scholarly journals Effect of primary organic sea spray emissions on cloud condensation nuclei concentrations

2012 ◽  
Vol 12 (1) ◽  
pp. 89-101 ◽  
Author(s):  
D. M. Westervelt ◽  
R. H. Moore ◽  
A. Nenes ◽  
P. J. Adams
Keyword(s):  
Surface Tension ◽  
Southern Ocean ◽  
Source Function ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Sea Salt ◽  
Sea Spray ◽  
Aerosol Emission ◽  
Sea Spray Aerosol ◽  
Surfactant Effects

Abstract. This work estimates the primary marine organic aerosol global emission source and its impact on cloud condensation nuclei (CCN) concentrations by implementing an organic sea spray source function into a series of global aerosol simulations. The source function assumes that a fraction of the sea spray emissions, depending on the local chlorophyll concentration, is organic matter in place of sea salt. Effect on CCN concentrations (at 0.2% supersaturation) is modeled using the Two-Moment Aerosol Sectional (TOMAS) microphysics algorithm coupled to the GISS II-prime general circulation model. The presence of organics affects CCN activity in competing ways: by reducing the amount of solute available in the particle and decreasing surface tension of CCN. To model surfactant effects, surface tension depression data from seawater samples taken near the Georgia coast were applied as a function of carbon concentrations. A global marine organic aerosol emission rate of 17.7 Tg C yr−1 is estimated from the simulations. Marine organics exert a localized influence on CCN(0.2%) concentrations, decreasing regional concentrations by no more than 5% and by less than 0.5% over most of the globe, assuming direct replacement of sea salt aerosol with organic aerosol. The decrease in CCN concentrations results from the fact that the decrease in particle solute concentration outweighs the organic surfactant effects. The low sensitivity of CCN(0.2%) to the marine organic emissions is likely due to the small compositional changes: the mass fraction of OA in accumulation mode aerosol increases by only ~15% in a biologically active region of the Southern Ocean. To test the sensitivity to uncertainty in the sea spray emissions process, we relax the assumption that sea spray aerosol number and mass remain fixed and instead can add to sea spray emissions rather than replace existing sea salt. In these simulations, we find that marine organic aerosol can increase CCN by up to 50% in the Southern Ocean and 3.7% globally during the austral summer. This vast difference in CCN impact highlights the need for further observational exploration of the sea spray aerosol emission process as well as evaluation and development of model parameterizations.

scholarly journals Effect of primary organic sea spray emissions on cloud condensation nuclei concentrations

2011 ◽  
Vol 11 (2) ◽  
pp. 5757-5784 ◽  
Author(s):  
D. M. Westervelt ◽  
R. H. Moore ◽  
A. Nenes ◽  
P. J. Adams
Keyword(s):  
Surface Tension ◽  
General Circulation ◽  
Source Function ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Biologically Active ◽  
Sea Spray ◽  
Condensation Nuclei ◽  
Aerosol Emission ◽  
Surfactant Effects

Abstract. This work quantifies the primary marine organic aerosol global emission source and its impact on cloud condensation nuclei (CCN) concentrations by implementing an organic sea spray source function into a series of global aerosol simulations. The source function assumes that a fraction of the sea spray emissions, depending on the local chlorophyll concentration, is organic matter in place of NaCl. Effect on CCN concentrations (at 0.2% supersaturation) is modeled using the Two-Moment Aerosol Sectional (TOMAS) microphysics algorithm coupled to the GISS II-prime general circulation model. The presence of organics affects CCN activity in competing ways: by reducing the amount of solute available in the particle and decreasing surface tension of CCN. To model surfactant effects, surface tension depression data from seawater samples taken near the Georgia coast were applied as a function of carbon concentrations. A global marine organic aerosol emission rate of 17.7 Tg C yr−1 is estimated from the simulations. Marine organics exert a localized influence on CCN(0.2%) concentrations, decreasing regional concentrations by no more than 5% and by less than 0.5% over most of the globe. The decrease in CCN concentrations results from the fact that the decrease in particle solute concentration outweighs the organic surfactant effects. The low sensitivity of CCN(0.2%) to the marine organic emissions is likely due to the small compositional changes: the mass fraction of OA in accumulation mode aerosol increases by only 15% in a biologically active region of the Southern Ocean.

