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The Plankton, Aerosol, Cloud, ocean Ecosystem (PACE) mission will carry into space the Ocean Color Instrument (OCI), a spectrometer measuring at 5nm spectral resolution in the ultraviolet (UV) to near infrared (NIR) with additional spectral bands in the shortwave infrared (SWIR), and two multi-angle polarimeters that will overlap the OCI spectral range and spatial coverage, i. e., the Spectrometer for Planetary Exploration (SPEXone) and the Hyper-Angular Rainbow Polarimeter (HARP2). These instruments, especially when used in synergy, have great potential for improving estimates of water reflectance in the post Earth Observing System (EOS) era. Extending the top-of-atmosphere (TOA) observations to the UV, where aerosol absorption is effective, adding spectral bands in the SWIR, where even the most turbid waters are black and sensitivity to the aerosol coarse mode is higher than at shorter wavelengths, and measuring in the oxygen A-band to estimate aerosol altitude will enable greater accuracy in atmospheric correction for ocean color science. The multi-angular and polarized measurements, sensitive to aerosol properties (e.g., size distribution, index of refraction), can further help to identify or constrain the aerosol model, or to retrieve directly water reflectance. Algorithms that exploit the new capabilities are presented, and their ability to improve accuracy is discussed. They embrace a modern, adapted heritage two-step algorithm and alternative schemes (deterministic, statistical) that aim at inverting the TOA signal in a single step. These schemes, by the nature of their construction, their robustness, their generalization properties, and their ability to associate uncertainties, are expected to become the new standard in the future. A strategy for atmospheric correction is presented that ensures continuity and consistency with past and present ocean-color missions while enabling full exploitation of the new dimensions and possibilities. Despite the major improvements anticipated with the PACE instruments, gaps/issues remain to be filled/tackled. They include dealing properly with whitecaps, taking into account Earth-curvature effects, correcting for adjacency effects, accounting for the coupling between scattering and absorption, modeling accurately water reflectance, and acquiring a sufficiently representative dataset of water reflectance in the UV to SWIR. Dedicated efforts, experimental and theoretical, are in order to gather the necessary information and rectify inadequacies. Ideas and solutions are put forward to address the unresolved issues. Thanks to its design and characteristics, the PACE mission will mark the beginning of a new era of unprecedented accuracy in ocean-color radiometry from space.

Year-to-year variations in the atmospheric methane (CH4) growth rate show significant correlation with climatic drivers. The second half of 2010 and the first half of 2011 experienced the strongest La Niña since the early 1980s, when global surface networks started monitoring atmospheric CH4 mole fractions. We use these surface measurements, retrievals of column-averaged CH4 mole fractions from GOSAT, new wetland inundation estimates, and atmospheric δ13C-CH4 measurements to estimate the impact of this strong La Niña on the global atmospheric CH4 budget. By performing atmospheric inversions, we find evidence of an increase in tropical CH4 emissions of ∼6-9 TgCH4 yr-1 during this event. Stable isotope data suggest that biogenic sources are the cause of this emission increase. We find a simultaneous expansion of wetland area, driven by the excess precipitation over the Tropical continents during the La Niña. Two process-based wetland models predict increases in wetland area consistent with observationally-constrained values, but substantially smaller per-area CH4 emissions, highlighting the need for improvements in such models. Overall, tropical wetland emissions during the strong La Niña were at least by 5% larger than the long-term mean.

