = 0.023) of the initial FRS fused AODs are relatively lower than those of original AODs compared to Aerosol Robotic Network (AERONET) AOD records, the accuracy of FRS-EE fused AODs, which are R = 0.88, RMSE = 0.20, and Bias = 0.022, is obviously improved. More importantly, in regions with fully missing original AODs, the accuracy of FRS-EE fused AODs is close to that of original AODs in regions with valid retrievals. Meanwhile, the time cost of FRS-EE for AOD fusion was only 2.91 h; obviously lower than the 30.46 months taken for BME.

Satellite-Derived PM2.5 Composition and Its Differential Effect on Children’s Lung Function

Studies of the association between air pollution and children’s health typically rely on fixed-site monitors to determine exposures, which have spatial and temporal limitations. Satellite observations of aerosols provide the coverage that fixed-site monitors lack, enabling more refined exposure assessments. Using aerosol optical depth (AOD) data from the Multiangle Imaging SpectroRadiometer (MISR) instrument, we predicted fine particulate matter, PM 2.5 , and PM 2.5 speciation concentrations and linked them to the residential locations of 1206 children enrolled in the Southern California Children’s Health Study. We fitted mixed-effects models to examine the relationship between the MISR-derived exposure estimates and lung function, measured as forced expiratory volume in 1 second (FEV 1 ) and forced vital capacity (FVC), adjusting for study community and biological factors. Gradient Boosting and Support Vector Machines showed excellent predictive performance for PM 2.5 (test R 2 = 0.68 ) and its chemical components (test R 2 = –0.71). In single-pollutant models, FEV 1 decreased by 131 mL (95% CI: − 232 , − 35 ) per 10.7-µg/m 3 increase in PM 2.5 , by 158 mL (95% CI: − 273 , − 43 ) per 1.2-µg/m 3 in sulfates (SO 4 2 − ), and by 177 mL (95% CI: − 306 , − 56 ) per 1.6-µg/m 3 increase in dust; FVC decreased by 175 mL (95% CI: − 310 , − 29 ) per 1.2-µg/m 3 increase in SO 4 2 − and by 212 mL (95% CI: − 391 , − 28 ) per 2.5-µg/m 3 increase in nitrates (NO 3 − ). These results demonstrate that satellite observations can strengthen epidemiological studies investigating air pollution health effects by providing spatially and temporally resolved exposure estimates.

Replacing missing values in the standard Multi-angle Imaging SpectroRadiometer (MISR) radiometric camera-by-camera cloud mask (RCCM) data product

Abstract. The Multi-angle Imaging SpectroRadiometer (MISR) is one of the five instruments hosted on board the NASA Terra platform, launched on 18 December 1999. This instrument has been operational since 24 February 2000 and is still acquiring Earth observation data as of this writing. The primary mission of the MISR is to document the state and properties of the atmosphere, in particular the clouds and aerosols it contains, as well as the planetary surface, on the basis of 36 data channels collectively gathered by its nine cameras (pointing in different directions along the orbital track) in four spectral bands (blue, green, red and near-infrared). The radiometric camera-by-camera cloud mask (RCCM) is derived from the calibrated measurements at the nominal top of the atmosphere and is provided separately for each of the nine cameras. This RCCM data product is permanently archived at the NASA Atmospheric Science Data Center (ASDC) in Hampton, VA, USA, and is openly accessible (Diner et al., 1999b, and https://doi.org/10.5067/Terra/MISR/MIRCCM_L2.004). For various technical reasons described in this paper, this RCCM product exhibits missing data, even though an estimate of the clear or cloudy status of the environment at each individual observed location can be deduced from the available measurements. The aims of this paper are (1) to describe how to replace over 99 % of the missing values by estimates and (2) to briefly describe the software to replace missing RCCM values, which is openly available to the community from the GitHub website, https://github.com/mmverstraete/MISR\\ RCCM/ (last access: 12 March 2020), or https://doi.org/10.5281/ZENODO.3240017 (Verstraete, 2019e). Two additional sets of resources are also made available on the research data repository of GFZ Data Services in conjunction with this paper. The first set (A; Verstraete et al., 2020; https://doi.org/10.5880/fidgeo.2020.004) includes three items: (A1) a compressed archive, RCCM_Out.zip, containing all intermediary, final and ancillary outputs created while generating the figures of this paper; (A2) a user manual, RCCM_Out.pdf, describing how to install, uncompress and explore those files; and (A3) a separate input MISR data archive, RCCM_input_68050.zip, for Path 168, Orbit 68050. This latter archive is usable with (B), the second set (Verstraete and Vogt, 2020; https://doi.org/10.5880/fidgeo.2020.008), which includes (B1), a stand-alone, self-contained, executable version of the RCCM correction codes, RCCM_Soft_Win.zip, using the IDL Virtual Machine technology that does not require a paid IDL license, as well as (B2), a user manual, RCCM_Soft_Win.pdf, to explain how to install, uncompress and use this software.

