scholarly journals Radiative Effect and Climate Impacts of Brown Carbon with the Community Atmosphere Model (CAM5)

2018 ◽  
Author(s):  
Hunter Brown ◽  
Xiaohong Liu ◽  
Yan Feng ◽  
Yiquan Jiang ◽  
Mingxuan Wu ◽  
...  

Abstract. A recent development in the representation of aerosols in climate models is the realization that some components of organic aerosol (OA), emitted from biomass and biofuel burning, can have a significant contribution to short-wave radiation absorption in the atmosphere. The absorbing fraction of OA is referred to as brown carbon (BrC). This study introduces one of the first implementations of BrC into the Community Atmosphere Model version 5 (CAM5), using a parameterization for BrC absorptivity described in Saleh et al. (2014). 9-year experiments are run (2003–2011) with prescribed emissions and sea surface temperatures to analyze the effect of BrC in the atmosphere. Model validation is conducted via model comparison to single-scatter albedo and aerosol optical depth from the Aerosol Robotic Network (AERONET). This comparison reveals a model underestimation of SSA in biomass burning regions for both default and BrC model runs, while a comparison between AERONET and model absorption Angstrom exponent shows a marked improvement with BrC implementation. Global annual average radiative effects are calculated due to aerosol-radiation interactions (REari; 0.13 ± 0.01 W m−2) and aerosol-cloud interactions (REaci; 0.01 ± 0.04 W m−2). REari is similar to other studies' estimations of BrC direct radiative effect, while REaci indicates a global reduction in low clouds due to the BrC semi-direct effect. The mechanisms for these physical changes are investigated and found to correspond with changes in global circulation patterns. Comparisons of BrC implementation approaches find that this implementation predicts a lower BrC REari in the Arctic regions than previous studies with CAM5. Implementation of BrC bleaching effect shows a significant reduction in REari (0.06 ± 0.008 W m−2). Also, variations in OA density can lead to differences in REari and REaci, indicating the importance of specifying this property when estimating the BrC radiative effects and when comparing similar studies.

2018 ◽  
Vol 18 (24) ◽  
pp. 17745-17768 ◽  
Author(s):  
Hunter Brown ◽  
Xiaohong Liu ◽  
Yan Feng ◽  
Yiquan Jiang ◽  
Mingxuan Wu ◽  
...  

Abstract. A recent development in the representation of aerosols in climate models is the realization that some components of organic aerosol (OA), emitted from biomass and biofuel burning, can have a significant contribution to shortwave radiation absorption in the atmosphere. The absorbing fraction of OA is referred to as brown carbon (BrC). This study introduces one of the first implementations of BrC into the Community Atmosphere Model version 5 (CAM5), using a parameterization for BrC absorptivity described in Saleh et al. (2014). Nine-year experiments are run (2003–2011) with prescribed emissions and sea surface temperatures to analyze the effect of BrC in the atmosphere. Model validation is conducted via model comparison to single-scatter albedo and aerosol optical depth from the Aerosol Robotic Network (AERONET). This comparison reveals a model underestimation of single scattering albedo (SSA) in biomass burning regions for both default and BrC model runs, while a comparison between AERONET and the model absorption Ångström exponent shows a marked improvement with BrC implementation. Global annual average radiative effects are calculated due to aerosol–radiation interaction (REari; 0.13±0.01 W m−2) and aerosol–cloud interaction (REaci; 0.01±0.04 W m−2). REari is similar to other studies' estimations of BrC direct radiative effect, while REaci indicates a global reduction in low clouds due to the BrC semi-direct effect. The mechanisms for these physical changes are investigated and found to correspond with changes in global circulation patterns. Comparisons of BrC implementation approaches find that this implementation predicts a lower BrC REari in the Arctic regions than previous studies with CAM5. Implementation of BrC bleaching effect shows a significant reduction in REari (0.06±0.008 W m−2). Also, variations in OA density can lead to differences in REari and REaci, indicating the importance of specifying this property when estimating the BrC radiative effects and when comparing similar studies.


2022 ◽  
Author(s):  
Hitoshi Matsui ◽  
Tatsuhiro Mori ◽  
Sho Ohata ◽  
Nobuhiro Moteki ◽  
Naga Oshima ◽  
...  

