scholarly journals Contribution of primary carbonaceous aerosol to cloud condensation nuclei: processes and uncertainties evaluated with a global aerosol microphysics model

2007 ◽  
Vol 7 (20) ◽  
pp. 5447-5466 ◽  
Author(s):  
J. R. Pierce ◽  
K. Chen ◽  
P. J. Adams
Keyword(s):  
Size Distribution ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Global Climate Model ◽  
Organic Aerosol ◽  
Carbonaceous Aerosol ◽  
Condensation Nuclei ◽  
Carbonaceous Particles ◽  
Seeding Effect ◽  
Inorganic Aerosol

Abstract. This paper explores the impacts of primary carbonaceous aerosol on cloud condensation nuclei (CCN) concentrations in a global climate model with size-resolved aerosol microphysics. Organic matter (OM) and elemental carbon (EC) from two emissions inventories were incorporated into a preexisting model with sulfate and sea-salt aerosol. The addition of primary carbonaceous aerosol increased CCN(0.2%) concentrations by 65–90% in the globally averaged surface layer depending on the carbonaceous emissions inventory used. Sensitivity studies were performed to determine the relative importance of organic solubility/hygroscopicity in predicting CCN. In a sensitivity study where carbonaceous aerosol was assumed to be completely insoluble, concentrations of CCN(0.2%) still increased by 40–50% globally over the no carbonaceous simulation because primary carbonaceous emissions were able to become CCN via condensation of sulfuric acid. This shows that approximately half of the contribution of primary carbonaceous particles to CCN in our model comes from the addition of new particles (seeding effect) and half from the contribution of organic solute (solute effect). The solute effect tends to dominate more in areas where there is less inorganic aerosol than organic aerosol and the seeding effect tends to dominate in areas where there is more inorganic aerosol than organic aerosol. It was found that an accurate simulation of the number size distribution is necessary to predict the CCN concentration but assuming an average chemical composition will generally give a CCN concentration within a factor of 2. If a "typical" size distribution is assumed for each species when calculating CCN, such as is done in bulk aerosol models, the mean error relative to a simulation with size resolved microphysics is on the order of 35%. Predicted values of carbonaceous aerosol mass and aerosol number were compared to observations and the model showed average errors of a factor of 3 for carbonaceous mass and a factor of 4 for total aerosol number; however, errors in the accumulation mode concentrations were found to be lower in comparisons with European and marine observations.. The errors in CN and carbonaceous mass may be reduced by improving the emission size distributions of both primary sulfate and primary carbonaceous aerosol.

scholarly journals Contribution of carbonaceous aerosol to cloud condensation nuclei: processes and uncertainties evaluated with a global aerosol microphysics model

2007 ◽  
Vol 7 (3) ◽  
pp. 7723-7765 ◽  
Author(s):  
J. R. Pierce ◽  
K. Chen ◽  
P. J. Adams
Keyword(s):  
Size Distribution ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Global Climate Model ◽  
Organic Aerosol ◽  
Carbonaceous Aerosol ◽  
Condensation Nuclei ◽  
Carbonaceous Particles ◽  
Seeding Effect ◽  
Inorganic Aerosol