Beijing Climate Center Earth System Model version 1 (BCC-ESM1): model description and evaluation of aerosol simulations

Abstract. The Beijing Climate Center Earth System Model version 1 (BCC-ESM1) is the first version of a fully coupled Earth system model with interactive atmospheric chemistry and aerosols developed by the Beijing Climate Center, China Meteorological Administration. Major aerosol species (including sulfate, organic carbon, black carbon, dust, and sea salt) and greenhouse gases are interactively simulated with a whole panoply of processes controlling emission, transport, gas-phase chemical reactions, secondary aerosol formation, gravitational settling, dry deposition, and wet scavenging by clouds and precipitation. Effects of aerosols on radiation, cloud, and precipitation are fully treated. The performance of BCC-ESM1 in simulating aerosols and their optical properties is comprehensively evaluated as required by the Aerosol Chemistry Model Intercomparison Project (AerChemMIP), covering the preindustrial mean state and time evolution from 1850 to 2014. The simulated aerosols from BCC-ESM1 are quite coherent with Coupled Model Intercomparison Project Phase 5 (CMIP5)-recommended data, in situ measurements from surface networks (such as IMPROVE in the US and EMEP in Europe), and aircraft observations. A comparison of modeled aerosol optical depth (AOD) at 550 nm with satellite observations retrieved from the Moderate Resolution Imaging Spectroradiometer (MODIS) and the Multi-angle Imaging SpectroRadiometer (MISR) and surface AOD observations from the AErosol RObotic NETwork (AERONET) shows reasonable agreement between simulated and observed AOD. However, BCC-ESM1 shows weaker upward transport of aerosols from the surface to the middle and upper troposphere, likely reflecting the deficiency of representing deep convective transport of chemical species in BCC-ESM1. With an overall good agreement between BCC-ESM1 simulated and observed aerosol properties, it demonstrates a success of the implementation of interactive aerosol and atmospheric chemistry in BCC-ESM1.

Validation of Space-Based Albedo Products from Upscaled Tower-Based Measurements Over Heterogeneous and Homogeneous Landscapes

Surface albedo is a fundamental radiative parameter as it controls the Earth’s energy budget and directly affects the Earth’s climate. Satellite observations have long been used to capture the temporal and spatial variations of surface albedo because of their continuous global coverage. However, space-based albedo products are often affected by errors in the atmospheric correction, multi-angular bi-directional reflectance distribution function (BRDF) modelling, as well as spectral conversions. To validate space-based albedo products, an in situ tower albedometer is often used to provide continuous “ground truth” measurements of surface albedo over an extended area. Since space-based albedo and tower-measured albedo are produced at different spatial scales, they can be directly compared only for specific homogeneous land surfaces. However, most land surfaces are inherently heterogeneous with surface properties that vary over a wide range of spatial scales. In this work, tower-measured albedo products, including both directional hemispherical reflectance (DHR) and bi-hemispherical reflectance (BHR), are upscaled to coarse satellite spatial resolutions using a new method. This strategy uses high-resolution satellite derived surface albedos to fill the gaps between the albedometer’s field-of-view (FoV) and coarse satellite scales. The high-resolution surface albedo is generated from a combination of surface reflectance retrieved from high-resolution Earth Observation (HR-EO) data and moderate resolution imaging spectroradiometer (MODIS) BRDF climatology over a larger area. We implemented a recently developed atmospheric correction method, the Sensor Invariant Atmospheric Correction (SIAC), to retrieve surface reflectance from HR-EO (e.g., Sentinel-2 and Landsat-8) top-of-atmosphere (TOA) reflectance measurements. This SIAC processing provides an estimated uncertainty for the retrieved surface spectral reflectance at the HR-EO pixel level and shows excellent agreement with the standard Landsat 8 Surface Reflectance Code (LaSRC) in retrieving Landsat-8 surface reflectance. Atmospheric correction of Sentinel-2 data is vastly improved by SIAC when compared against the use of in situ AErosol RObotic NETwork (AERONET) data. Based on this, we can trace the uncertainty of tower-measured albedo during its propagation through high-resolution EO measurements up to coarse satellite scales. These upscaled albedo products can then be compared with space-based albedo products over heterogeneous land surfaces. In this study, both tower-measured albedo and upscaled albedo products are examined at Ground Based Observation for Validation (GbOV) stations (https://land.copernicus.eu/global/gbov/), and used to compare with satellite observations, including Copernicus Global Land Service (CGLS) based on ProbaV and VEGETATION 2 data, MODIS and multi-angle imaging spectroradiometer (MISR).

