Changes in Atmospheric Constituents and in Radiative Forcing

The Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2), is the latest atmospheric reanalysis of the modern satellite era produced by NASA’s Global Modeling and Assimilation Office (GMAO). MERRA-2 assimilates observation types not available to its predecessor, MERRA, and includes updates to the Goddard Earth Observing System (GEOS) model and analysis scheme so as to provide a viable ongoing climate analysis beyond MERRA’s terminus. While addressing known limitations of MERRA, MERRA-2 is also intended to be a development milestone for a future integrated Earth system analysis (IESA) currently under development at GMAO. This paper provides an overview of the MERRA-2 system and various performance metrics. Among the advances in MERRA-2 relevant to IESA are the assimilation of aerosol observations, several improvements to the representation of the stratosphere including ozone, and improved representations of cryospheric processes. Other improvements in the quality of M...

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The Modern-Era Retrospective Analysis for Research and Applications, Version 2 (MERRA-2)

Black carbon in soot is an efficient absorbing agent of solar irradiation that is preferentially emitted in the tropics and can form atmospheric brown clouds in mixture with other aerosols. These factors combine to make black carbon emissions the second most important contribution to anthropogenic climate warming, after carbon dioxide emissions.

Global and regional climate changes due to black carbon

. The twin Moderate resolution Imaging Spectroradiometer (MODIS) sensors have been flying on Terra since 2000 and Aqua since 2002, creating an extensive data set of global Earth observations. Here, we introduce the Collection 6 (C6) algorithm to retrieve aerosol optical depth (AOD) and aerosol size parameters from MODIS-observed spectral reflectance. While not a major overhaul from the previous Collection 5 (C5) version, there are enough changes that there are significant impacts to the products and their interpretation. The C6 aerosol data set will be created from three separate retrieval algorithms that operate over different surface types. These are the two "Dark Target" (DT) algorithms for retrieving (1) over ocean (dark in visible and longer wavelengths) and (2) over vegetated/dark-soiled land (dark in the visible), plus the "Deep Blue" (DB) algorithm developed originally for retrieving (3) over desert/arid land (bright in the visible). Here, we focus on DT-ocean and DT-land (#1 and #2). We have updated assumptions for central wavelengths, Rayleigh optical depths and gas (H2O, O3, CO2, etc.) absorption corrections, while relaxing the solar zenith angle limit (up to ≤ 84°) to increase poleward coverage. For DT-land, we have updated the cloud mask to allow heavy smoke retrievals, fine-tuned the assignments for aerosol type as function of season/location, corrected bugs in the Quality Assurance (QA) logic, and added diagnostic parameters such topographic altitude. For DT-ocean, improvements include a revised cloud mask for thin-cirrus detection, inclusion of wind speed dependence on the surface reflectance, updates to logic of QA Confidence flag (QAC) assignment, and additions of important diagnostic information. At the same time, we quantified how "upstream" changes to instrument calibration, land/sea masking and cloud masking will also impact the statistics of global AOD, and affect Terra and Aqua differently. For Aqua, all changes will result in reduced global AOD (by 0.02) over ocean and increased AOD (by 0.02) over land, along with changes in spatial coverage. We compared preliminary data to surface-based sun photometer data, and show that C6 should improve upon C5. C6 will include a merged DT/DB product over semi-arid land surfaces for reduced-gap coverage and better visualization, and new information about clouds in the aerosol field. Responding to the needs of the air quality community, in addition to the standard 10 km product, C6 will include a global (DT-land and DT-ocean) aerosol product at 3 km resolution.

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The Collection 6 MODIS aerosol products over land and ocean

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Aerosol cloud precipitation interactions. Part 1. The nature and sources of cloud-active aerosols

