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A two-dimensional volatility basis set: 1. organic-aerosol mixing thermodynamics
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Donahue N.M.; Epstein S.A.; Pandis S.N.; et al. - Copernicus GmbH, 2011We develop the thermodynamic underpinnings of a two-dimensional volatility basis set (2D-VBS) employing saturation mass concentration (Co) and the oxygen content (O:C) to describe volatility, mixing thermodynamics, and chemical evolution of organic aerosol. The work addresses a simple question: "Can we reasonably constrain organic-aerosol composition in the atmosphere based on only two measurable organic properties, volatility and the extent of oxygenation?" This is an extension of our earlier one-dimensional approach employing volatility only (C* = γ Co, where γ is an activity coefficient). U ...
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Available online: http://dx.doi.org/10.5194/acp-11-3303-2011
in Atmospheric Chemistry and Physics (ACP) > Vol. 11. N° 7 [04/01/2011] . - p.3303-3318We develop the thermodynamic underpinnings of a two-dimensional volatility basis set (2D-VBS) employing saturation mass concentration (Co) and the oxygen content (O:C) to describe volatility, mixing thermodynamics, and chemical evolution of organic aerosol. The work addresses a simple question: "Can we reasonably constrain organic-aerosol composition in the atmosphere based on only two measurable organic properties, volatility and the extent of oxygenation?" This is an extension of our earlier one-dimensional approach employing volatility only (C* = γ Co, where γ is an activity coefficient). Using available constraints on bulk organic-aerosol composition, we argue that one can reasonably predict the composition of organics (carbon, oxygen and hydrogen numbers) given a location in the Co – O:C space. Further, we argue that we can constrain the activity coefficients at various locations in this space based on the O:C of the organic aerosol.
Language(s): English
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On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Held A.; Brooks I.M.; Leck C.; et al. - Copernicus GmbH, 2011We present direct eddy covariance measurements of aerosol number fluxes, dominated by sub-50 nm particles, at the edge of an ice floe drifting in the central Arctic Ocean. The measurements were made during the ice-breaker borne ASCOS (Arctic Summer Cloud Ocean Study) expedition in August 2008 between 2°–10° W longitude and 87°–87.5° N latitude. The median aerosol transfer velocities over different surface types (open water leads, ice ridges, snow and ice surfaces) ranged from 0.27 to 0.68 mm s−1 during deposition-dominated episodes. Emission periods were observed more frequently over the open ...
[article]On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
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Available online: http://dx.doi.org/10.5194/acp-11-3093-2011
in Atmospheric Chemistry and Physics (ACP) > Vol. 11. N° 7 [04/01/2011] . - p.3093-3105We present direct eddy covariance measurements of aerosol number fluxes, dominated by sub-50 nm particles, at the edge of an ice floe drifting in the central Arctic Ocean. The measurements were made during the ice-breaker borne ASCOS (Arctic Summer Cloud Ocean Study) expedition in August 2008 between 2°–10° W longitude and 87°–87.5° N latitude. The median aerosol transfer velocities over different surface types (open water leads, ice ridges, snow and ice surfaces) ranged from 0.27 to 0.68 mm s−1 during deposition-dominated episodes. Emission periods were observed more frequently over the open lead, while the snow behaved primarily as a deposition surface. Directly measured aerosol fluxes were compared with particle deposition parameterizations in order to estimate the emission flux from the observed net aerosol flux. Finally, the contribution of the open lead particle source to atmospheric variations in particle number concentration was evaluated and compared with the observed temporal evolution of particle number. The direct emission of aerosol particles from the open lead can explain only 5–10% of the observed particle number variation in the mixing layer close to the surface.