Random forest models for PM2.5 speciation concentrations using MISR fractional AODs

It is increasingly recognized that various chemical components of PM2.5 might have differential toxicities to human health, although such studies are hindered by the sparse or non-existent coverage of ground PM2.5 speciation monitors. The Multi-angle Imaging SpectroRadiometer (MISR) onboard the Terra satellite has an innovative design to provide information about aerosol shape, size and extinction that are more related to PM2.5 speciation concentrations. In this study, we developed random forest models that incorporated ground measurements of PM2.5 species, MISR fractional AODs, simulated PM2.5 speciation concentrations from a chemical transport model (CTM), land use variables and meteorological fields, to predict ground-level daily PM2.5 sulfate, nitrate, organic carbon (OC) and elemental carbon (EC) concentrations in California between 2005 and 2014. Our models had out-of-bag R2 of 0.72, 0.70, 0.68 and 0.70 for sulfate, nitrate, OC and EC, respectively. We also conducted sensitivity tests to explore the influence of variable selection on model performance. Results show that if there are sufficient ground measurements and predictor data to support the most sophisticated model structure, fractional AODs and total AOD have similar predicting power in estimating PM2.5 species. Otherwise, models using fractional AODs outperform those with total AOD. PM2.5 speciation concentrations are more sensitive to land use variables than other supporting data (e.g., CTM simulations and meteorological information).

Wildfire Smoke Particle Properties and Evolution, from Space-Based Multi-Angle Imaging

Emitted smoke composition is determined by properties of the biomass burning source and ambient ecosystem. However, conditions that mediate the partitioning of black carbon (BC) and brown carbon (BrC) formation, as well as the spatial and temporal factors that drive particle evolution, are not understood adequately for many climate and air-quality related modeling applications. In situ observations provide considerable detail about aerosol microphysical and chemical properties, although sampling is extremely limited. Satellites offer the frequent global coverage that would allow for statistical characterization of emitted and evolved smoke, but generally lack microphysical detail. However, once properly validated, data from the National Aeronautics and Space Administration (NASA) Earth Observing System’s Multi-Angle Imaging Spectroradiometer (MISR) instrument can create at least a partial picture of smoke particle properties and plume evolution. We use in situ data from the Department of Energy’s Biomass Burning Observation Project (BBOP) field campaign to assess the strengths and limitations of smoke particle retrieval results from the MISR Research Aerosol (RA) retrieval algorithm. We then use MISR to characterize wildfire smoke particle properties and to identify the relevant aging factors in several cases, to the extent possible. The RA successfully maps qualitative changes in effective particle size, light absorption, and its spectral dependence, when compared to in situ observations. By observing the entire plume uniformly, the satellite data can be interpreted in terms of smoke plume evolution, including size-selective deposition, new-particle formation, and locations within the plume where BC or BrC dominates.

