The underappreciated role of nonvolatile cations in aerosol ammonium-sulfate molar ratios

Overprediction of fine-particle ammonium-sulfate molar ratios (R) by thermodynamic models is suggested as evidence for interactions with organic constituents that inhibit the equilibration of gas-phase ammonia with aerosol sulfate and questions the equilibrium assumption long thought to apply for submicron aerosol. This hypothesis is tested through thermodynamic analysis of ambient observations. We find that the deviation between R from a molar ratio of 2 is strongly correlated with the concentration of sodium (Na+), a nonvolatile cation (NVC), but exhibits no correlation to organic aerosol (OA) mass concentration or mass fraction. Thermodynamic predictions of both R and ammonia gas–particle partitioning can accurately reproduce observations when small amounts of NVCs are included in the calculations, whereas exclusion of NVCs results in a predicted R consistently near 2. The sensitivity of R to small amounts of NVCs arises because, when the latter are present but not included in the thermodynamic calculations, the missing cations are replaced with ammonium in the model (NH3–NH4+ equilibrium shifts to the particle), resulting in an R that is biased high. Results and conclusions based on bulk aerosol considerations that assume all species are internally mixed are not changed even if NVCs and sulfate are largely externally mixed; fine-particle pH is found to be much less sensitive to mixing state assumptions than molar ratios. We also show that the data used to support the organic inhibition of NH3 from equilibrium, when compared against other network and field campaign datasets, display a systematically and significantly lower NH4+ (thought to be from an evaporation bias), that is of the order of the effect postulated to be caused by organics. Altogether, these results question the postulated ability of organic compounds to considerably perturb aerosol acidity and prevent ammonia from achieving gas–particle equilibrium, at least for the locations considered. Furthermore, the results demonstrate the limitations of using molar ratios to infer aerosol properties or processes that depend on particle pH.</p

Parameterizing the competition between homogeneous and heterogeneous freezing in cirrus cloud formation – monodisperse ice nuclei

We present a parameterization of cirrus cloud formation that computes the ice crystal number and size distribution under the presence of homogeneous and heterogeneous freezing. The parameterization is very simple to apply and is derived from the analytical solution of the cloud parcel equations, assuming that the ice nuclei population is monodisperse and chemically homogeneous. In addition to the ice distribution, an analytical expression is provided for the limiting ice nuclei number concentration that suppresses ice formation from homogeneous freezing. The parameterization is evaluated against a detailed numerical parcel model, and reproduces numerical simulations over a wide range of conditions with an average error of 6&amp;plusmn;33%. The parameterization also compares favorably against other formulations that require some form of numerical integration

Parameterizing the competition between homogeneous and heterogeneous freezing in ice cloud formation &ndash; polydisperse ice nuclei

This study presents a comprehensive ice cloud formation parameterization that computes the ice crystal number, size distribution, and maximum supersaturation from precursor aerosol and ice nuclei. The parameterization provides an analytical solution of the cloud parcel model equations and accounts for the competition effects between homogeneous and heterogeneous freezing, and, between heterogeneous freezing in different modes. The diversity of heterogeneous nuclei is described through a nucleation spectrum function which is allowed to follow any form (i.e., derived from classical nucleation theory or from observations). The parameterization reproduces the predictions of a detailed numerical parcel model over a wide range of conditions, and several expressions for the nucleation spectrum. The average error in ice crystal number concentration was &minus;2.0&plusmn;8.5% for conditions of pure heterogeneous freezing, and, 4.7&plusmn;21% when both homogeneous and heterogeneous freezing were active. The formulation presented is fast and free from requirements of numerical integration

Dynamical States of Low Temperature Cirrus

Low ice crystal concentration and sustained in-cloud supersaturation, commonly found in cloud observations at low temperature, challenge our understanding of cirrus formation. Heterogeneous freezing from effloresced ammonium sulfate, glassy aerosol, dust and black carbon are proposed to cause these phenomena; this requires low updrafts for cirrus characteristics to agree with observations and is at odds with the gravity wave spectrum in the upper troposphere. Background temperature fluctuations however can establish a dynamical equilibrium between ice production and sedimentation loss (as opposed to ice crystal formation during the first stages of cloud evolution and subsequent slow cloud decay) that explains low temperature cirrus properties. This newly-discovered state is favored at low temperatures and does not require heterogeneous nucleation to occur (the presence of ice nuclei can however facilitate its onset). Our understanding of cirrus clouds and their role in anthropogenic climate change is reshaped, as the type of dynamical forcing will set these clouds in one of two preferred microphysical regimes with very different susceptibility to aerosol