Language(s): English
Format: Digital (Free)Tags: Aerosols ; Atmosphere ; Research ; Arctic
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Global distribution of sea salt aerosols: new constraints from in situ and remote sensing observations
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Jaeglé L.; Quinn P.K.; Bates T.S.; et al. - Copernicus GmbH, 2011We combine in situ measurements of sea salt aerosols (SS) from open ocean cruises and ground-based stations together with aerosol optical depth (AOD) observations from MODIS and AERONET, and the GEOS-Chem global chemical transport model to provide new constraints on SS emissions over the world's oceans. We find that the GEOS-Chem model using the Gong (2003) source function overestimates cruise observations of coarse mode SS mass concentrations by factors of 2–3 at high wind speeds over the cold waters of the Southern, North Pacific and North Atlantic Oceans. Furthermore, the model systematical ...
[article]Global distribution of sea salt aerosols: new constraints from in situ and remote sensing observations
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Available online: http://dx.doi.org/10.5194/acp-11-3137-2011
L. Jaeglé ; P.K. Quinn ; T.S. Bates ; B. Alexander ; J.-T. Lin
in Atmospheric Chemistry and Physics (ACP) > Vol. 11. N° 7 [04/01/2011] . - p.3137-3157We combine in situ measurements of sea salt aerosols (SS) from open ocean cruises and ground-based stations together with aerosol optical depth (AOD) observations from MODIS and AERONET, and the GEOS-Chem global chemical transport model to provide new constraints on SS emissions over the world's oceans. We find that the GEOS-Chem model using the Gong (2003) source function overestimates cruise observations of coarse mode SS mass concentrations by factors of 2–3 at high wind speeds over the cold waters of the Southern, North Pacific and North Atlantic Oceans. Furthermore, the model systematically underestimates SS over the warm tropical waters of the Central Pacific, Atlantic, and Indian Oceans. This pattern is confirmed by SS measurements from a global network of 15 island and coastal stations. The model discrepancy at high wind speeds (>6 m s −1) has a clear dependence on sea surface temperature (SST). We use the cruise observations to derive an empirical SS source function depending on both wind speed and SST. Implementing this new source function in GEOS-Chem results in improved agreement with in situ observations, with a decrease in the model bias from +64% to +33% for the cruises and from +32% to −5% for the ground-based sites. We also show that the wind speed-SST source function significantly improves agreement with MODIS and AERONET AOD, and provides an explanation for the high AOD observed over the tropical oceans. With the wind speed-SST formulation, global SS emissions show a small decrease from 5200 Mg yr−1 to 4600 Mg yr−1, while the SS burden decreases from 9.1 to 8.5 mg m−2. The spatial distribution of SS, however, is greatly affected, with the SS burden increasing by 50% in the tropics and decreasing by 40% at mid- and high-latitudes. Our results imply a stronger than expected halogen source from SS in the tropical marine boundary layer. They also imply stronger radiative forcing of SS in the tropics and a larger response of SS emissions to climate change than previously thought.
Language(s): English
Format: Digital (Free)Tags: Aerosols ; Methodology ; Observations
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The effect of meteorological and chemical factors on the agreement between observations and predictions of fine aerosol composition in southwestern Ontario during BAQS-Met
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Markovic M.Z.; Hayden K.L.; Murphy J.G.; et al. - Copernicus GmbH, 2011The Border Air Quality and Meteorology Study (BAQS-Met) was an intensive, collaborative field campaign during the summer of 2007 that investigated the effects of transboundary pollution, local pollution, and local meteorology on air quality in southwestern Ontario. This analysis focuses on the measurements of the inorganic constituents of particulate matter with diameter of less than 1 μm (PM1), with a specific emphasis on nitrate. We evaluate the ability of AURAMS, Environment Canada's chemical transport model, to represent regional air pollution in SW Ontario by comparing modelled aerosol in ...