Spatiotemporal Characteristics of the Association between AOD and PM over the California Central Valley

Many air pollution health effects studies rely on exposure estimates of particulate matter (PM) concentrations derived from remote sensing observations of aerosol optical depth (AOD). Simple but robust calibration models between AOD and PM are therefore important for generating reliable PM exposures. We conduct an in-depth examination of the spatial and temporal characteristics of the AOD-PM2.5 relationship by leveraging data from the Distributed Regional Aerosol Gridded Observation Networks (DRAGON) field campaign where eight NASA Aerosol Robotic Network (AERONET) sites were co-located with EPA Air Quality System (AQS) monitoring sites in California’s Central Valley from November 2012 to April 2013. With this spatiotemporally rich data we found that linear calibration models (R2 = 0.35, RMSE = 10.38 μg/m3) were significantly improved when spatial (R2 = 0.45, RMSE = 9.54 μg/m3), temporal (R2 = 0.62, RMSE = 8.30 μg/m3), and spatiotemporal (R2 = 0.65, RMSE = 7.58 μg/m3) functions were included. As a use-case we applied the best spatiotemporal model to convert space-borne MultiAngle Imaging Spectroradiometer (MISR) AOD observations to predict PM2.5 over the region (R2 = 0.60, RMSE = 8.42 μg/m3). Our results imply that simple AERONET AOD-PM2.5 calibrations are robust and can be reliably applied to space-borne AOD observations, resulting in PM2.5 prediction surfaces for use in downstream applications.

Introducing the 4.4 km spatial resolution Multi-Angle Imaging SpectroRadiometer (MISR) aerosol product

Abstract. The Multi-angle Imaging SpectroRadiometer (MISR) instrument has been operational on the National Aeronautics and Space Administration (NASA) Earth Observing System (EOS) Terra satellite since early 2000, creating an extensive data set of global Earth observations. Here we introduce the latest version of the MISR aerosol products. The level 2 (swath) product, which is reported on a 4.4 km spatial grid, is designated as version 23 (V23) and contains retrieved aerosol optical depth (AOD) and aerosol particle property information derived from MISR's multi-angle observations over both land and water. The changes from the previous version of the algorithm (V22) have significant impacts on the data product and its interpretation. The V23 data set is created from two separate retrieval algorithms that are applied over dark water and land surfaces, respectively. Besides increasing the horizontal resolution to 4.4 km compared with the coarser 17.6 m resolution in V22 and streamlining the format and content, the V23 product has added geolocation information, pixel-level uncertainty estimates, and improved cloud screening. MISR data can be obtained from the NASA Langley Research Center Atmospheric Science Data Center at https://eosweb.larc.nasa.gov/project/misr/misr_table (last access: 11 October 2019). The version number for the V23 level 2 aerosol product is F13_0023. The level 3 (gridded) aerosol product is still reported at 0.5∘×0.5∘ spatial resolution with results aggregated from the higher-resolution level 2 data. The format and content at level 3 have also been updated to reflect the changes made at level 2. The level 3 product associated with the V23 level 2 product version is designated as F15_0032. Both the level 2 and level 3 products are now provided in NetCDF format.

Reversal of Aerosol Properties in Eastern China with Rapid Decline of Anthropogenic Emissions

The clean air actions of the Chinese government since 2013 have led to rapid reduction in anthropogenic emissions during the last five years. In this study, we present a regional-scale insight into the transition of aerosol properties during this special period based on integrated Moderate Resolution Imaging Spectroradiometer (MODIS), Multi-angle Imaging Spectroradiometer (MISR), and ground-based AERONET (AErosol RObotic NETwork) observations. As a response, aerosols in eastern China have exhibited notable reversal in both the amount and optical properties. Regional haze pollution with Aerosol Optical Depth (AOD) > 1.0 in northern China declined from more than ~80 days per year to less than ~30 days. While fine-mode particles exhibited a continuous decrease by ~30-40% during the time period of 2013–2018, the levels of coarse aerosols had no regular variations. MISR fraction AOD of different size modes shows that there has been an obvious overall decline in coarse particles over eastern China, but natural sources such as long-range dust transport make a considerable contribution. The Single Scattering Albedo (SSA) increased steadily from 2001 to 2012 by more than ~0.05. In contrast, aerosol absorption has been getting stronger since 2013, with SSA increasing by ~0.03, due to a much larger reduction in sulfate and nitrate. The drastic transition of aerosol properties has greatly changed aerosol radiative forcing (ARF) in eastern China. The negative ARF at the top (TOA) and bottom (BOA) of the atmosphere decreased by ~30 and ~50 W/m2, respectively, in Beijing during the 2001–2012 period. Although aerosol loading continued to decline after 2013, the magnitudes of TOA and BOA ARF have increased by ~10 and ~30 W/m2, respectively, since 2013, due largely to the enhanced aerosol absorption. Our results suggest that more comprehensive observations are needed to improve understanding of the intense climate and environment effects of dramatic aerosol properties in eastern China.