Aerosols affect the Earth's energy budget directly by scattering and absorbing radiation and indirectly by acting as cloud condensation nuclei and, thereby, affecting cloud properties. However, large uncertainties exist in current estimates of aerosol forcing because of incomplete knowledge concerning the distribution and the physical and chemical properties of aerosols as well as aerosol-cloud interactions. In recent years, a great deal of effort has gone into improving measurements and datasets. It is thus feasible to shift the estimates of aerosol forcing from largely model-based to increasingly measurement-based. Our goal is to assess current observational capabilities and identify uncertainties in the aerosol direct forcing through comparisons of different methods with independent sources of uncertainties. Here we assess the aerosol optical depth (τ), direct radiative effect (DRE) by natural and anthropogenic aerosols, and direct climate forcing (DCF) by anthropogenic aerosols, focusing on satellite and ground-based measurements supplemented by global chemical transport model (CTM) simulations. The multi-spectral MODIS measures global distributions of aerosol optical depth (τ) on a daily scale, with a high accuracy of ±0.03±0.05τ over ocean. The annual average τ is about 0.14 over global ocean, of which about 21%±7% is contributed by human activities, as estimated by MODIS fine-mode fraction. The multi-angle MISR derives an annual average AOD of 0.23 over global land with an uncertainty of ~20% or ±0.05. These high-accuracy aerosol products and broadband flux measurements from CERES make it feasible to obtain observational constraints for the aerosol direct effect, especially over global the ocean. A number of measurement-based approaches estimate the clear-sky DRE (on solar radiation) at the top-of-atmosphere (TOA) to be about -5.5±0.2 Wm -2 (median ± standard error from various methods) over the global ocean. Accounting for thin cirrus contamination of the satellite derived aerosol field will reduce the TOA DRE to -5.0 Wm -2 . Because of a lack of measurements of aerosol absorption and difficulty in characterizing land surface reflection, estimates of DRE over land and at the ocean surface are currently realized through a combination of satellite retrievals, surface measurements, and model simulations, and are less constrained. Over the oceans the surface DRE is estimated to be -8.8±0.7 Wm -2 . Over land, an integration of satellite retrievals and model simulations derives a DRE of -4.9±0.7 Wm -2 and -11.8±1.9 Wm -2 at the TOA and surface, respectively. CTM simulations derive a wide range of DRE estimates that on average are smaller than the measurement-based DRE by about 30-40%, even after accounting for thin cirrus and cloud contamination. A number of issues remain. Current estimates of the aerosol direct effect over land are poorly constrained. Uncertainties of DRE estimates are also larger on regional scales than on a global scale and large discrepancies exist between different approaches. The characterization of aerosol absorption and vertical distribution remains challenging. The aerosol direct effect in the thermal infrared range and in cloudy conditions remains relatively unexplored and quite uncertain, because of a lack of global systematic aerosol vertical profile measurements. A coordinated research strategy needs to be developed for integration and assimilation of satellite measurements into models to constrain model simulations. Enhanced measurement capabilities in the next few years and high-level scientific cooperation will further advance our knowledge.

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A review of measurement-based assessments of the aerosol direct radiative effect and forcing

[1] An “online” aerosol dynamics and chemistry module is included in the Laboratoire de Meteorologie Dynamique general circulation model (LMDZ), so that the chemical species are advected at each dynamical time step and evolve through chemical and physical processes that have been parameterized consistently with the meteorology These processes include anthropogenic and biogenic emissions, over 50 gas/aqueous phase chemical reactions, transport due to advection, vertical diffusion and convection, dry deposition and wet scavenging We have introduced a size-resolved representation of aerosols which undergo various processes such as coagulation, nucleation and dry and wet scavenging The model considers 16 prognostic tracers: water vapor, liquid water, dimethyl sulfide (DMS), hydrogen sulfide (H2S), dimethyl sulphoxide (DMSO), methanesulphonic acid (MSA), sulfur dioxide (SO2), nitrogen oxides (NOX), carbon monoxide (CO), nitric acid (HNO3), ozone (O3), hydrogen peroxide (H2O2), sulfate mass and number for Aitken and accumulation modes The scheme accounts for two-way interactions between tropospheric chemistry and aerosols The oxidants and chemical species fields that represent the sulfate aerosol formation are evolved interactively with the model dynamics A detailed description on the coupled climate-chemistry interactive module is presented with the evaluation of chemical species in winter and summer seasons Aqueous phase reactions in cloud accounted for 71% of sulfate production rate, while only 45% of the sulfate burden in the troposphere is derived from in-cloud oxidation

https://agupubs.onlinelibrary.wiley.com/doi/pdf/10.1029/2005JD006077

M. S. Reddy

Papers

A review of measurement-based assessments of the aerosol direct radiative effect and forcing

Modeling and analysis of aerosol processes in an interactive chemistry general circulation model