Abstract

Abstract. As part of the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), we evaluate the historical black carbon (BC) aerosols simulated by 8 ACCMIP models against observations including 12 ice core records, long-term surface mass concentrations, and recent Arctic BC snowpack measurements. We also estimate BC albedo forcing by performing additional simulations using offline models with prescribed meteorology from 1996–2000. We evaluate the vertical profile of BC snow concentrations from these offline simulations using the recent BC snowpack measurements. Despite using the same BC emissions, the global BC burden differs by approximately a factor of 3 among models due to differences in aerosol removal parameterizations and simulated meteorology: 34 Gg to 103 Gg in 1850 and 82 Gg to 315 Gg in 2000. However, the global BC burden from preindustrial to present-day increases by 2.5–3 times with little variation among models, roughly matching the 2.5-fold increase in total BC emissions during the same period. We find a large divergence among models at both Northern Hemisphere (NH) and Southern Hemisphere (SH) high latitude regions for BC burden and at SH high latitude regions for deposition fluxes. The ACCMIP simulations match the observed BC surface mass concentrations well in Europe and North America except at Ispra. However, the models fail to predict the Arctic BC seasonality due to severe underestimations during winter and spring. The simulated vertically resolved BC snow concentrations are, on average, within a factor of 2–3 of the BC snowpack measurements except for Greenland and the Arctic Ocean. For the ice core evaluation, models tend to adequately capture both the observed temporal trends and the magnitudes at Greenland sites. However, models fail to predict the decreasing trend of BC depositions/ice core concentrations from the 1950s to the 1970s in most Tibetan Plateau ice cores. The distinct temporal trend at the Tibetan Plateau ice cores indicates a strong influence from Western Europe, but the modeled BC increases in that period are consistent with the emission changes in Eastern Europe, the Middle East, South and East Asia. At the Alps site, the simulated BC suggests a strong influence from Europe, which agrees with the Alps ice core observations. At Zuoqiupu on the Tibetan Plateau, models successfully simulate the higher BC concentrations observed during the non-monsoon season compared to the monsoon season but overpredict BC in both seasons. Despite a large divergence in BC deposition at two Antarctic ice core sites, some models with a BC lifetime of less than 7 days are able to capture the observed concentrations. In 2000 relative to 1850, globally and annually averaged BC surface albedo forcing from the offline simulations ranges from 0.014 to 0.019 W m−2 among the ACCMIP models. Comparing offline and online BC albedo forcings computed by some of the same models, we find that the global annual mean can vary by up to a factor of two because of different aerosol models or different BC-snow parameterizations and snow cover. The spatial distributions of the offline BC albedo forcing in 2000 show especially high BC forcing (i.e., over 0.1 W m−2) over Manchuria, Karakoram, and most of the Former USSR. Models predict the highest global annual mean BC forcing in 1980 rather than 2000, mostly driven by the high fossil fuel and biofuel emissions in the Former USSR in 1980.

Highlights

  • Black carbon (BC) is defined here as the light-absorbing and refractory portion of carbonaceous aerosols that is emitted through the incomplete combustion of fossil fuel, biofuel, and biomass

  • As part of the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP; Lamarque et al, 2013), our primary goal in this paper is to evaluate preindustrial to present-day black carbon (BC) in ACCMIP models with ice cores sampled from the Arctic, Antarctic, Tibetan Plateau, and Alps

  • We evaluate the present-day BC predictions with long-term atmospheric BC surface mass concentrations and recent BC snowpack measurements from the Arctic regions

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Summary

Introduction

Black carbon (BC) is defined here as the light-absorbing and refractory portion of carbonaceous aerosols that is emitted through the incomplete combustion of fossil fuel, biofuel, and biomass. Filter-based optical instruments such as Particle Soot Absorption Photometer (PSAP) and Aethalometer have been frequently used in long-term atmospheric sampling networks (e.g., Bodhaine, 1995; Sharma et al, 2004) because of ease of remote operation These instruments measure a light absorption coefficient that is converted to BC mass concentrations by. To inter-compare BC models, Koch et al (2009b) evaluated several BC models with available observations including surface mass concentrations, aircraft measurements, aerosol absorption optical depth from AERONET and Ozone Monitoring Instruments, and BC column estimations based on AERONET under the AeroCom model intercomparison project. Since the number of ice cores is limited, our evaluation includes additional BC observations such as a long-term surface mass concentration and BC in snow measurements from the Arctic regions, which are used to compare with the ACCMIP present-day simulations.

Description of ACCMIP models
The offline land and sea-ice models
Global-average BC budgets and spatial distributions
Surface BC mass concentrations and CO mixing ratios
Feb Apr Jun Aug Oct Dec
Present-day BC snow concentrations in the Arctic
BC albedo forcing
Findings
Summary and conclusions
Full Text
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