The potential of satellite FPAR product for GPP estimation: An indirect evaluation using solar-induced chlorophyll fluorescence

Satellite remotely sensed fraction of photosynthetically active radiation (FPAR) products are widely used in land-surface monitoring and modeling, especially for estimating global terrestrial photosynthetic activity through light use efficiency (LUE) models. PAR absorbed by active chlorophyll (APARchl) is directly linked to vegetation photosynthesis and can be used to estimate ecosystem gross primary production (GPP). Previous studies have demonstrated that solar induced chlorophyll fluorescence has very tight relationship with APARchl at various ecosystems. Therefore, the solar angle normalized SIF (nSIF) is directly related to the fraction of PAR absorbed by chlorophyll (FPARchl). This paper intercompared six space FPAR products from Moderate Resolution Imaging Spectroradiometer (MODIS), Visible Infrared Imaging Radiometer Suite (VIIRS), Copernicus Global Land Service (CGLS), Multi-angle Imaging SpectroRadiometer (MISR), Earth Polychromatic Imaging Camera (EPIC) and Ocean and Land Colour Instrument (OLCI). Their potential relationships with FPARchl were indirectly evaluated with both spaceborne (Orbiting Carbon Observatory-2, OCO-2 and TROPOspheric Monitoring Instrument, TROPOMI) and airborne (Chlorophyll Fluorescence Imaging Spectrometer, CFIS) nSIF data as well as in situ GPP measurements. Our results show that these FPAR products are different in terms of amplitudes and seasonal variations across biomes. Among six FPAR products, OLCI FPAR shows the best relationships with TROPOMI nSIF740, OCO-2 nSIF757, and CFIS nSIF755. The coefficient of determination (R2) for the relationship between OLCI FPAR and TROPOMI nSIF740 is 0.79 ± 0.17 on a global average. APAR calculated from OLCI also exhibits the best relationship (R2 = 0.79) with in situ GPP over 25 flux towers.

Six global biomass burning emission datasets: intercomparison and application in one global aerosol model

Abstract. Aerosols from biomass burning (BB) emissions are poorly constrained in global and regional models, resulting in a high level of uncertainty in understanding their impacts. In this study, we compared six BB aerosol emission datasets for 2008 globally as well as in 14 regions. The six BB emission datasets are (1) GFED3.1 (Global Fire Emissions Database version 3.1), (2) GFED4s (GFED version 4 with small fires), (3) FINN1.5 (FIre INventory from NCAR version 1.5), (4) GFAS1.2 (Global Fire Assimilation System version 1.2), (5) FEER1.0 (Fire Energetics and Emissions Research version 1.0), and (6) QFED2.4 (Quick Fire Emissions Dataset version 2.4). The global total emission amounts from these six BB emission datasets differed by a factor of 3.8, ranging from 13.76 to 51.93 Tg for organic carbon and from 1.65 to 5.54 Tg for black carbon. In most of the regions, QFED2.4 and FEER1.0, which are based on satellite observations of fire radiative power (FRP) and constrained by aerosol optical depth (AOD) data from the Moderate Resolution Imaging Spectroradiometer (MODIS), yielded higher BB aerosol emissions than the rest by a factor of 2–4. By comparison, the BB aerosol emissions estimated from GFED4s and GFED3.1, which are based on satellite burned-area data, without AOD constraints, were at the low end of the range. In order to examine the sensitivity of model-simulated AOD to the different BB emission datasets, we ingested these six BB emission datasets separately into the same global model, the NASA Goddard Earth Observing System (GEOS) model, and compared the simulated AOD with observed AOD from the AErosol RObotic NETwork (AERONET) and the Multiangle Imaging SpectroRadiometer (MISR) in the 14 regions during 2008. In Southern Hemisphere Africa (SHAF) and South America (SHSA), where aerosols tend to be clearly dominated by smoke in September, the simulated AOD values were underestimated in almost all experiments compared to MISR, except for the QFED2.4 run in SHSA. The model-simulated AOD values based on FEER1.0 and QFED2.4 were the closest to the corresponding AERONET data, being, respectively, about 73 % and 100 % of the AERONET observed AOD at Alta Floresta in SHSA and about 49 % and 46 % at Mongu in SHAF. The simulated AOD based on the other four BB emission datasets accounted for only ∼50 % of the AERONET AOD at Alta Floresta and ∼20 % at Mongu. Overall, during the biomass burning peak seasons, at most of the selected AERONET sites in each region, the AOD values simulated with QFED2.4 were the highest and closest to AERONET and MISR observations, followed closely by FEER1.0. However, the QFED2.4 run tends to overestimate AOD in the region of SHSA, and the QFED2.4 BB emission dataset is tuned with the GEOS model. In contrast, the FEER1.0 BB emission dataset is derived in a more model-independent fashion and is more physically based since its emission coefficients are independently derived at each grid box. Therefore, we recommend the FEER1.0 BB emission dataset for aerosol-focused hindcast experiments in the two biomass-burning-dominated regions in the Southern Hemisphere, SHAF, and SHSA (as well as in other regions but with lower confidence). The differences between these six BB emission datasets are attributable to the approaches and input data used to derive BB emissions, such as whether AOD from satellite observations is used as a constraint, whether the approaches to parameterize the fire activities are based on burned area, FRP, or active fire count, and which set of emission factors is chosen.