This paper describes a neural network cloud masking scheme from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Science coupled with Observations from a Lidar) multi-angle polarimetric measurements. The algorithm has been trained on synthetic measurements and has been applied to the processing of 1 year of PARASOL data. Comparisons of the retrieved cloud fraction with MODIS (Moderate Resolution Imaging Spectroradiometer) products show overall agreement in spatial and temporal patterns, but the PARASOL neural network (PARASOL-NN) retrieves lower cloud fractions. Comparisons with a goodness-of-fit mask from aerosol retrievals suggest that the NN cloud mask flags fewer clear pixels as cloudy than MODIS (∼ 3 % of the clear pixels versus ∼ 15 % by MODIS). On the other hand the NN classifies more pixels incorrectly as clear than MODIS (∼ 20 % by NN, versus ∼ 15 % by MODIS). Additionally, the NN and MODIS cloud mask have been applied to the aerosol retrievals from PARASOL using the Remote Sensing of Trace Gas and Aerosol Products (RemoTAP) algorithm. Validation with AERONET shows that the NN cloud mask performs comparably with MODIS in screening residual cloud contamination in retrieved aerosol properties. Our study demonstrates that cloud masking from multi-angle polarimeter (MAP) aerosol retrievals can be performed based on the MAP measurements themselves, making the retrievals independent of the availability of a cloud imager. [ABSTRACT FROM AUTHOR]

From a passive satellite remote sensing point of view, the richest set of information on aerosol properties can be obtained from instruments that measure both intensity and polarization of backscattered sunlight at multiple wavelengths and multiple viewing angles for one ground pixel. However, it is challenging to exploit this information at a global scale because complex algorithms are needed with many fit parameters (aerosol and land/ocean reflection), based on online radiative transfer models. So far, two such algorithms have demonstrated this capability at a global scale: the Generalized Retrieval of Atmosphere and Surface Properties (GRASP) algorithm and the Remote sensing of Trace gas and Aerosol Products (RemoTAP) algorithm. In this paper, we present a detailed comparison of the most recent versions of RemoTAP and GRASP. We evaluate both algorithms for synthetic observations, for real PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Science coupled with Observations from a Lidar) observations against AERONET (Aerosol Robotic Network) for common pixels, and for global PARASOL retrievals for the year 2008. For the aerosol optical depth (AOD) over land, both algorithms show a root mean square error (RMSE) of 0.10 (at 550 nm). For single scattering albedo (SSA), both algorithms show a good performance in terms of RMSE (0.04), but RemoTAP has a smaller bias (0.002) compared to GRASP (0.021). For the Ångström exponent (AE), GRASP has a smaller RMSE (0.367) than RemoTAP (0.387), mainly caused by a small overestimate of AE at low values (large particles). Over ocean both algorithms perform very well. For AOD, RemoTAP has an RMSE of 0.057 and GRASP an even smaller RMSE of 0.047. For AE, the RMSEs of RemoTAP and GRASP are 0.285 and 0.224, respectively. Based on the AERONET comparison, we conclude that both algorithms show very similar overall performance, where both algorithms have stronger and weaker points. For the global data products, we find a root mean square difference (RMSD) between RemoTAP and GRASP AOD of 0.12 and 0.038 over land and ocean, respectively. The largest differences occur over the biomass burning region in equatorial Africa. The global mean values are virtually unbiased with respect to each other. For AE the RMSD between RemoTAP and GRASP is 0.33 over land and 0.23 over ocean. For SSA, we find much better agreement over land (bias = - 0.01, RMSD = 0.043 for retrievals with AOD > 0.2) than over ocean (bias = 0.053, RMSD = 0.074). As expected, the differences increase towards low AOD, over both land and ocean. We also compared the GRASP and RemoTAP AOD and AE products against MODIS. For AOD over land, the agreement of either GRASP or RemoTAP with MODIS is worse than the agreement between the two PARASOL algorithms themselves. Over ocean, the agreement is very similar among the three products for AOD. For AE, the agreement between GRASP and RemoTAP is much better than the agreement of both products with MODIS. The agreement of the latest product versions with each other and with AERONET improved significantly compared to the previous version of the global products of GRASP and RemoTAP. The results demonstrate that the dedicated effort in algorithm development for multi-angle polarimetric (MAP) aerosol retrievals still leads to substantial improvement of the resulting aerosol products, and this is still an ongoing process. [ABSTRACT FROM AUTHOR]