Abstract. This paper explores the impacts of carbonaceous aerosol on cloud condensation nuclei (CCN) concentrations in a global climate model with size-resolved aerosol microphysics. Organic matter (OM) and elemental carbon (EC) from two emissions inventories were incorporated into a preexisting model with sulfate and sea-salt aerosol. The addition of carbonaceous aerosol increased CCN(0.2%) concentrations by 65–90% in the globally averaged surface layer depending on the carbonaceous emissions inventory used. Sensitivity studies were performed to determine the relative importance of the organic "solute effect", in which CCN concentrations increase because of the added soluble carbonaceous material, versus the "seeding effect", in which CCN concentrations increase because of increased particle number concentrations. In a sensitivity study where carbonaceous aerosol was assumed to be completely insoluble, concentrations of CCN(0.2%) still increased by 40–50% globally over the no carbonaceous simulation because primary carbonaceous emissions were able to become CCN via condensation of sulfuric acid. This shows that approximately half of the contribution of carbonaceous particles to CCN comes from the "seeding effect" and half from the "solute effect". The solute effect tends to dominate more in areas where there is less inorganic aerosol than organic aerosol and the seeding effect tends to dominate in areas where is more inorganic aerosol than organic aerosol. It was found that an accurate simulation of the number size distribution is necessary to predict the CCN concentration but assuming an average chemical composition will generally give a CCN concentration within a factor of 2. If a "typical" size distribution is assumed for each species when calculating CCN, such as is done in bulk aerosol models, the mean error relative to a simulation with size resolved microphysics is on the order of 35%. Predicted values of carbonaceous aerosol mass and aerosol number were compared to observations and the model showed average errors of a factor of 3 for carbonaceous mass and a factor of 4 for total aerosol number. These errors may be reduced by improving the emission size distributions of both primary sulfate and primary carbonaceous aerosol.

The effect of the photomineralization mechanism on ambient organic aerosols' cloud condensation nuclei and ice nucleation abilities

2020 ◽  
Author(s):  
Silvan Müller ◽  
Nadine Borduas-Dedekind
Keyword(s):  
Climate Model ◽  
Global Climate ◽  
Cloud Condensation Nuclei ◽  
Global Climate Model ◽  
Complex Mixture ◽  
Substantial Effect ◽  
Ice Nucleation ◽  
Anthropogenic Sources ◽  
Wood Smoke ◽  
Condensation Nuclei

<p>Organic aerosol (OA) is an important component of the atmospheric submicron particulate mass, consisting of a complex mixture of organic compounds from natural and anthropogenic sources. During its lifetime of approximately one week in the atmosphere, OA is exposed to sunlight and thus undergoes atmospheric processing through photochemistry. This photochemical aging mechanism is thought to have a substantial effect on the propensity of OA to participate in cloud-forming processes by increasing its cloud condensation nuclei (CCN) activity. However, this effect is not well-constrained, and the influence of photochemistry on the ice nucleation (IN) activity of OA is uncertain. In this study, we aim to better understand how the photomineralization mechanism changes the cloud-forming properties of OA by measuring the CCN and IN abilities of photochemically aged OA of different sources: (1) Laboratory-generated ammonium sulfate-methylglyoxal (a proxy for secondary OA), and ambient OA bulk solutions collected from (2) wood smoke and (3) urban particulate matter in Padua (Italy). The solutions are exposed to UV-B radiation in a photoreactor for up to 25 hour and subsequently analyzed for their IN ability and, following aerosolization, for their CCN ability. To correlate changes in cloud-forming properties with changes in chemical composition due to photomineralization, we measure total organic carbon, UV-Vis absorbance, and CO, CO<sub>2</sub>, acetic acid, formic acid, pyruvic acid and oxalic acid production. Indeed, preliminary data of wood smoke OA highlights photomineralization as an important atmospheric aging process that modifies the CCN ability of OA. By characterizing both the CCN and IN abilities of photochemically aged OA, our study may thus provide important insights into the atmospheric evolution and cloud-forming properties of OA, potentially establishing photomineralization of OA as an important mechanism to consider in regional and global climate model predictions.</p>

scholarly journals Organic aerosol and global climate modelling: a review

2005 ◽  
Vol 5 (4) ◽  
pp. 1053-1123 ◽  
Author(s):  
M. Kanakidou ◽  
J. H. Seinfeld ◽  
S. N. Pandis ◽  
I. Barnes ◽  
F. J. Dentener ◽  
...  
Keyword(s):  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Organic Aerosol ◽  
Climate Impact ◽  
Climate Modelling ◽  
Carbonaceous Particles ◽  
Global Climate Modelling ◽  
Removal Processes ◽  
Wet Removal

