scholarly journals Role of black carbon mass size distribution in the direct aerosol radiative forcing

2019 ◽  
Vol 19 (20) ◽  
pp. 13175-13188 ◽  
Author(s):  
Gang Zhao ◽  
Jiangchuan Tao ◽  
Ye Kuang ◽  
Chuanyang Shen ◽  
Yingli Yu ◽  
...  
Keyword(s):  
Size Distribution ◽  
Black Carbon ◽  
Radiative Forcing ◽  
Climate Models ◽  
Radiative Effects ◽  
Aerosol Radiative Forcing ◽  
Mass Size Distribution ◽  
Mass Size ◽  
Mixing States ◽  
Aerosol Radiative

Abstract. Large uncertainties exist when estimating radiative effects of ambient black carbon (BC) aerosol. Previous studies about the BC aerosol radiative forcing mainly focus on the BC aerosols' mass concentrations and mixing states, while the effects of BC mass size distribution (BCMSD) were not well considered. In this paper, we developed a method of measuring the BCMSD by using a differential mobility analyzer in tandem with an Aethalometer. A comprehensive method of multiple charging corrections was proposed and implemented in measuring the BCMSD. Good agreement was obtained between the BC mass concentration integrated from this system and that measured in the bulk phase, demonstrating the reliability of our proposed method. Characteristics of the BCMSD and corresponding radiative effects were studied based on a field measurement campaign conducted in the North China Plain by using our own measurement system. Results showed that the BCMSD had two modes and the mean peak diameters of the modes were 150 and 503 nm. The BCMSD of the coarser mode varied significantly under different pollution conditions with peak diameter varying between 430 and 580 nm, which gave rise to significant variation in aerosol bulk optical properties. The direct aerosol radiative forcing was estimated to vary by 8.45 % for different measured BCMSDs of the coarser mode, which shared the same magnitude with the variation associated with assuming different aerosol mixing states (10.5 %). Our study reveals that the BCMSD as well as its mixing state in estimating the direct aerosol radiative forcing matters. Knowledge of the BCMSD should be fully considered in climate models.

scholarly journals Role of black carbons mass size distribution in the direct aerosol radiative forcing

2019 ◽  
Author(s):  
Gang Zhao ◽  
Jiangchuan Tao ◽  
Ye Kuang ◽  
Chuanyang Shen ◽  
Yingli Yu ◽  
...  
Keyword(s):  
Size Distribution ◽  
Radiative Forcing ◽  
Climate Models ◽  
Field Measurements ◽  
Radiative Effects ◽  
Aerosol Radiative Forcing ◽  
Mass Size Distribution ◽  
Mass Size ◽  
Mixing States ◽  
Aerosol Radiative

Abstract. Large uncertainties exist when estimating radiative effects of ambient black carbon (BC) aerosol. Previous studies about the BC aerosol radiative forcing mainly focus on the BC aerosols’ mass concentrations and mixing states, while the effects of BC mass size distribution (BCMSD) were not well considered. In this paper, we developed a method by measuring the BCMSD by using a differential mobility analyzer in tandem with an aethalometer. A comprehensive method of multiple charging corrections is proposed and implemented in measuring the BCMSD. Good agreement is obtained between the BC mass concentration integrated from this system and that measured in bulk phase, demonstrating the reliability of our proposed method. Characteristics of the BCMSD and corresponding radiative effects are studied based on field measurements conducted in the North China Plain by using our own designed measurement system. Results show that the BCMSD have two modes and the mean peak diameters of the two modes are 150 nm and 503 nm respectively. The BCMSD of coarser mode varies significantly under different pollution conditions with peak diameter varying between 430 nm and 580 nm, which gives rise to significant variation in aerosol buck optical properties. The aerosol direct aerosol radiative forcing is estimated to vary by 22.5 % for different measured BCMSDs, which shares the same magnitude to the variation associated with assuming different aerosol mixing states (21.5 %). Our study reveals that the BCMSD matters as well as their mixing state in estimating the direct aerosol radiative forcing. Knowledge of the BCMSD should be fully considered in climate models.