The University of Maryland, Baltimore County (UMBC) Hyper-Angular Rainbow Polarimeter (HARP2) will be on board NASA's Plankton, Aerosol, Cloud, ocean Ecosystem (PACE) mission, scheduled for launch in January 2024. In this study we systematically evaluate the retrievability and uncertainty of aerosol and ocean parameters from HARP2 multi-angle polarimeter (MAP) measurements. To reduce the computational demand of MAP-based retrievals and maximize data processing throughput, we developed improved neural network (NN) forward models for spaceborne HARP2 measurements over a coupled atmosphere and ocean system within the FastMAPOL retrieval algorithm. To this end, a cascading retrieval scheme is implemented in FastMAPOL, which leverages a series of NN models of varying size, speed, and accuracy to optimize performance. Two sets of NN models are used for reflectance and polarization, respectively. A full day of global synthetic HARP2 data was generated and used to test various retrieval parameters including aerosol microphysical and optical properties, aerosol layer height, ocean surface wind speed, and ocean chlorophyll a concentration. To assess retrieval quality, pixel-wise retrieval uncertainties were derived from error propagation and evaluated against the difference between the retrieval parameters and truth based on a Monte Carlo method. We found that the fine-mode aerosol properties can be retrieved well from the HARP2 data, though the coarse-mode aerosol properties are more uncertain. Larger uncertainties are associated with a reduced number of available viewing angles, which typically occur near the scan edge of the HARP2 instrument. Results of the performance assessment demonstrate that the algorithm is a viable approach for operational application to HARP2 data after the PACE launch. [ABSTRACT FROM AUTHOR]

This paper describes a neural network cloud masking scheme from PARASOL (Polarisation and Anisotropy of Reflectances for Atmospheric Science coupled with Observations from a Lidar) Multi-Angle Polarimetric measurements. The algorithm has been trained on synthetic measurements and has been applied to the processing of one year of PARASOL data. Comparisons of the retrieved cloud fraction with MODIS (Moderate Resolution Imaging Spectroradiometer) products show overall agreement in spatial and temporal patterns but the PARASOL-NN retrieves lower cloud fractions. Comparisons with a goodness-of-fit mask from aerosol retrievals suggest that the NN cloud mask flags less clear pixels as cloudy than MODIS (∼ 3% of the clear pixels, versus ∼ 15% by MODIS). On the other hand the NN classifies more pixels incorrectly as clear than MODIS (∼ 19% by NN, versus ∼ 15% by MODIS). Additionally, the NN and MODIS cloud mask have been applied to the aerosol retrievals from PARASOL using the Remote Sensing of Trace Gas and Aerosol Products (RemoTAP) algorithm. Validation with AERONET shows that the NN cloud mask performs comparably with MODIS in screening residual cloud contamination in retrieved aerosol properties. Our study demonstrates that cloud masking from MAP aerosol retrievals can be performed based on the MAP measurements themselves, making the retrievals independent of the availability of a cloud imager. [ABSTRACT FROM AUTHOR]