[article]The effect of meteorological and chemical factors on the agreement between observations and predictions of fine aerosol composition in southwestern Ontario during BAQS-Met
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Available online: http://dx.doi.org/10.5194/acp-11-3195-2011
M.Z. Markovic ; K.L. Hayden ; J.G. Murphy ; P.A. Makar ; R.A. Ellis ; R.Y.-W. Chang ; J.G. Slowik ; C. Mihele ; J. Brook
in Atmospheric Chemistry and Physics (ACP) > Vol. 11. N° 7 [04/01/2011] . - p.3195-3210The Border Air Quality and Meteorology Study (BAQS-Met) was an intensive, collaborative field campaign during the summer of 2007 that investigated the effects of transboundary pollution, local pollution, and local meteorology on air quality in southwestern Ontario. This analysis focuses on the measurements of the inorganic constituents of particulate matter with diameter of less than 1 μm (PM1), with a specific emphasis on nitrate. We evaluate the ability of AURAMS, Environment Canada's chemical transport model, to represent regional air pollution in SW Ontario by comparing modelled aerosol inorganic chemical composition with measurements from Aerosol Mass Spectrometers (AMS) onboard the National Research Council (NRC) of Canada Twin Otter aircraft and at a ground site in Harrow, ON. The agreement between modelled and measured pNO3− at the ground site (observed mean (Mobs) = 0.50 μg m−3; modelled mean (Mmod) = 0.58 μg m−3; root mean square error (RSME) = 1.27 μg m−3) was better than aloft (Mobs = 0.32 μg m−3; Mmod = 0.09 μg m−3; RSME = 0.48 μg m−3). Possible reasons for discrepancies include errors in (i) emission inventories, (ii) atmospheric chemistry, (iii) predicted meteorological parameters, or (iv) gas/particle thermodynamics in the model framework. Using the inorganic thermodynamics model, ISORROPIA, in an offline mode, we find that the assumption of thermodynamic equilibrium is consistent with observations of gas and particle composition at Harrow. We develop a framework to assess the sensitivity of PM1 nitrate to meteorological and chemical parameters and find that errors in both the predictions of relative humidity and free ammonia (FA ≡ NH3(g) + pNH4+ − 2 · pSO42-) are responsible for the poor agreement between modelled and measured values.
Language(s): English
Format: Digital (Free)Tags: Aerosols ; Atmosphere ; Meteorology ; Observations ; Weather forecasting ; Research ; Canada
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Latitudinal distributions of organic nitrogen and organic carbon in marine aerosols over the western North Pacific
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Miyazaki Y.; Kawamura K.; Jung J.; et al. - Copernicus GmbH, 2011Marine aerosol samples were collected over the western North Pacific along the latitudinal transect from 44° N to 10° N in late summer 2008 for measurements of organic nitrogen (ON) and organic carbon (OC) as well as isotopic ratios of total nitrogen (TN) and total carbon (TC). Increased concentrations of methanesulfonic acid (MSA) and diethylammonium (DEA+) at 40–44° N and subtropical regions (10–20° N) together with averaged satellite chlorophyll-a data and 5-day back trajectories suggest a significant influence of marine biological activities on aerosols in these regions. ON exhibited incre ...
[article]Latitudinal distributions of organic nitrogen and organic carbon in marine aerosols over the western North Pacific
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Available online: http://dx.doi.org/10.5194/acp-11-3037-2011
Y. Miyazaki ; K. Kawamura ; J. Jung ; H. Furutani ; M. Uematsu
in Atmospheric Chemistry and Physics (ACP) > Vol. 11. N° 7 [04/01/2011] . - p.3037-3049Marine aerosol samples were collected over the western North Pacific along the latitudinal transect from 44° N to 10° N in late summer 2008 for measurements of organic nitrogen (ON) and organic carbon (OC) as well as isotopic ratios of total nitrogen (TN) and total carbon (TC). Increased concentrations of methanesulfonic acid (MSA) and diethylammonium (DEA+) at 40–44° N and subtropical regions (10–20° N) together with averaged satellite chlorophyll-a data and 5-day back trajectories suggest a significant influence of marine biological activities on aerosols in these regions. ON exhibited increased concentrations up to 260 ngN m−3 in these marine biologically influenced aerosols. Water-insoluble organic nitrogen (WION) was found to be the most abundant nitrogen in the aerosols, accounting for 55 ± 16% of total aerosol nitrogen. In particular, the average WION/ON ratio was as high as 0.93 ± 0.07 at 40–44° N. These results suggest that marine biological sources significantly contributed to ON, a majority of which is composed of water-insoluble fractions in the study region. Analysis of the stable carbon isotopic ratios (δ13C) indicated that, on average, marine-derived carbon accounted for ~88 ± 12% of total carbon in the aerosols. In addition, the δ13C showed higher values (from −22 to −20‰) when ON/OC ratios increased from 0.15 to 0.35 in marine biologically influenced aerosols. These results clearly show that organic nitrogen is enriched in organic aerosols originated from an oceanic region with high biological productivity, indicating a preferential transfer of nitrogen-containing organic compounds from the sea surface to the marine atmosphere. Both WION concentrations and WION/water-insoluble organic carbon (WIOC) ratios tended to increase with increasing local wind speeds, indicating that sea-to-air emissions of ON via sea spray contribute significantly to the marine organic aerosols over the study region.