Abstract. The present paper reviews existing knowledge with regard to Organic Aerosol (OA) of importance for global climate modelling and defines critical gaps needed to reduce the involved uncertainties. All pieces required for the representation of OA in a global climate model are sketched out with special attention to Secondary Organic Aerosol (SOA): The emission estimates of primary carbonaceous particles and SOA precursor gases are summarized. The up-to-date understanding of the chemical formation and transformation of condensable organic material is outlined. Knowledge on the hygroscopicity of OA and measurements of optical properties of the organic aerosol constituents are summarized. The mechanisms of interactions of OA with clouds and dry and wet removal processes parameterisations in global models are outlined. This information is synthesized to provide a continuous analysis of the flow from the emitted material to the atmosphere up to the point of the climate impact of the produced organic aerosol. The sources of uncertainties at each step of this process are highlighted as areas that require further studies.

scholarly journals Organic aerosol and global climate modelling: a review

2004 ◽  
Vol 4 (5) ◽  
pp. 5855-6024 ◽  
Author(s):  
M. Kanakidou ◽  
J. H. Seinfeld ◽  
S. N. Pandis ◽  
I. Barnes ◽  
F. J. Dentener ◽  
...  
Keyword(s):  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Organic Aerosol ◽  
Climate Impact ◽  
Climate Modelling ◽  
Carbonaceous Particles ◽  
Global Climate Modelling ◽  
Removal Processes ◽  
Wet Removal

Abstract. The present paper reviews existing knowledge with regard to Organic Aerosol (OA) of importance for global climate modelling and defines critical gaps needed to reduce the involved uncertainties. All pieces required for the representation of OA in a global climate model are sketched out with special attention to Secondary Organic Aerosol (SOA): The emission estimates of primary carbonaceous particles and SOA precursor gases are summarized. The up-to-date understanding of the chemical formation and transformation of condensable organic material is outlined. Knowledge on the hygroscopicity of OA and measurements of optical properties of the organic aerosol constituents are summarized. The mechanisms of interactions of OA with clouds and dry and wet removal processes parameterisations in global models are outlined. This information is synthesized to provide a continuous analysis of the flow from the emitted material to the atmosphere up to the point of the climate impact of the produced organic aerosol. The sources of uncertainties at each step of this process are highlighted as areas that require further studies.

scholarly journals Does the POA–SOA split matter for global CCN formation?

2014 ◽  
Vol 14 (2) ◽  
pp. 995-1010 ◽  
Author(s):  
W. Trivitayanurak ◽  
P. J. Adams
Keyword(s):  
Chemical Composition ◽  
Transport Model ◽  
Climate Modeling ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Carbonaceous Aerosols ◽  
Chemical Transport Model ◽  
Condensation Nuclei ◽  
Carbonaceous Particles ◽  
Microphysical Processes

Abstract. A model of carbonaceous aerosols has been implemented in the TwO-Moment Aerosol Sectional (TOMAS) microphysics module in the GEOS-Chem chemical transport model (CTM), a model driven by assimilated meteorology. Inclusion of carbonaceous emissions alongside pre-existing treatments of sulfate and sea-salt aerosols increases the number of emitted primary aerosol particles by a factor of 2.5 and raises annual-average global cloud condensation nuclei at 0.2% supersaturation (CCN(0.2%)) concentrations by a factor of two. Compared to the prior model without carbonaceous aerosols, this development improves the model prediction of condensation nuclei with dry diameter larger than 10 nm (CN10) number concentrations significantly from −45% to −7% bias when compared to long-term observations. Inclusion of carbonaceous particles also largely eliminates a tendency for the model to underpredict higher cloud condensation nuclei (CCN) concentrations. Similar to other carbonaceous models, the model underpredicts organic carbon (OC) and elemental carbon (EC) mass concentrations by a factor of 2 when compared to EMEP and IMPROVE observations. Because primary organic aerosol (POA) and secondary organic aerosol (SOA) affect aerosol number size distributions via different microphysical processes, we assess the sensitivity of CCN production, for a fixed source of organic aerosol (OA) mass, to the assumed POA–SOA split in the model. For a fixed OA budget, we found that CCN(0.2%) decreases nearly everywhere as the model changes from a world dominated by POA emissions to one dominated by SOA condensation. POA is about twice as effective per unit mass at CCN production compared to SOA. Changing from a 100% POA scenario to a 100% SOA scenario, CCN(0.2%) concentrations in the lowest model layer decrease by about 20%. In any scenario, carbonaceous aerosols contribute significantly to global CCN. The SOA–POA split has a significant effect on global CCN, and the microphysical implications of POA emissions versus SOA condensation appear to be at least as important as differences in chemical composition as expressed by the hygroscopicity of OA. These findings stress the need to better understand carbonaceous aerosols loadings, the global SOA budget, microphysical pathways of OA formation (emissions versus condensation) as well as chemical composition to improve climate modeling.