Pollution Trends in China from 2000 to 2017: A Multi-Sensor View from Space

Satellite sensors can provide unique views of global pollution information from space. In particular, a series of aerosol and trace gas monitoring instruments have been operating for more than a decade, providing the opportunity to analyze temporal trends of major pollutants on a large scale. In this study, we integrate aerosol products from MODIS (MODIS Resolution Imaging Spectroradiometer, all abbreviations and their definitions are listed alphabetically in Abbreviations) and MISR (Multi-angle Imaging Spectroradiometer), the AAI (Absorbing Aerosol Index) product from OMI (Ozone Monitoring Instrument), column SO2 and NO2 concentrations from OMI, and tropospheric column ozone concentration from OMI/MLS (Microwave Limb Sounder) to study temporal changes in major pollutants over China. MODIS and MISR consistently revealed that column AOD (Aerosol Optical Depth) increased from 2000, peaked around 2007, and started to decline afterward, except for northwest and northeast China, where a continuous upward trend was found. Extensive negative trends in both SO2 and NO2 have also been found over major pollution source regions since ~2005. On the other hand, the OMI AAI exhibited significant increases over north China, especially the northeast and northwest regions. These places also have a decreased Angstrom exponent as revealed by MISR, indicating an increased fraction of large particles. In general, summer had the largest AOD, SO2, and NO2 trends, whereas AAI trends were strongest for autumn and winter. A multi-regression analysis showed that much of the AOD variance over major pollution source regions could be explained by SO2, NO2, and AAI combined, and that the SO2 and NO2 reduction was likely to be responsible for the negative AOD trends, while the AOD increase over NE and NW China may be associated with an increase of coarse particles revealed by increased AAI and decreased AE. In contrast to aerosols, tropospheric ozone exhibited a steady increase from 2005 throughout China. This indicates that although the recent emission control effectively reduced aerosol pollutants, ozone remains a challenging issue and may dominate future air pollution.

Interpreting the volcanological processes of Kamchatka, based on multi-sensor satellite observations

Volcanoes are complex environmental systems that pose challenges to scientific study, due to their inherently hazardous nature and in many cases, remote locations. Satellite-based remote sensing provides a useful tool for assessing both ongoing activity and retrospective eruptions. This paper represents an initial application of a multi-sensor approach, in part to demonstrate its strengths and limitations in a single volcanic region that is fairly well monitored in situ. We utilize data from five NASA satellite-based instruments, having up to 18 years of global observations, to conduct in-depth investigations of eight volcanoes on the Kamchatka Peninsula (Russia) that were active between 2000 and 2018. From 169 eruptive plumes observed, we performed detailed plume-dynamics analysis in eighty-two cases for which sufficiently favorable observations were obtained. Plume heights from MISR and CALIOP, microphysical particle properties (e.g. fine ash, sulfates) from MISR, thermal anomalies generated by lava features from MODIS, and sulfur dioxide (SO2) concentrations from OMI and OMPS are all considered. Evidence of eruption evolution over months-to-years was identified at Shiveluch, Kliuchevskoi, Kizimen, Karymsky, Zhupanovsky, Koryaksky and Kambalny. In cases with extensive data coverage (Kliuchevskoi, Kizimen, Karymsky and Zhupanovsky), underlying subsurface dynamics is inferred, corroborated where possible with detailed ground-based data records. The 1.1 km resolution of the particle property retrievals from the Multi-angle Imaging SpectroRadiometer (MISR) instrument capture downwind plume-particle evolution in many cases. Comparison of changes in aerosol optical depth (AOD), retrieved effective particle size (REPS) and retrieved effective particle absorption (REPA) map to six plume transport regimes, indicating varying degrees of downwind particle aggregation, deposition, and/or new particle formation. Distinct meteorological conditions are identified as likely driving these evolutionary processes, most notably the atmospheric static stability and wind shear at plume altitude. This approach can be applied to volcanic plumes globally, including those for which surface monitoring is limited or entirely absent.