Water-soluble SOA from Alkene ozonolysis: composition and droplet activation kinetics inferences from analysis of CCN activity

Cloud formation characteristics of the water-soluble organic fraction (WSOC) of secondary organic aerosol (SOA) formed from the ozonolysis of alkene hydrocarbons (terpinolene, 1-methlycycloheptene and cycloheptene) are studied. Based on size-resolved measurements of CCN activity (of the pure and salted WSOC samples) we estimate the average molar volume and surface tension depression associated with the WSOC using Köhler Theory Analysis (KTA). Consistent with known speciation, the results suggest that the WSOC are composed of low molecular weight species, with an effective molar mass below 200 g mol^(−1). The water-soluble carbon is also surface-active, depressing surface tension 10–15% from that of pure water (at CCN-relevant concentrations). The inherent hygroscopicity parameter, κ, of the WSOC ranges between 0.17 and 0.25; if surface tension depression and molar volume effects are considered in κ, a remarkably constant "apparent" hygroscopicity ~0.3 emerges for all samples considered. This implies that the volume fraction of soluble material in the parent aerosol is the key composition parameter required for prediction of the SOA hygroscopicity, as shifts in molar volume across samples are compensated by changes in surface tension. Finally, using "threshold droplet growth analysis", the water-soluble organics in all samples considered do not affect CCN activation kinetics

Cloud droplet activation: solubility revisited

International audienceSoluble compounds present in atmospheric aerosol facilitate their transformation into cloud droplets by depressing the equilibrium vapor pressure required for activation. Their impact depends on the amount of dissolved substance in the aerosol aqueous phase, which in turn is controlled by its solubility. This study explores the impact of particle curvature on solubility, expressed in terms of a Kelvin enhancement. The augmented solubility, termed "Curvature Enhanced Solubility" (CES), is then introduced into Köhler theory for assessment of its impact on CCN activity for several organic compounds with a wide range of aqueous solubility. The interfacial energy between solute and aqueous phase required for quantification of CES is determined from existing correlations based on bulk solubility, and concurrent measurements of contact angle and surface tension. A number of important findings arise from this study: i) CES can substantially increase solubility and impact CCN activity but only if the aerosol is initially wet, ii) CES can stabilize highly supersaturated solutions, and provide a mechanism for retention of an aerosol aqueous phase even at very low relative humidity (RH), and, iii) trace amounts of surfactant impurities can magnify the impact of CES

Effectiveness of ammonia reduction on control of fine particle nitrate

In some regions, reducing aerosol ammonium nitrate (NH4NO3) concentrations may substantially improve air quality. This can be accomplished by reductions in precursor emissions, such as nitrogen oxides (NOx) to lower nitric acid (HNO3) that partitions to the aerosol, or reductions in ammonia (NH3) to lower particle pH and keep HNO3 in the gas phase. Using the ISORROPIA-II thermodynamic aerosol model and detailed observational data sets, we explore the sensitivity of aerosol NH4NO3 to gas-phase NH3 and NOx controls for a number of contrasting locations, including Europe, the United States, and China. NOx control is always effective, whereas the aerosol response to NH3 control is highly nonlinear and only becomes effective at a thermodynamic sweet spot. The analysis provides a conceptual framework and fundamental evaluation on the relative value of NOx versus NH3 control and demonstrates the relevance of pH as an air quality parameter. We find that, regardless of the locations examined, it is only when ambient particle pH drops below an approximate critical value of 3 (slightly higher in warm and slightly lower in cold seasons) that NH3 reduction leads to an effective response in PM2.5 mass. The required amount of NH3 reduction to reach the critical pH and efficiently decrease NH4NO3 at different sites is assessed. Owing to the linkage between NH3 emissions and agricultural productivity, the substantial NH3 reduction required in some locations may not be feasible. Finally, controlling NH3 emissions to increase aerosol acidity and evaporate NH4NO3 will have other effects, beyond reduction of PM2.5 NH4NO3, such as increasing aerosol toxicity and potentially altering the deposition patterns of nitrogen and trace nutrients.</p

How quickly do cloud droplets form on atmospheric particles?