scholarly journals Intercomparison of modal and sectional aerosol microphysics representations within the same 3-D global chemical transport model

2012 ◽  
Vol 12 (1) ◽  
pp. 623-689 ◽  
Author(s):  
G. W. Mann ◽  
K. S. Carslaw ◽  
D. A. Ridley ◽  
D. V. Spracklen ◽  
K. J. Pringle ◽  
...  
Keyword(s):  
Size Distribution ◽  
Transport Model ◽  
Cloud Condensation Nuclei ◽  
Particle Growth ◽  
Free Troposphere ◽  
Chemical Transport Model ◽  
Condensation Nuclei ◽  
Chemistry Transport Model ◽  
Surface Mass ◽  
Cloud Processing

Abstract. A global modal aerosol microphysics module (GLOMAP-mode) is evaluated and improved by comparing against a sectional version (GLOMAP-bin) and observations in the same 3-D global offline chemistry transport model. With both schemes, the model captures the main features of the global particle size distribution, with sub-micron aerosol approximately unimodal in continental regions and bi-modal in marine regions. Initial bin-mode comparisons showed that various size distribution parameter settings (mode widths and inter-modal separation sizes) resulted in clear biases compared to the sectional scheme. By adjusting these parameters in the modal scheme, much better agreement is achieved against the bin scheme and observations. Surface mass of sulphate, sea-salt, black carbon (BC) and organic carbon (OC) are, on the annual mean, within 25 % in the two schemes in nearly all regions. On the annual mean, surface level concentrations of condensation nuclei (CN), cloud condensation nuclei (CCN), surface area density and condensation sink also compare within 25 % in most regions. However, marine CCN concentrations between 30° N and 30° S are systematically higher in the modal scheme, by 25–60 %, which we attribute to differences in size-resolved particle growth or cloud-processing. Larger differences also exist in regions or seasons dominated by biomass burning and in free-troposphere and high-latitude regions. Indeed, in the free-troposphere, GLOMAP-mode BC is a factor 2–4 higher than GLOMAP-bin, likely due to differences in size-resolved scavenging. Nevertheless, in most parts of the atmosphere, we conclude that bin-mode differences are much less than model-observation differences, although some processes are missing in these runs which may pose a bigger challenge to modal schemes (e.g. boundary layer nucleation, ultra-fine sea-spray). The findings here underline the need for a spectrum of complexity in global models, with size-resolved aerosol properties predicted by modal schemes needing to be continually benchmarked and improved against freely evolving sectional schemes and observations.

scholarly journals Comparison of ice particle characteristics simulated by the Community Atmosphere Model (CAM5) with in-situ observations

2014 ◽  
Vol 14 (6) ◽  
pp. 7637-7681 ◽  
Author(s):  
T. Eidhammer ◽  
H. Morrison ◽  
A. Bansemer ◽  
A. Gettelman ◽  
A. J. Heymsfield
Keyword(s):  
Size Distribution ◽  
Radiative Forcing ◽  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Atmospheric Model ◽  
Slope Parameter ◽  
Cloud Radiative Forcing ◽  
Threshold Size ◽  
Cloud Ice