The sensitivity of Southern Ocean aerosol concentrations to sea spray and DMS emissions in the HadGEM3-GA7.1 chemistry–climate model

2020 ◽  
Author(s):  
Laura Revell ◽  
Stefanie Kremser ◽  
Sean Hartery ◽  
Mike Harvey ◽  
Jane Mulcahy ◽  
...  
Keyword(s):  
Wind Speed ◽  
Southern Ocean ◽  
Source Function ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Number Concentration ◽  
Sea Spray ◽  
Condensation Nuclei ◽  
Sea Spray Aerosol ◽  
Aerosol Source

<p>With low concentrations of tropospheric aerosol, the Southern Ocean offers a "natural laboratory" for studies of aerosol–cloud interactions. Aerosols over the Southern Ocean are produced from biogenic activity in the ocean, which generates sulfate aerosol via dimethylsulfide (DMS) oxidation, and from strong winds and waves that lead to bubble bursting and sea spray emission. Here, we evaluate the representation of Southern Ocean aerosols in the Hadley Centre Global Environmental Model version 3, Global Atmosphere 7.1 (HadGEM3-GA7.1) chemistry–climate model. Compared with aerosol optical depth (AOD) observations from two satellite instruments (the Moderate Resolution Imaging Spectroradiometer, MODIS-Aqua c6.1, and the Multi-angle Imaging Spectroradiometer, MISR), the model simulates too-high AOD during winter and too-low AOD during summer. By switching off DMS emission in the model, we show that sea spray aerosol is the dominant contributor to AOD during winter. In turn, the simulated sea spray aerosol flux depends on near-surface wind speed. By examining MODIS AOD as a function of wind speed from the ERA-Interim reanalysis and comparing it with the model, we show that the sea spray aerosol source function in HadGEM3-GA7.1 overestimates the wind speed dependency. We test a recently developed sea spray aerosol source function derived from measurements made on a Southern Ocean research voyage in 2018. In this source function, the wind speed dependency of the sea spray aerosol flux is less than in the formulation currently implemented in HadGEM3-GA7.1. The new source function leads to good agreement between simulated and observed wintertime AODs over the Southern Ocean; however, it reveals partially compensating errors in DMS-derived AOD. While previous work has tested assumptions regarding the seawater climatology or sea–air flux of DMS, we test the sensitivity of simulated AOD, cloud condensation nuclei and cloud droplet number concentration to three atmospheric sulfate chemistry schemes. The first scheme adds DMS oxidation by halogens and the other two test a recently developed sulfate chemistry scheme for the marine troposphere; one tests gas-phase chemistry only, while the second adds extra aqueous-phase sulfate reactions. We show how simulated sulfur dioxide and sulfuric acid profiles over the Southern Ocean change as a result and how the number concentration and particle size of the soluble Aitken, accumulation and coarse aerosol modes are affected. The new DMS chemistry scheme leads to a 20% increase in the number concentration of cloud condensation nuclei and cloud droplets, which improves agreement with observations. Our results highlight the importance of atmospheric chemistry for simulating aerosols and clouds accurately over the Southern Ocean.</p>

scholarly journals The sensitivity of Southern Ocean aerosols and cloud microphysics to sea spray and sulfate aerosol production in the HadGEM3-GA7.1 chemistry-climate model

2019 ◽  
Author(s):  
Laura E. Revell ◽  
Stefanie Kremser ◽  
Sean Hartery ◽  
Mike Harvey ◽  
Jane P. Mulcahy ◽  
...  
Keyword(s):  
Wind Speed ◽  
Southern Ocean ◽  
Source Function ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Number Concentration ◽  
Sea Spray ◽  
Condensation Nuclei ◽  
Sea Spray Aerosol ◽  
Aerosol Source