Evaluation of the MISR fine resolution aerosol product using MODIS, MISR, and ground observations over China

Recently, NASA's Multiangle Imaging SpectroRadiometer (MISR) team released the Version 23 (V23) 4.4-km Aerosol Optical Depth (AOD) product, which has better spatial resolution than V22 at 17.6 km. However, its quality has not been validated in China. Here, V23 products for different spatiotemporal domains are obtained for validation against Aerosol Robotic NETwork (AERONET) AOD measurements for 29 sites from 2008 to 2017. Based on the national daily mean, V23 AOD yields a correlation coefficient (R) of 0.902 with AERONET; 59.45% of retrievals fall within the expected error (=EE; ±0.05 or ±0.2×AOD). A mean error (ME) of −0.0605 with 24.11% of retrievals falling below the EE indicates that MISR data are still underestimated at high AODs. The sample numbers and accuracies of spatially averaged 17.6-km and 50-km data are greatly improved relative to V22. The seasonal mean of V23 retrievals = EE in fall and winter are highest, followed by those in summer and spring; the validation results at 17.6 km are generally better than those at 50 km. By region, V23 retrievals = EE in the Beijing–Tianjin–Hebei (BTH), Yangtze River Delta (YRD) and Pearl River Delta (PRD) regions are 68.87%, 61.43%, and 73.13% respectively, while that of Taiwan is below 60% (55.75%). No V22 records exist in PRD, and V23 products over other regions in all seasons perform well; V22 retrievals in summer are also recommended. Compared with Terra/MODIS 3-km AOD in 2016, the V23 product has a slightly higher R value (0.925) with AERONET than MODIS (0.909). The MISR AOD bias is lower, and MODIS AOD is overestimated relative to the ground truth; both present consistent seasonality characteristics (spring > winter > summer > autumn), with the maximum in March and minimum in August. To investigate the spatiotemporal characteristics over long-term AOD, MISR V23 4.4-km AOD can be used in combination with other observation data.

The sensitivity of Southern Ocean aerosols and cloud microphysics to sea spray and sulfate aerosol production in the HadGEM3-GA7.1 chemistry–climate model

Abstract. With low concentrations of tropospheric aerosol, the Southern Ocean offers a “natural laboratory” for studies of aerosol–cloud interactions. Aerosols over the Southern Ocean are produced from biogenic activity in the ocean, which generates sulfate aerosol via dimethylsulfide (DMS) oxidation, and from strong winds and waves that lead to bubble bursting and sea spray emission. Here, we evaluate the representation of Southern Ocean aerosols in the Hadley Centre Global Environmental Model version 3, Global Atmosphere 7.1 (HadGEM3-GA7.1) chemistry–climate model. Compared with aerosol optical depth (AOD) observations from two satellite instruments (the Moderate Resolution Imaging Spectroradiometer, MODIS-Aqua c6.1, and the Multi-angle Imaging Spectroradiometer, MISR), the model simulates too-high AOD during winter and too-low AOD during summer. By switching off DMS emission in the model, we show that sea spray aerosol is the dominant contributor to AOD during winter. In turn, the simulated sea spray aerosol flux depends on near-surface wind speed. By examining MODIS AOD as a function of wind speed from the ERA-Interim reanalysis and comparing it with the model, we show that the sea spray aerosol source function in HadGEM3-GA7.1 overestimates the wind speed dependency. We test a recently developed sea spray aerosol source function derived from measurements made on a Southern Ocean research voyage in 2018. In this source function, the wind speed dependency of the sea spray aerosol flux is less than in the formulation currently implemented in HadGEM3-GA7.1. The new source function leads to good agreement between simulated and observed wintertime AODs over the Southern Ocean; however, it reveals partially compensating errors in DMS-derived AOD. While previous work has tested assumptions regarding the seawater climatology or sea–air flux of DMS, we test the sensitivity of simulated AOD, cloud condensation nuclei and cloud droplet number concentration to three atmospheric sulfate chemistry schemes. The first scheme adds DMS oxidation by halogens and the other two test a recently developed sulfate chemistry scheme for the marine troposphere; one tests gas-phase chemistry only, while the second adds extra aqueous-phase sulfate reactions. We show how simulated sulfur dioxide and sulfuric acid profiles over the Southern Ocean change as a result and how the number concentration and particle size of the soluble Aitken, accumulation and coarse aerosol modes are affected. The new DMS chemistry scheme leads to a 20 % increase in the number concentration of cloud condensation nuclei and cloud droplets, which improves agreement with observations. Our results highlight the importance of atmospheric chemistry for simulating aerosols and clouds accurately over the Southern Ocean.