Abstract. Detailed measurements of ice crystals in cirrus clouds were used to compare with results from the Community Atmospheric Model Version 5 (CAM5) global climate model. The observations are from two different field campaigns with contrasting conditions: Atmospheric Radiation Measurements Spring Cloud Intensive Operational Period in 2000 (ARM-IOP), which was characterized primarily by midlatitude frontal clouds and cirrus, and Tropical Composition, Cloud and Climate Coupling (TC4), which was dominated by anvil cirrus. Results show that the model typically overestimates the slope parameter of the exponential size distributions of cloud ice and snow, while the variation with temperature (height) is comparable. The model also overestimates the ice/snow number concentration (0th moment of the size distribution) and underestimates higher moments (2nd through 5th), but compares well with observations for the 1st moment. Overall the model shows better agreement with observations for TC4 than for ARM-IOP in regards to the moments. The mass-weighted terminal fallspeed is lower in the model compared to observations for both ARM-IOP and TC4, which is partly due to the overestimation of the size distribution slope parameter. Sensitivity tests with modification of the threshold size for cloud ice to snow autoconversion (Dcs) do not show noticeable improvement in modeled moments, slope parameter and mass weighed fallspeed compared to observations. Further, there is considerable sensitivity of the cloud radiative forcing to Dcs, consistent with previous studies, but no value of Dcs improves modeled cloud radiative forcing compared to measurements. Since the autoconversion of cloud ice to snow using the threshold size Dcs has little physical basis, future improvement to combine cloud ice and snow into a single category, eliminating the need for autoconversion, is suggested.

scholarly journals Estimating cloud condensation nuclei number concentrations using aerosol optical properties: role of particle number size distribution and parameterization

2019 ◽  
Vol 19 (24) ◽  
pp. 15483-15502 ◽  
Author(s):  
Yicheng Shen ◽  
Aki Virkkula ◽  
Aijun Ding ◽  
Krista Luoma ◽  
Helmi Keskinen ◽  
...  
Keyword(s):  
Optical Properties ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Size Distributions ◽  
Condensation Nuclei ◽  
Aerosol Optical Properties ◽  
Average Bias ◽  
Angstrom Exponent ◽  
Ångström Exponent ◽  
Ångstrom Exponent

Abstract. The concentration of cloud condensation nuclei (CCN) is an essential parameter affecting aerosol–cloud interactions within warm clouds. Long-term CCN number concentration (NCCN) data are scarce; there are a lot more data on aerosol optical properties (AOPs). It is therefore valuable to derive parameterizations for estimating NCCN from AOP measurements. Such parameterizations have already been made, and in the present work a new parameterization is presented. The relationships between NCCN, AOPs, and size distributions were investigated based on in situ measurement data from six stations in very different environments around the world. The relationships were used for deriving a parameterization that depends on the scattering Ångström exponent (SAE), backscatter fraction (BSF), and total scattering coefficient (σsp) of PM10 particles. The analysis first showed that the dependence of NCCN on supersaturation (SS) can be described by a logarithmic fit in the range SS <1.1 %, without any theoretical reasoning. The relationship between NCCN and AOPs was parameterized as NCCN≈((286±46)SAE ln(SS/(0.093±0.006))(BSF − BSFmin) + (5.2±3.3))σsp, where BSFmin is the minimum BSF, in practice the 1st percentile of BSF data at a site to be analyzed. At the lowest supersaturations of each site (SS ≈0.1 %), the average bias, defined as the ratio of the AOP-derived and measured NCCN, varied from ∼0.7 to ∼1.9 at most sites except at a Himalayan site where the bias was >4. At SS >0.4 % the average bias ranged from ∼0.7 to ∼1.3 at most sites. For the marine-aerosol-dominated site Ascension Island the bias was higher, ∼1.4–1.9. In other words, at SS >0.4 % NCCN was estimated with an average uncertainty of approximately 30 % by using nephelometer data. The biases were mainly due to the biases in the parameterization related to the scattering Ångström exponent (SAE). The squared correlation coefficients between the AOP-derived and measured NCCN varied from ∼0.5 to ∼0.8. To study the physical explanation of the relationships between NCCN and AOPs, lognormal unimodal particle size distributions were generated and NCCN and AOPs were calculated. The simulation showed that the relationships of NCCN and AOPs are affected by the geometric mean diameter and width of the size distribution and the activation diameter. The relationships of NCCN and AOPs were similar to those of the observed ones.