Aerosol radiative forcing due to enhanced black carbon at an urban site in India

2002 ◽  
Vol 29 (18) ◽  
pp. 27-1-27-4 ◽  
Author(s):  
S. Suresh Babu ◽  
S. K. Satheesh ◽  
K. Krishna Moorthy
Keyword(s):  
Black Carbon ◽  
Radiative Forcing ◽  
Urban Site ◽  
Aerosol Radiative Forcing ◽  
Aerosol Radiative

scholarly journals Size distribution and coating thickness of black carbon from the Canadian oil sands operations

2017 ◽  
Author(s):  
Yuan Cheng ◽  
Shao-Meng Li ◽  
Mark Gordon ◽  
Peter Liu
Keyword(s):  
Size Distribution ◽  
Black Carbon ◽  
Coating Thickness ◽  
Oil Sands ◽  
Radiative Forcing ◽  
Climate Models ◽  
Source Area ◽  
Size Distributions ◽  
Mixing State ◽  
Earth’S Climate

Abstract. Black carbon (BC) plays an important role in the Earth’s climate system. However, parameterization of BC size and mixing state have not been well addressed in aerosol-climate models, introducing substantial uncertainties into the estimation of radiative forcing by BC. In this study, we focused on BC emissions from the massive oil sands (OS) industry in northern Alberta, based on an aircraft campaign conducted over the Athabasca OS region in 2013. A total of 14 flights were made over the OS source area, in which the aircraft was typically flown in a 4- or 5-sided polygon pattern along flight tracks encircling an OS facility. Another 3 flights were performed downwind of the OS source area, each of which involved at least three intercepting locations where the well-mixed OS plume was measured along flight tracks perpendicular to the wind direction. Comparable size distributions were observed for refractory black carbon (rBC) over and downwind of the OS facilities, with rBC mass median diameters (MMD) between ~ 135 and 145 nm that were characteristic of fresh urban emissions. This MMD range corresponded to rBC number median diameters (NMD) of ~ 60–70 nm, approximately 100 % higher than the NMD settings in some aerosol-climate models. The typical in- and out-of-plume segments of a flight, which had different rBC concentrations and photochemical ages, showed consistent rBC size distributions. Moreover, rBC size distributions remained unchanged at different downwind distances from the source area, suggesting that atmospheric aging would not necessarily change rBC size distribution. However, aging indeed influenced rBC mixing state. Coating thickness for rBC cores in the diameter range of 130–160 nm was nearly doubled within three hours when the OS plume was transported over a distance of 90 km from the source area.

scholarly journals Wet removal of black carbon in Asian outflow: Aerosol Radiative Forcing in East Asia (A-FORCE) aircraft campaign

2012 ◽  
Vol 117 (D3) ◽  
pp. n/a-n/a ◽  
Author(s):  
N. Oshima ◽  
Y. Kondo ◽  
N. Moteki ◽  
N. Takegawa ◽  
M. Koike ◽  
...  
Keyword(s):  
East Asia ◽  
Black Carbon ◽  
Radiative Forcing ◽  
Aerosol Radiative Forcing ◽  
Aerosol Radiative ◽  
Wet Removal

Constraining direct aerosol radiative forcing using remote sensing and in-situ constraints

2020 ◽  
Author(s):  
Lucia Timea Deaconu ◽  
Duncan Watson-Parris ◽  
Philip Stier ◽  
Lindsay Lee
Keyword(s):  
Remote Sensing ◽  
Black Carbon ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Removal Rates ◽  
Aerosol Radiative Forcing ◽  
Aerosol Absorption ◽  
Direct Radiative Forcing ◽  
Aerosol Radiative