Abstract. With low concentrations of tropospheric aerosol, the Southern Ocean offers a natural laboratory for studies of aerosol-cloud interactions. Aerosols over the Southern Ocean are produced from biogenic activity in the ocean, which generates sulfate aerosol via dimethylsulfide (DMS) oxidation, and from strong winds and waves that lead to bubble bursting and sea-spray emission. Here we evaluate the representation of Southern Ocean aerosols in the HadGEM3-GA7.1 chemistry-climate model. Compared with aerosol optical depth (AOD) observations from two satellite instruments (the Moderate Resolution Imaging Spectroradiometer, MODIS-Aqua c6.1 and the Multi-angle Imaging Spectroradiometer, MISR), the model simulates too-high AOD during winter and too-low AOD during summer. By switching off DMS emission in the model, we show that sea spray aerosol is the dominant contributor to AOD during winter. In turn, the simulated sea spray aerosol flux depends on near-surface wind speed. By examining MODIS AOD as a function of wind speed from the ERA-Interim reanalysis and comparing it with the model, we show that the sea spray aerosol source function in HadGEM3-GA7.1 overestimates the wind speed dependency. We test a recently-developed sea spray aerosol source function derived from measurements made on a Southern Ocean research voyage in 2018. In this source function the wind speed dependency of the sea spray aerosol flux is less than in the formulation currently implemented in HadGEM3-GA7.1. The new source function leads to good agreement between simulated and observed wintertime AOD over the Southern Ocean, however reveals partially compensating errors in DMS-derived AOD. While previous work has tested assumptions regarding the seawater climatology or sea-air flux of DMS, we test the sensitivity of simulated AOD, cloud condensation nuclei and cloud droplet number concentration to three atmospheric sulfate chemistry schemes. The first scheme adds DMS oxidation by halogens and the other two test a recently-developed sulfate chemistry scheme for the marine troposphere; one tests gas-phase chemistry only while the second adds extra aqueous-phase sulfate reactions. We show how simulated sulfur dioxide and sulfuric acid profiles over the Southern Ocean change as a result, and how the number concentration and particle size of the soluble Aitken, accumulation and coarse aerosol modes are affected. The new DMS chemistry scheme leads to a 20 % increase in the number concentration of cloud condensation nuclei and cloud droplets, which improves agreement with observations. Our results highlight the importance of atmospheric chemistry for simulating aerosols and clouds accurately over the Southern Ocean.

scholarly journals OCEANFILMS sea-spray organic aerosol emissions – Part 1: implementation and impacts on clouds

2018 ◽  
Author(s):  
Susannah M. Burrows ◽  
Richard Easter ◽  
Xiaohong Liu ◽  
Po-Lun Ma ◽  
Hailong Wang ◽  
...  
Keyword(s):  
Southern Ocean ◽  
Radiative Forcing ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Earth System Model ◽  
Sea Salt ◽  
System Model ◽  
Sea Spray ◽  
Earth System ◽  
Aerosol Emissions

Abstract. The OCEANFILMS parameterization for sea-spray organic aerosol emissions has been implemented into a global Earth system model, the Energy Exascale Earth System Model (E3SM). OCEANFILMS is a physically-based model that links sea spray chemistry with ocean biogeochemistry using a Langmuir partitioning approach. Here we describe the implementation within E3SM and investigate the impacts of the parameterization on the model's aerosols, clouds and climate. Four sensitivity cases are tested, in which organic emissions either strictly add to or strictly replace sea salt emissions (in mass and number), and are either fully internally or fully externally mixed with sea salt. The simulation with internally-mixed, added organics agrees best with observed seasonal cycles of organic matter in marine aerosol. In this configuration, marine organic aerosols contribute an additional source of cloud condensation nuclei, adding up to 30 cm−3 to Southern Ocean boundary-layer CCN concentrations (supersaturation = 0.1 %). The addition of this new aerosol source strengthens shortwave radiative cooling by clouds by −0.36 W/m2 in the global annual mean, and contributes more than −3.5 W/m2 to summertime zonal mean cloud forcing in the Southern Ocean, with maximum zonal mean impacts of about −4 W/m2 around 50° S–60° S. This is consistent with a previous top-down, satellite-based empirical estimate of the radiative forcing by marine organic aerosol over the Southern Ocean.

scholarly journals The sensitivity of Southern Ocean aerosols and cloud microphysics to sea spray and sulfate aerosol production in the HadGEM3-GA7.1 chemistry–climate model