How should we aggregate data? Methods accounting for the numerical distributions, with an assessment of aerosol optical depth

Abstract. Many applications of geophysical data – whether from surface observations, satellite retrievals, or model simulations – rely on aggregates produced at coarser spatial (e.g. degrees) and/or temporal (e.g. daily and monthly) resolution than the highest available from the technique. Almost all of these aggregates report the arithmetic mean and standard deviation as summary statistics, which are what data users employ in their analyses. These statistics are most meaningful for normally distributed data; however, for some quantities, such as aerosol optical depth (AOD), it is well-known that distributions are on large scales closer to log-normal, for which a geometric mean and standard deviation would be more appropriate. This study presents a method of assessing whether a given sample of data is more consistent with an underlying normal or log-normal distribution, using the Shapiro–Wilk test, and tests AOD frequency distributions on spatial scales of 1∘ and daily, monthly, and seasonal temporal scales. A broadly consistent picture is observed using Aerosol Robotic Network (AERONET), Multiangle Imaging SpectroRadiometer (MISR), Moderate Resolution Imagining Spectroradiometer (MODIS), and Goddard Earth Observing System Version 5 Nature Run (G5NR) data. These data sets are complementary: AERONET has the highest AOD accuracy but is sparse, and MISR and MODIS represent different satellite retrieval techniques and sampling. As a model simulation, G5NR is spatiotemporally complete. As timescales increase from days to months to seasons, data become increasingly more consistent with log-normal than normal distributions, and the differences between arithmetic- and geometric-mean AOD become larger, with geometric mean becoming systematically smaller. Assuming normality systematically overstates both the typical level of AOD and its variability. There is considerable regional heterogeneity in the results: in low-AOD regions such as the open ocean and mountains, often the AOD difference is small enough (<0.01) to be unimportant for many applications, especially on daily timescales. However, in continental outflow regions and near source regions over land, and on monthly or seasonal timescales, the difference is frequently larger than the Global Climate Observation System (GCOS) goal uncertainty in a climate data record (the larger of 0.03 or 10 %). This is important because it shows that the sensitivity to an averaging method can and often does introduce systematic effects larger than the total goal GCOS uncertainty. Using three well-studied AERONET sites, the magnitude of estimated AOD trends is shown to be sensitive to the choice of arithmetic vs. geometric means, although the signs are consistent. The main recommendations from the study are that (1) the distribution of a geophysical quantity should be analysed in order to assess how best to aggregate it, (2) ideally AOD aggregates such as satellite level 3 products (but also ground-based data and model simulations) should report a geometric-mean or median AOD rather than (or in addition to) arithmetic-mean AOD, and (3) as this is unlikely in the short term due to the computational burden involved, users can calculate geometric-mean monthly aggregates from widely available daily mean data as a stopgap, as daily aggregates are less sensitive to the choice of aggregation scheme than those for monthly or seasonal aggregates. Furthermore, distribution shapes can have implications for the validity of statistical metrics often used for comparison and evaluation of data sets. The methodology is not restricted to AOD and can be applied to other quantities.