Abstract. Black carbon (BC) particles in the Arctic contribute to rapid warming of the Arctic by heating the atmosphere and snow and ice surfaces. Understanding the source contributions to Arctic BC is therefore important, but they are not well understood, especially those for atmospheric and snow radiative effects. Here we estimate simultaneously the source contributions of Arctic BC to near-surface and vertically integrated atmospheric BC mass concentrations (MBC_SRF and MBC_COL), BC deposition flux (MBC_DEP), and BC radiative effects at the top of the atmosphere and snow surface (REBC_TOA and REBC_SNOW), and show that the source contributions to these five variables are highly different. In our estimates, Siberia makes the largest contribution to MBC_SRF, MBC_DEP, and REBC_SNOW in the Arctic (defined as > 70° N), accounting for 70 %, 53 %, and 43 %, respectively. In contrast, Asia’s contributions to MBC_COL and REBC_TOA are largest, accounting for 38 % and 45 %, respectively. In addition, the contributions of biomass burning sources are larger (24−34 %) to MBC_DEP, REBC_TOA, and REBC_SNOW, which are highest from late spring to summer, and smaller (4.2−14 %) to MBC_SRF and MBC_COL, whose concentrations are highest from winter to spring. These differences in source contributions to these five variables are due to seasonal variations in BC emission, transport, and removal processes and solar radiation, as well as to differences in radiative effect efficiency (radiative effect per unit BC mass) among sources. Radiative effect efficiency varies by a factor of up to 4 among sources (1465−5439 W g–1) depending on lifetimes, mixing states, and heights of BC and seasonal variations of emissions and solar radiation. As a result, source contributions to radiative effects and mass concentrations (i.e., REBC_TOA and MBC_COL, respectively) are substantially different. The results of this study demonstrate the importance of considering differences in the source contributions of Arctic BC among mass concentrations, deposition, and atmospheric and snow radiative effects for accurate understanding of Arctic BC and its climate impacts.


2013 ◽  
Vol 118 (10) ◽  
pp. 4657-4669 ◽  
Author(s):  
Po-Lun Ma ◽  
Philip J. Rasch ◽  
Hailong Wang ◽  
Kai Zhang ◽  
Richard C. Easter ◽  
...  

2012 ◽  
Vol 5 (3) ◽  
pp. 709-739 ◽  
Author(s):  
X. Liu ◽  
R. C. Easter ◽  
S. J. Ghan ◽  
R. Zaveri ◽  
P. Rasch ◽  
...  

Abstract. A modal aerosol module (MAM) has been developed for the Community Atmosphere Model version 5 (CAM5), the atmospheric component of the Community Earth System Model version 1 (CESM1). MAM is capable of simulating the aerosol size distribution and both internal and external mixing between aerosol components, treating numerous complicated aerosol processes and aerosol physical, chemical and optical properties in a physically-based manner. Two MAM versions were developed: a more complete version with seven lognormal modes (MAM7), and a version with three lognormal modes (MAM3) for the purpose of long-term (decades to centuries) simulations. In this paper a description and evaluation of the aerosol module and its two representations are provided. Sensitivity of the aerosol lifecycle to simplifications in the representation of aerosol is discussed. Simulated sulfate and secondary organic aerosol (SOA) mass concentrations are remarkably similar between MAM3 and MAM7. Differences in primary organic matter (POM) and black carbon (BC) concentrations between MAM3 and MAM7 are also small (mostly within 10%). The mineral dust global burden differs by 10% and sea salt burden by 30–40% between MAM3 and MAM7, mainly due to the different size ranges for dust and sea salt modes and different standard deviations of the log-normal size distribution for sea salt modes between MAM3 and MAM7. The model is able to qualitatively capture the observed geographical and temporal variations of aerosol mass and number concentrations, size distributions, and aerosol optical properties. However, there are noticeable biases; e.g., simulated BC concentrations are significantly lower than measurements in the Arctic. There is a low bias in modeled aerosol optical depth on the global scale, especially in the developing countries. These biases in aerosol simulations clearly indicate the need for improvements of aerosol processes (e.g., emission fluxes of anthropogenic aerosols and precursor gases in developing countries, boundary layer nucleation) and properties (e.g., primary aerosol emission size, POM hygroscopicity). In addition, the critical role of cloud properties (e.g., liquid water content, cloud fraction) responsible for the wet scavenging of aerosol is highlighted.