2019 ◽  
Vol 19 (24) ◽  
pp. 15447-15466 ◽  
Author(s):  
Laura E. Revell ◽  
Stefanie Kremser ◽  
Sean Hartery ◽  
Mike Harvey ◽  
Jane P. Mulcahy ◽  
...  
Keyword(s):  
Wind Speed ◽  
Southern Ocean ◽  
Source Function ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Number Concentration ◽  
Sea Spray ◽  
Condensation Nuclei ◽  
Sea Spray Aerosol ◽  
Aerosol Source

Abstract. With low concentrations of tropospheric aerosol, the Southern Ocean offers a “natural laboratory” for studies of aerosol–cloud interactions. Aerosols over the Southern Ocean are produced from biogenic activity in the ocean, which generates sulfate aerosol via dimethylsulfide (DMS) oxidation, and from strong winds and waves that lead to bubble bursting and sea spray emission. Here, we evaluate the representation of Southern Ocean aerosols in the Hadley Centre Global Environmental Model version 3, Global Atmosphere 7.1 (HadGEM3-GA7.1) chemistry–climate model. Compared with aerosol optical depth (AOD) observations from two satellite instruments (the Moderate Resolution Imaging Spectroradiometer, MODIS-Aqua c6.1, and the Multi-angle Imaging Spectroradiometer, MISR), the model simulates too-high AOD during winter and too-low AOD during summer. By switching off DMS emission in the model, we show that sea spray aerosol is the dominant contributor to AOD during winter. In turn, the simulated sea spray aerosol flux depends on near-surface wind speed. By examining MODIS AOD as a function of wind speed from the ERA-Interim reanalysis and comparing it with the model, we show that the sea spray aerosol source function in HadGEM3-GA7.1 overestimates the wind speed dependency. We test a recently developed sea spray aerosol source function derived from measurements made on a Southern Ocean research voyage in 2018. In this source function, the wind speed dependency of the sea spray aerosol flux is less than in the formulation currently implemented in HadGEM3-GA7.1. The new source function leads to good agreement between simulated and observed wintertime AODs over the Southern Ocean; however, it reveals partially compensating errors in DMS-derived AOD. While previous work has tested assumptions regarding the seawater climatology or sea–air flux of DMS, we test the sensitivity of simulated AOD, cloud condensation nuclei and cloud droplet number concentration to three atmospheric sulfate chemistry schemes. The first scheme adds DMS oxidation by halogens and the other two test a recently developed sulfate chemistry scheme for the marine troposphere; one tests gas-phase chemistry only, while the second adds extra aqueous-phase sulfate reactions. We show how simulated sulfur dioxide and sulfuric acid profiles over the Southern Ocean change as a result and how the number concentration and particle size of the soluble Aitken, accumulation and coarse aerosol modes are affected. The new DMS chemistry scheme leads to a 20 % increase in the number concentration of cloud condensation nuclei and cloud droplets, which improves agreement with observations. Our results highlight the importance of atmospheric chemistry for simulating aerosols and clouds accurately over the Southern Ocean.

scholarly journals Model evaluation of marine primary organic aerosol emission schemes

2012 ◽  
Vol 12 (18) ◽  
pp. 8553-8566 ◽  
Author(s):  
B. Gantt ◽  
M. S. Johnson ◽  
N. Meskhidze ◽  
J. Sciare ◽  
J. Ovadnevaite ◽  
...  
Keyword(s):  
Model Comparison ◽  
Transport Model ◽  
Organic Aerosol ◽  
Sea Spray ◽  
Mean Values ◽  
Chl A ◽  
Aerosol Mass ◽  
Aerosol Mass Concentration ◽  
Aerosol Emission ◽  
Sea Spray Aerosol

Abstract. In this study, several marine primary organic aerosol (POA) emission schemes have been evaluated using the GEOS-Chem chemical transport model in order to provide guidance for their implementation in air quality and climate models. These emission schemes, based on varying dependencies of chlorophyll a concentration ([chl a]) and 10 m wind speed (U10), have large differences in their magnitude, spatial distribution, and seasonality. Model comparison with weekly and monthly mean values of the organic aerosol mass concentration at two coastal sites shows that the source function exclusively related to [chl a] does a better job replicating surface observations. Sensitivity simulations in which the negative U10 and positive [chl a] dependence of the organic mass fraction of sea spray aerosol are enhanced show improved prediction of the seasonality of the marine POA concentrations. A top-down estimate of submicron marine POA emissions based on the parameterization that compares best to the observed weekly and monthly mean values of marine organic aerosol surface concentrations has a global average emission rate of 6.3 Tg yr−1. Evaluation of existing marine POA source functions against a case study during which marine POA contributed the major fraction of submicron aerosol mass shows that none of the existing parameterizations are able to reproduce the hourly-averaged observations. Our calculations suggest that in order to capture episodic events and short-term variability in submicron marine POA concentration over the ocean, new source functions need to be developed that are grounded in the physical processes unique to the organic fraction of sea spray aerosol.