<p>Absorbing aerosols affect the climate system (radiative forcing, cloud formation, precipitation and more) by strongly absorbing solar radiation, particularly at ultraviolet and visible wavelengths. The environmental impacts of an absorbing aerosol layer are influenced by its single scattering albedo (SSA), the albedo of the underlying surface, and also by the atmospheric residence time and column concentration of the aerosols.</p><p>Black-carbon (BC), the collective term used for strongly absorbing, carbonaceous aerosols, emitted by incomplete combustion of fossil fuel, biofuel and biomass, is a significant contributor to atmospheric absorption and probably a main-driver in inter-model differences and large uncertainties in estimating the aerosol radiative forcing due to aerosol-radiation interaction (RFari). Estimates of BC direct radiative forcing suggest a positive effect of +0.71 Wm<sup>-2</sup> (Bond and Bergstrom (2006)) with large uncertainties [+0.08, +1.27] Wm<sup>-2</sup>. These uncertainties result from poor estimates of BC atmospheric burden (emissions and removal rates) and its radiative properties. The uncertainty in the burden is due to the uncertainty in emissions (7.5 [2, 29] Tg yr<sup>-1</sup>) and lifetime (removal rates). In comparison with the available observations, global climate models (GCMs) tend to under-predict absorption near source (e.g. at AERONET stations), and over-predict concentrations in remote regions (e.g. as measured by aircraft campaigns). This may be due to GCM’s weak emissions at the source, but longer lifetime of aerosols in the atmosphere.</p><p>This study aims to address the parametric uncertainty of GCMs and constrain the direct radiative forcing using a perturbed parameter ensemble (PPE) and a collection of observations, from remote sensing to in-situ measurements. Total atmospheric aerosol extinction is quantified using satellite observations that provide aerosol optical depth (AOD), while the SSA is constrained by the use of high-temporal resolution aerosol absorption optical depth (AAOD) measured with AERONET sun-photometers (for near-source columnar information of aerosol absorption) and airborne black-carbon in-situ measurements collected and synthesised in the Global Aerosol Synthesis and Science Project (GASSP) (for properties of long-range transported aerosols). Measurements from the airborne campaigns ATOM and HIPPO are valuable for constraining aerosol absorption in remote areas, while CLARIFY and ORACLES, that were employed over Southeast Atlantic, are considered in our study for near source observations of biomass burning aerosols transported over the bright surface of stratocumulus clouds.</p><p>Using the PPE to explore the uncertainties in the aerosol absorption as well as the dominant emission and removal processes, and by comparing with a variety of observations we have confidence to better constrain the aerosol direct radiative forcing.</p>

scholarly journals Dust aerosol radiative effects during summer 2012 simulated with a coupled regional aerosol–atmosphere–ocean model over the Mediterranean

2015 ◽  
Vol 15 (6) ◽  
pp. 3303-3326 ◽  
Author(s):  
P. Nabat ◽  
S. Somot ◽  
M. Mallet ◽  
M. Michou ◽  
F. Sevault ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Mediterranean Region ◽  
Short Wave ◽  
Ocean Model ◽  
Dust Particles ◽  
Radiative Effects ◽  
Aerosol Radiative Forcing ◽  
Dust Aerosols ◽  
The Mediterranean ◽  
Aerosol Radiative

Abstract. The present study investigates the radiative effects of dust aerosols in the Mediterranean region during summer 2012 using a coupled regional aerosol–atmosphere–ocean model (CNRM-RCSM5). A prognostic aerosol scheme, including desert dust, sea salt, organic, black-carbon and sulphate particles, has been integrated to CNRM-RCSM5 in addition to the atmosphere, land surface and ocean components. An evaluation of this aerosol scheme of CNRM-RCSM5, and especially of the dust aerosols, has been performed against in situ and satellite measurements, showing its ability to reproduce the spatial and temporal variability of aerosol optical depth (AOD) over the Mediterranean region in summer 2012. The dust vertical and size distributions have also been evaluated against observations from the TRAQA/ChArMEx campaign. Three simulations have been carried out for summer 2012 with CNRM-RCSM5, including the full prognostic aerosol scheme, only monthly-averaged AOD means from the aerosol scheme or no aerosols at all, in order to focus on the radiative effects of dust particles and the role of the prognostic scheme. Surface short-wave aerosol radiative forcing variability is found to be more than twice as high over regions affected by dust aerosols, when using a prognostic aerosol scheme instead of monthly AOD means. In this case downward surface solar radiation is also found to be better reproduced according to a comparison with several stations across the Mediterranean. A composite study over 14 stations across the Mediterranean, designed to identify days with high dust AOD, also reveals the improvement of the representation of surface temperature brought by the use of the prognostic aerosol scheme. Indeed the surface receives less radiation during dusty days, but only the simulation using the prognostic aerosol scheme is found to reproduce the observed intensity of the dimming and warming on dusty days. Moreover, the radiation and temperature averages over summer 2012 are also modified by the use of prognostic aerosols, mainly because of the differences brought in short-wave aerosol radiative forcing variability. Therefore this first comparison over summer 2012 highlights the importance of the choice of the representation of aerosols in climate models.