2019 ◽  
Vol 32 (14) ◽  
pp. 4145-4165 ◽  
Author(s):  
Elizabeth Berry ◽  
Gerald G. Mace ◽  
Andrew Gettelman

Abstract The distribution of clouds and their radiative effects in the Community Atmosphere Model, version 5 (CAM5), are compared to A-Train satellite data in Southeast Asia during the summer monsoon. Cloud radiative kernels are created based on populations of observed and modeled clouds separately in order to compare the sensitivity of the TOA radiation to changes in cloud fraction. There is generally good agreement between the observation- and model-derived cloud radiative kernels for most cloud types, meaning that the clouds in the model are heating and cooling like clouds in nature. Cloud radiative effects are assessed by multiplying the cloud radiative kernel by the cloud fraction histogram. For ice clouds in particular, there is good agreement between the model and observations, with optically thin cirrus producing a moderate warming effect and cirrostratus producing a slight cooling effect, on average. Consistent with observations, the model also shows that the median value of the ice water path (IWP) distribution, rather than the mean, is a more representative measure of the ice clouds that are responsible for heating. In addition, in both observations and the model, it is cirrus clouds with an IWP of 20 g m−2 that have the largest warming effect in this region, given their radiative heating and frequency of occurrence.


2016 ◽  
Author(s):  
Benjamin S. Grandey ◽  
Hsiang-He Lee ◽  
Chien Wang

Abstract. Open-burning fires play an important role in the Earth's climate system. In addition to contributing a substantial fraction of global emissions of carbon dioxide, they are also a major source of atmospheric aerosols such as organic carbon, black carbon, and sulphate. These "fire aerosols" can influence the climate via both direct and indirect radiative effects. In this study, we investigate these radiative effects and the hydrological fast response using the Community Atmosphere Model version 5 (CAM5). Emissions of fire aerosols exert a global mean net radiative effect of −1.0 W m−2, dominated by the cloud shortwave response to organic carbon aerosol. The net radiative effect is particularly strong over boreal regions. By comparing simulations using inter-annually varying versus inter-annually invariant emissions, we find that ignoring the inter-annual variability of the emissions can lead to systematic overestimation of the strength of the net radiative effect of the fire aerosols. Globally, the overestimation is +23 % (−0.2 W m−2). Regionally, the overestimation can be substantially larger. For example, over Australia and New Zealand the overestimation is +58 % (−1.2 W m−2), while over Boreal Asia the overestimation is +43 % (−1.9 W m−2). The systematic overestimation of the net radiative effect of the fire aerosols is likely due to the non-linear influence of aerosols on clouds. However, ignoring inter-annual variability in the emissions does not appear to significantly impact the hydrological fast response. In order to improve understanding of the climate system, we need to more accurately quantify the effects of aerosols, taking into account important characteristics such as inter-annual variability.


2019 ◽  
Author(s):  
Jacob Schacht ◽  
Bernd Heinold ◽  
Johannes Quaas ◽  
John Backman ◽  
Ribu Cherian ◽  
...  

Abstract. Aerosol particles can contribute to the Arctic Amplification by direct and indirect radiative effects. Specifically, black carbon (BC) in the atmosphere, and when deposited on snow and sea ice, has a positive effect on the top of atmosphere radiation balance during polar day. Current climate models, however, are still struggling to reproduce Arctic aerosol conditions. We present an evaluation study with the global aerosol-climate model ECHAM6.3-HAM2.3 to examine emission-related uncertainties in the BC distribution and the direct radiative effect of BC. The model results are comprehensively compared against latest ground and air-borne aerosol observations for the period 2005–2017 with focus on BC. Four different setups of air pollution emissions are tested. The simulations in general match well with the observed amount and temporal variability of near-surface BC in the Arctic. Using actual daily instead of fixed biomass burning emissions is crucial to reproduce individual pollution events but has only a small influence on the seasonal cycle of BC. Compared to commonly used fixed anthropogenic emissions for the year 2000, an up-to-date inventory with transient air pollution emissions results in up to 30 % higher annual BC burden and an over 0.2 W m−2 higher annual mean all-sky net direct radiative effect of BC at top of the atmosphere over the Eastern Arctic Ocean. We estimate BC in the Arctic to lead to a net gain of up 0.8 W m−2 by the direct radiative effect of atmospheric BC plus the effect by an albedo reduction by BC-in-snow. Long-range transport is identified as one of the main sources of uncertainties for ECHAM6.3-HAM2.3, leading to an overestimation of BC in atmospheric layers above 500 hPa especially in summer. This is related to a misrepresentation in wet removal in one identified case at least, that was observed during the ARCTAS summer aircraft campaign. Over all, the current model version has significantly improved since previous intercomparison studies and performs now better than the AeroCom average in terms of the spatial and temporal distribution of Arctic BC.


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