scholarly journals The physical and chemical characteristics of marine organic aerosols: a review

2012 ◽  
Vol 12 (8) ◽  
pp. 21779-21813 ◽  
Author(s):  
B. Gantt ◽  
N. Meskhidze
Keyword(s):  
Chemical Composition ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosols ◽  
Organic Aerosol ◽  
Sea Salt ◽  
Sea Spray ◽  
Mixing State ◽  
Climatic Impact ◽  
Anthropogenic Aerosol

Abstract. Knowledge of the physical characteristics and chemical composition of marine organic aerosols is needed for the quantification of their effects on solar radiation transfer and cloud processes. Global emission estimates of marine organic aerosol are in a range of 2 to 70 Tg yr−1 and occur over regions most susceptible to aerosol perturbations. This review examines research pertinent to the chemical composition, size distribution, mixing state, emission mechanism, and climatic impact of marine primary organic aerosols associated with sea spray. Numerous measurements have shown that both the ambient mass concentration of marine organic aerosol and size-resolved organic mass fraction of sea spray aerosol are related to surface ocean biological activity. Recent studies have also indicated that fine mode (smaller than 200 nm in diameter) marine organic aerosols can have a size distribution independent from sea-salt, while coarse mode aerosols (larger than 1000 nm in diameter) are more likely to be internally-mixed with sea-salt. Climate studies have found that marine organic aerosols can cause large local increases in the cloud condensation nuclei concentration, with the potential to have a non-negligible influence on the anthropogenic aerosol indirect forcing. Despite these signs of climate-relevance for marine organic aerosols, the source strength, chemical composition, mixing state, hygroscopicity, cloud droplet activation potential, atmospheric aging, and removal of marine organic aerosols remain poorly quantified. Additional laboratory, field, and modeling studies focused on the chemistry, size distribution, and mixing state of sea spray aerosols are needed to better understand and quantify their importance.

scholarly journals Model evaluation of marine primary organic aerosol emission schemes

2012 ◽  
Vol 12 (5) ◽  
pp. 12853-12883 ◽  
Author(s):  
B. Gantt ◽  
M. S. Johnson ◽  
N. Meskhidze ◽  
J. Sciare ◽  
J. Ovadnevaite ◽  
...  
Keyword(s):  
Model Comparison ◽  
Transport Model ◽  
Organic Aerosol ◽  
Sea Spray ◽  
Mean Values ◽  
Chl A ◽  
Aerosol Mass ◽  
Aerosol Mass Concentration ◽  
Aerosol Emission ◽  
Sea Spray Aerosol

Abstract. In this study, five different marine primary organic aerosol (POA) emission schemes have been evaluated using the GEOS-Chem chemical transport model in order to provide guidance for their implementation in air quality and climate models. These emission schemes, categorized in two groups based on varying dependences of chlorophyll a concentration ([chl a]) and 10 m wind speed (U10), have large differences in their magnitude, spatial distribution, and seasonality. Model comparison with weekly and monthly mean values of the organic aerosol mass concentration at two coastal sites shows that the source function exclusively related to [chl a] does a better job replicating surface observations. Sensitivity simulations of the sea spray-based parameterizations show that improved predictions of the seasonality of the marine POA concentrations can be achieved by varying the U10 and [chl a] dependence of the organic mass fraction of sea spray aerosol. A top-down estimate of submicron marine POA emissions based on the parameterization that compares best to the observed weekly and monthly mean values of marine organic aerosol surface concentrations has a global average emission rate of 6.3 Tg yr−1. Evaluation of existing marine POA source functions against a case study during which marine POA contributed the major fraction of submicron aerosol mass shows that none of the existing parameterizations are able to reproduce the hourly-averaged observations. Our calculations suggest that in order to capture episodic events in submicron marine POA concentration over the ocean, new source functions need to be developed that are grounded in the physical processes unique to the organic fraction of sea spray aerosol.