scholarly journals Nucleation-mode particle pool and large increases in <i>N</i><sub>cn</sub> and <i>N</i><sub>ccn</sub> observed over the northwestern Pacific Ocean in the spring of 2014

2019 ◽  
Vol 19 (13) ◽  
pp. 8845-8861 ◽  
Author(s):  
Juntao Wang ◽  
Yanjie Shen ◽  
Kai Li ◽  
Yang Gao ◽  
Huiwang Gao ◽  
...  
Keyword(s):  
Pacific Ocean ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Number Concentration ◽  
Atmospheric Particles ◽  
Northwestern Pacific ◽  
Condensation Nuclei ◽  
Northwestern Pacific Ocean ◽  
Mean Values ◽  
Nucleation Mode

Abstract. Determination of the updated concentrations of atmospheric particles (Ncn) and the concentrations of cloud condensation nuclei (Nccn) over the northwestern Pacific Ocean (NWPO) are important to accurately evaluate the influence of aerosol outflow from the Asian continent on the climate by considering the rapid changes in emissions of air pollutants therein. However, field observations in the last two decades are scarce. We conducted a cruise campaign over the NWPO to simultaneously measure Ncn, Nccn and the size distribution of aerosol particles from day of year (DOY) 81 to DOY 108 of 2014. The mean values of Nccn at supersaturation (SS) of levels 0.2 % and 0.4 % were 0.68±0.38×103 and 1.1±0.67×103 cm−3, respectively, with an average of 2.8±1.0×103 cm−3 for Ncn during the cruise over the NWPO. All are approximately 1 order of magnitude larger than spring observations made during the preceding two decades in the remote marine atmosphere. The larger values, against the marine natural background reported in the literature, imply an overwhelming contribution from continental inputs. The calculated activity ratios (ARs) of the cloud condensation nuclei (CCN) were 0.30±0.11 and 0.46±0.19 at SS levels of 0.2 % and 0.4 %, respectively, which are almost the same as those of upwind semi-urban sites. High Nccn and CCN activities were observed from DOY 98 to DOY 102, when the oceanic zone received even stronger continental input. Excluding biomass burning (BB) and dust aerosols, good correlation between Nccn at 0.4 % SS and the number concentrations of > 60 nm particles (N>60 nm) was obtained during the entire cruise period, with a slope of 0.98 and R2=0.94, and the corresponding effective hygroscopicity parameter (κ) was estimated to be 0.40. A bimodal size distribution pattern of the particle number concentration was generally observed during the entire campaign when the N>90 nm varied largely. However, the N<30 nm, accounting for approximately one-third of the total number concentration, varied narrowly, and two NPF events associated with vertical transport were observed. This implies that a pool of nucleation-mode atmospheric particles is aloft. BB and dust events were observed over the NWPO, but their aerosol contributions to Ncn and Nccn were minor (i.e., 10 % or less) on a monthly timescale.

scholarly journals Combustion Organic Aerosol as Cloud Condensation Nuclei in Ship Tracks

2000 ◽  
Vol 57 (16) ◽  
pp. 2591-2606 ◽  
Author(s):  
Lynn M. Russell ◽  
Kevin J. Noone ◽  
Ronald J. Ferek ◽  
Robert A. Pockalny ◽  
Richard C. Flagan ◽  
...  
Keyword(s):  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Condensation Nuclei ◽  
Ship Tracks
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