International audienceThe influence of aerosols on cloud properties is an important modulator of the climate system. Traditional Köhler theory predicts the equilibrium concentration of cloud condensation nuclei (CCN); however, it is not known to what extent particles exist in the atmosphere that may be prevented from acting as CCN by kinetic limitations. We measured the rate of cloud droplet formation on atmospheric particles sampled at four sites across the United States during the summer of 2006: Great Smoky Mountain National Park, TN; Bondville, IL; Houston, TX; and the Atmospheric Radiation Measurement Program Southern Great Plains site near Lamont, OK. We express droplet growth rates with the mass accommodation coefficient (?), and report values of ? measured in the field normalized to the mean ? measured for lab-generated ammonium sulfate (AS) particles (i.e., ?'=?/?AS). Overall, 61% of ambient CCN grew at a rate similar to AS. We report the fraction of CCN that were "low-?'" (?'?0.33). Of the 16 days during which these measurements were made, 7 had relatively few low-?'CCN (77% during at least one ~30 min period). Day to day variability was greatest in Tennessee and Illinois, and low-?' CCN were most prevalent on days when back trajectories suggested that air was arriving from aloft. The highest fractions of low-?' CCN in Houston and Illinois occurred around local noon, and decreased later in the day. These results suggest that for some air masses, accurate quantification of CCN concentrations may need to account for kinetic limitations

Adjoint sensitivity of global cloud droplet number to aerosol and dynamical parameters

We present the development of the adjoint of a comprehensive cloud droplet formation parameterization for use in aerosol-cloud-climate interaction studies. The adjoint efficiently and accurately calculates the sensitivity of cloud droplet number concentration (CDNC) to all parameterization inputs (e.g., updraft velocity, water uptake coefficient, aerosol number and hygroscopicity) with a single execution. The adjoint is then integrated within three dimensional (3-D) aerosol modeling frameworks to quantify the sensitivity of CDNC formation globally to each parameter. Sensitivities are computed for year-long executions of the NASA Global Modeling Initiative (GMI) Chemical Transport Model (CTM), using wind fields computed with the Goddard Institute for Space Studies (GISS) Global Circulation Model (GCM) II', and the GEOS-Chem CTM, driven by meteorological input from the Goddard Earth Observing System (GEOS) of the NASA Global Modeling and Assimilation Office (GMAO). We find that over polluted (pristine) areas, CDNC is more sensitive to updraft velocity and uptake coefficient (aerosol number and hygroscopicity). Over the oceans of the Northern Hemisphere, addition of anthropogenic or biomass burning aerosol is predicted to increase CDNC in contrast to coarse-mode sea salt which tends to decrease CDNC. Over the Southern Oceans, CDNC is most sensitive to sea salt, which is the main aerosol component of the region. Globally, CDNC is predicted to be less sensitive to changes in the hygroscopicity of the aerosols than in their concentration with the exception of dust where CDNC is very sensitive to particle hydrophilicity over arid areas. Regionally, the sensitivities differ considerably between the two frameworks and quantitatively reveal why the models differ considerably in their indirect forcing estimates

CCN activity and droplet growth kinetics of fresh and aged monoterpene secondary organic aerosol

International audienceThe ability of secondary organic aerosol (SOA) produced from the ozonolysis of ?-pinene and monoterpene mixtures (?-pinene, ?-pinene, limonene and 3-carene) to become cloud droplets was investigated. Monoterpene SOA is quite active and would likely be a good source of cloud condensation nuclei (CCN) in the atmosphere. A static CCN counter and a Scanning Mobility CCN Analyser (a Scanning Mobility Particle Sizer coupled with a Continuous Flow counter) were used for the CCN measurements. A decrease in CCN activation diameter for ?-pinene SOA of approximately 3 nm h?1 was observed as the aerosol continued to react with oxidants. Hydroxyl radicals further oxidize the SOA particles thereby enhancing the particle CCN activity with time. The initial concentrations of ozone and monoterpene precursor (for concentrations lower than 40 ppb) do not appear to affect the activity of the resulting SOA. Köhler Theory Analysis (KTA) is used to infer the molar mass of the SOA sampled online and offline from atomized filter samples. KTA suggests that the aged aerosol (both from ?-pinene and the mixed monoterpene oxidation) is primarily water-soluble (around 70?80%), with an estimated average molar mass of 180±55 g mol?1 (consistent with existing SOA speciation studies). CCN activity measurements of the SOA mixed with (NH4)2SO4 suggest that the organic can depress surface tension by as much as 10 nM m?1 (with respect to pure water). The droplet growth kinetics of SOA samples are similar to (NH4)2SO4, except at low supersaturation, where SOA tends to grow more slowly. The CCN activity of ?-pinene and mixed monoterpene SOA can be modelled by a very simple implementation of Köhler theory, assuming complete dissolution of the particles, no dissociation into ions, molecular weight of 180 g mol?1, density of 1.5 g cm?3, and surface tension to within 10?15% of water