scholarly journals The physical and chemical characteristics of marine primary organic aerosol: a review

2013 ◽  
Vol 13 (8) ◽  
pp. 3979-3996 ◽  
Author(s):  
B. Gantt ◽  
N. Meskhidze
Keyword(s):  
Chemical Composition ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Organic Aerosol ◽  
Sea Salt ◽  
Photochemical Oxidation ◽  
Sea Spray ◽  
Mixing State ◽  
Anthropogenic Aerosol ◽  
Modelling Studies

Abstract. Knowledge of the physical characteristics and chemical composition of marine organic aerosols is needed for the quantification of their effects on solar radiation transfer and cloud processes. This review examines research pertinent to the chemical composition, size distribution, mixing state, emission mechanism, photochemical oxidation and climatic impact of marine primary organic aerosol (POA) associated with sea-spray. Numerous measurements have shown that both the ambient mass concentration of marine POA and size-resolved organic mass fraction of sea-spray aerosol are related to surface ocean biological activity. Recent studies have also indicated that fine mode (smaller than 200 nm in diameter) marine POA can have a size distribution independent from sea-salt, while coarse mode aerosols (larger than 1000 nm in diameter) are more likely to be internally mixed with sea-salt. Modelling studies have estimated global submicron marine POA emission rates of ~10 ± 5 Tg yr−1, with a considerable fraction of these emissions occurring over regions most susceptible to aerosol perturbations. Climate studies have found that marine POA can cause large local increases in the cloud condensation nuclei concentration and have a non-negligible influence on model assessments of the anthropogenic aerosol forcing of climate. Despite these signs of climate-relevance, the source strength, chemical composition, mixing state, hygroscopicity, cloud droplet activation potential, atmospheric aging and removal of marine POA remain poorly quantified. Additional laboratory, field, and modelling studies focused on the chemistry, size distribution and mixing state of marine POA are needed to better understand and quantify their importance.

scholarly journals Linking variations in sea spray aerosol particle hygroscopicity to composition during two microcosm experiments

2016 ◽  
Author(s):  
Sara D. Forestieri ◽  
Gavin C. Cornwell ◽  
Taylor M. Helgestad ◽  
Kathryn A. Moore ◽  
Christopher Lee ◽  
...  
Keyword(s):  
Light Scattering ◽  
Relative Humidity ◽  
Salt Content ◽  
Sea Salt ◽  
Sea Spray ◽  
Hygroscopic Growth ◽  
Phytoplankton Blooms ◽  
Aerosol Composition ◽  
Sea Spray Aerosol ◽  
Indoor And Outdoor

Abstract. The extent to which water uptake influences the light scattering ability of marine sea spray aerosol (SSA) particles depends critically on SSA chemical composition. The organic fraction of SSA can increase during phytoplankton blooms, decreasing the salt content and therefore the hygroscopicity of the particles. In this study, subsaturated hygroscopic growth factors at 85 % relative humidity (GF(85 %)) of SSA particles were quantified during two induced phytoplankton blooms in marine aerosol reference tanks (MARTs). One MART was illuminated with fluorescent lights and the other was illuminated with sunlight, referred to as the "indoor" and "outdoor" MARTs, respectively. GF(85 %) values for SSA particles were derived from measurements of light scattering and particle size distributions, concurrently with online single particle and bulk aerosol composition measurements. During both microcosm experiments, the observed bulk average GF(85 %) values were depressed substantially relative to pure, inorganic sea salt, by 10 to 19 %, with a one (indoor MART) and six (outdoor MART) day lag between GF(85 %) depression and the peak chlorophyll-a concentrations. The fraction of organiccontaining SSA particles generally increased after the peak of the phytoplankton blooms. The GF(85 %) values were inversely correlated with the fraction of particles containing organic or other biological markers. This indicates these particles were less hygroscopic than the particles identified as predominately sea salt containing and demonstrates a clear relationship between SSA particle composition and the sensitivity of light scattering to variations in relative humidity. The implications of these observations to the direct climate effects of SSA particles are discussed.

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