We apply a Local Ensemble Transform Kalman Smoother (LETKS) in combination with the global aerosol climate model ECHAM-HAM to estimate aerosol emissions from POLDER-3/PARASOL observations for the year 2006. We assimilate Aerosol Optical Depth at 550mnm (AOD550), Ångström Exponent for 550nm and 865nm (AE550-865) and Single Scattering Albedo at 550nm (SSA550) in order to improve modeled aerosol mass, size and absorption simultaneously. The new global aerosol emissions increase to 1419 Tg·yr-1 (+28%) for dust, 1850 Tg·yr-1 (+75%) for sea salt, 215 Tg·yr-1 (+143%) for organic aerosol and 13.3 Tg·yr-1 (+75%) for black carbon, while the sulfur dioxide emissions increase to 198 Tg·yr-1 (+42%) and total deposition of sulfates to 293 Tg·yr-1 (+39%). Organic and black carbon emissions are much higher than their prior values from bottom up inventories with a stronger increase in biomass burning sources (+193% and +90%) than in anthropogenic sources (115% and 70%). The evaluation of the experiments with POLDER (assimilated) and AERONET as well as MODIS Dark Target (independent) observations shows a clear improvement compared to the ECHAM-HAM control run. Specifically based on AERONET the global mean error of AOD550 improves from -0.094 to - 0.006 while AAOD550 improves from -0.009 to -0.004 after the assimilation. A smaller improvement is observed also in AE550-865 mean absolute error (from 0.428 to 0.393), with a considerably higher improvement over isolated island sites over the ocean. The new dust emissions are closer to the ensemble median of AEROCOM I, AEROCOM III and CMIP5 as well as some of the previous assimilation studies. The new sea salt emissions get closer to the reported emissions from previous studies. Indications of a missing fraction of coarse dust and sea salt particles are discussed. The biomass burning changes (based on POLDER) can be used as alternative biomass burning scaling factors for the GFAS inventory distinctively estimated for organic carbon (2.93) and black carbon (1.90), instead of the recommended scaling of 3.4 (Kaiser et al. 2012). The estimated emissions are highly sensitive to the relative humidity due to aerosol water uptake, especially in the case of the sulfates. We found that ECHAM-HAM, like most of the GCMs that participated in AEROCOM and CMIP6, overestimated the relative humidity compared to ERA-5 and as a result the water uptake by aerosols, assuming the kappa values are not underestimated. If we use the ERA-5 relative humidity, sulfate emissions must be further increased, as modeled sulfate AOD is lowered. Specifically, over East Asia, the lower AOD can be attributed to the underestimated precipitation and the lack of simulated nitrates in the model. [ABSTRACT FROM AUTHOR]

Atmospheric aerosols and their impact on cloud properties remain the largest uncertainty in the human forcing of the climate system. By increasing the concentration of cloud droplets (Nd), aerosols reduce droplet size and increase the reflectivity of clouds (a negative radiative forcing). Central to this climate impact is the susceptibility of cloud droplet number to aerosol (ß), the diversity of which explains much of the variation in radiative forcing in global climate models. This has made measuring ß a key target for developing observational constraints of the aerosol forcing. While the aerosol burden of the clean, pre-industrial atmosphere has been demonstrated as a key uncertainty for the aerosol forcing, here we show that the behaviour of clouds under these clean conditions is of equal importance for understanding the spread in radiative forcing estimates between models and observations. This means that the uncertainty in the aerosol impact on clouds is, counterintuitively, driven by situations with little aerosol. Discarding clean conditions produces a close agreement between different model and observational estimates of the cloud response to aerosol, but does not provide a strong constraint on the radiative forcing from aerosol-cloud interactions. This makes constraining aerosol behaviour in clean conditions an important goal for future observational studies. [ABSTRACT FROM AUTHOR]

The Copernicus Atmosphere Monitoring Service has recently produced a greenhouse gases reanalysis (version egg4) that covers almost two decades from 2003 to 2020 and will be extended in the future. This reanalysis dataset includes carbon dioxide (CO2) and methane (CH4). The reanalysis procedure combines model data with satellite data into a globally complete and consistent dataset using the European Centre for Medium-range Weather Forecasts' Integrated Forecasting System (IFS). This dataset has been carefully evaluated against independent observations to ensure validity and point out deficiencies to the user. The greenhouse gas reanalysis can be used to examine the impact of atmospheric greenhouse gases concentrations on climate change, such as global and regional climate radiative forcing, assess intercontinental transport, and also serve as boundary conditions for regional simulations, among other applications and scientific studies. The caveats associated with changes in assimilated observations and fixed underlying emissions are highlighted, as well as their impact on the estimation of trends and annual growth rates of these long-lived greenhouse gases. [ABSTRACT FROM AUTHOR]

Retrievals of atmospheric carbon dioxide (C[O.sub.2]) from space-borne measurements of backscattered near-infrared sunlight are hampered by aerosol and cirrus cloud scattering effects. We propose a retrieval approach that allows for the retrieval of a few effective aerosol parameters simultaneously with the C[O.sub.2] total column by parameterizing particle amount, height distribution, and microphysical properties. Two implementations of the proposed method covering different spectral bands are tested for an ensemble of simulated nadir observations for aerosol (and cirrus) loaded scenes over low- and mid-latitudinal land surfaces. The residual aerosol-induced C[O.sub.2] errors are mostly below 1% up to aerosol optical thickness 0.5. The proposed methods also perform convincing for scenes where cirrus clouds of optical thickness 0.1 overlay the aerosol. OCIS codes: 010.0280, 010.1280, 010.1310, 120.6200, 290.1090.