scholarly journals Quantifying uncertainty from aerosol and atmospheric parameters and their impact on climate sensitivity

2018 ◽  
Vol 18 (23) ◽  
pp. 17529-17543 ◽  
Author(s):  
Christopher G. Fletcher ◽  
Ben Kravitz ◽  
Bakr Badawy
Keyword(s):  
Black Carbon ◽  
Climate Sensitivity ◽  
Radiative Forcing ◽  
Deep Convection ◽  
Cloud Amount ◽  
Skill Score ◽  
Model Parameters ◽  
Atmospheric Parameters ◽  
Aerosol Radiative Forcing ◽  
Aerosol Radiative

Abstract. Climate sensitivity in Earth system models (ESMs) is an emergent property that is affected by structural (missing or inaccurate model physics) and parametric (variations in model parameters) uncertainty. This work provides the first quantitative assessment of the role of compensation between uncertainties in aerosol forcing and atmospheric parameters, and their impact on the climate sensitivity of the Community Atmosphere Model, Version 4 (CAM4). Running the model with prescribed ocean and ice conditions, we perturb four parameters related to sulfate and black carbon aerosol radiative forcing and distribution, as well as five atmospheric parameters related to clouds, convection, and radiative flux. In this experimental setup where aerosols do not affect the properties of clouds, the atmospheric parameters explain the majority of variance in climate sensitivity, with two parameters being the most important: one controlling low cloud amount, and one controlling the timescale for deep convection. Although the aerosol parameters strongly affect aerosol optical depth, their impacts on climate sensitivity are substantially weaker than the impacts of the atmospheric parameters, but this result may depend on whether aerosol–cloud interactions are simulated. Based on comparisons to inter-model spread of other ESMs, we conclude that structural uncertainties in this configuration of CAM4 likely contribute 3 times more to uncertainty in climate sensitivity than parametric uncertainties. We provide several parameter sets that could provide plausible (measured by a skill score) configurations of CAM4, but with different sulfate aerosol radiative forcing, black carbon radiative forcing, and climate sensitivity.

scholarly journals Single particle characterization of black carbon aerosol in the Northeast Tibetan Plateau, China

2012 ◽  
Vol 12 (8) ◽  
pp. 21947-21976 ◽  
Author(s):  
Q. Y. Wang ◽  
J. P. Schwarz ◽  
J. J. Cao ◽  
R. S. Gao ◽  
D. W. Fahey ◽  
...  
Keyword(s):  
Tibetan Plateau ◽  
Size Distribution ◽  
Black Carbon ◽  
Single Particle ◽  
Qinghai Lake ◽  
Equivalent Diameter ◽  
The Tibetan Plateau ◽  
Mass Size Distribution ◽  
Low Concentrations ◽  
Mass Size

Abstract. Refractory black carbon (rBC) mass, size distribution, and mixing state were measured with a ground-based Single Particle Soot Photometer (SP2) at Qinghai Lake (QHL), a rural area in the Northeastern Tibetan Plateau of China, during October 2011. The average measured rBC mass concentration of 0.36 μg STP-m−3 is significantly higher than the concentrations measured in background and remote regions around the globe. The diurnal variation of rBC concentration showed nocturnal peak and afternoon low concentrations and showed a loose anticorrelation to the variation of mixed layer depths, indicating nighttime trapping of emissions and daytime ventilation. The high rBC values and their diurnal behavior strongly suggest that the QHL area was heavily influenced by local rBC sources. The mass size distribution of rBC showed a primary mode peak at 175-nm diameter and a small secondary mode peak at 495 nm volume-equivalent diameter assuming 2 g cm−3 void free density. About 40% of the observed rBC particles within the detectable size range were mixed with large amounts of non-refractory materials present as a thick coating. A comparison of the Aethalometer and SP2 measurements suggests that there are non-BC species strongly affecting the Aethalometer measurement and, therefore, the Aethalometer measurements are not reliable for rBC determinations in the Tibetan Plateau region without artifact corrections. The apparent black-carbon specific, mass-absorption cross section derived from the Aethalometer and SP2 data was 37.5 m2 g−1 at a wavelength of 880 nm. A strong correlation was found between rBC and CO with a slope of 1.5 ± 0.1 ng STP-m−3 ppbv−1, similar to values of mixed rural emissions.

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