Multi-angle polarimetric (MAP) measurements can enable detailed characterization of aerosol microphysical and optical properties and improve atmospheric correction in ocean color remote sensing. Advanced retrieval algorithms have been developed to obtain multiple geophysical parameters in the atmosphere-ocean system. Theoretical pixel-wise retrieval uncertainties based on error propagation have been used to quantify retrieval performance and determine the quality of data products. However, standard error propagation techniques in high-dimensional retrievals may not always represent true retrieval errors well due to issues such as local minima and nonlinearity of radiative transfer near the solution. In this work, we analyze these theoretical uncertainty estimates and validate them using a flexible Monte Carlo approach. The Fast Multi-Angular Polarimetric Ocean coLor (FastMAPOL) retrieval algorithm, based on several neural network forward models, is used to conduct the retrievals and uncertainty quantification on both synthetic HARP2 (Hyper-Angular Rainbow Polarimeter 2) and AirHARP (airborne version of HARP2) datasets. In addition, for practical application of the technique to uncertainty evaluation in operational data processing, we use the automatic differentiation method to calculate derivatives analytically based on the neural network models. Both the speed and accuracy associated with uncertainty quantification for MAP retrievals are addressed in this study. Pixel-wise retrieval uncertainties are further evaluated for the real AirHARP field campaign data. The uncertainty quantification methods and results can be used to evaluate the quality of data products, and guide MAP algorithm development for current and future satellite systems such as NASA's Plankton, Aerosol, Cloud, ocean Ecosystem (PACE) mission. [ABSTRACT FROM AUTHOR]

We investigate the capabilities of different instrument concepts for the retrieval of aerosol properties over land. It was found that, if the surface reflection properties are unknown, only multiple-viewing-angle measurements of both intensity and polarization are able to provide the relevant aerosol parameters with sufficient accuracy for climate research. Furthermore, retrieval errors are only little affected when the number of viewing angles is increased at the cost of the number of spectral sampling points and vice versa. This indicates that there is a certain amount of freedom for the instrument design of dedicated aerosol instruments. The final choice on the trade-off between the spectral sampling and the number of viewing angles should be made taking other factors into account, such as instrument complexity and the ability to obtain global coverage. OCIS codes: 010.1100, 280.1100, 290.1090, 290.1350.

We present what we believe to be a novel approach to simulating the spectral fine structure ( OCIS codes: 010.0010, 040.1240, 070.4790, 290.5860, 300.6330.

Accurate radiative transfer calculations in cloudy atmospheres are generally time consuming, limiting their practical use in satellite remote sensing applications. We present a model to efficiently calculate the radiative transfer of polarized light in atmospheres that contain homogeneous cloud layers. This model combines the Gauss--Seidel method, which is efficient for inhomogeneous cloudless atmospheres, with the doubling method, which is efficient for homogeneous cloud layers. Additionally to reduce the computational effort for radiative transfer calculations in absorption bands, the cloud reflection and transmission matrices are interpolated over the absorption and scattering optical thicknesses within the cloud layer. We demonstrate that the proposed radiative transfer model in combination with this interpolation technique is efficient for the simulation of satellite measurements for inhomogeneous atmospheres containing one homogeneous cloud layer. For example, the Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) measurements in the oxygen A band (758-773 nm) and the Hartley-Huggins ozone band (295-335 nm) with a spectral resolution of 0.4 nm can be simulated for these atmospheres within 1 min on a 2.8 GHz PC with an accuracy better than 0.1%. OCIS codes: 290.1090, 280.1310, 010.1310, 290.1350.