Language(s): English
Format: Digital (Free)Tags: Aerosols ; Nitrogen ; Ocean-atmosphere interaction ; Observations ; Pacific Ocean ; Region V - South-West Pacific
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Atmospheric degradation of 3-methylfuran: kinetic and products study
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Tapia A.; Villanueva F.; Salgado M.S.; et al. - Copernicus GmbH, 2011A study of the kinetics and products obtained from the reactions of 3-methylfuran with the main atmospheric oxidants has been performed. The rate coefficients for the gas-phase reaction of 3-methylfuran with OH and NO3 radicals have been determined at room temperature and atmospheric pressure (air and N2 as bath gases), using a relative method with different experimental techniques. The rate coefficients obtained for these reactions were (in units cm3 molecule−1 s−1) kOH = (1.13 ± 0.22) × 10−10 and kNO3 = (1.26 ± 0.18) × 10−11. Products from the reaction of 3-methylfuran with OH, NO3 and Cl at ...
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Saharan and Asian dust: similarities and differences determined by CALIPSO, AERONET, and a coupled climate-aerosol microphysical model
This study compares the properties of atmospheric dust from the Saharan deserts and the Asian deserts using data from CALIPSO and AERONET during 2006 and 2007 along with simulations using a coupled climate-microphysical sectional model. Saharan deserts are largely south of 30° N, while Asian ones are primarily north of 30° N, hence they experience different meteorological regimes. Saharan dust lifting occurs all year long, primarily due to subtropical weather systems. However, Asian dust is lifted mostly in spring when mid-latitude frontal systems lead to high winds. Rainfall is more abundant ...
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Analysis on the impact of aerosol optical depth on surface solar radiation in the Shanghai megacity, China
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Xu J.; Li C.; Shi H.; et al. - Copernicus GmbH, 2011This study investigated the decadal variation of the direct surface solar radiation (DiSR) and the diffuse surface solar radiation (DfSR) during 1961–2008 in the Shanghai megacity as well as their relationships to Aerosol Optical Depth (AOD) under clear-sky conditions. Three successive periods with unique features of long term variation of DiSR were identified for both clear-sky and all-sky conditions: a "dimming" period from the late 1960s to the mid 1980s, a "stabilization"/"slight brightening" period from the mid 1980s to the mid 1990s, and a "renewed dimming" period thereafter. During the ...
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Impact of model grid spacing on regional- and urban- scale air quality predictions of organic aerosol
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Stroud C.A.; Makar P.A.; Moran M.D.; et al. - Copernicus GmbH, 2011Regional-scale chemical transport model predictions of urban organic aerosol to date tend to be biased low relative to observations, a limitation with important implications for applying such models to human exposure health studies. We used a nested version of Environment Canada's AURAMS model (42- to- 15- to- 2.5-km nested grid spacing) to predict organic aerosol concentrations for a temporal and spatial domain corresponding to the Border Air Quality and Meteorology Study (BAQS-Met), an air-quality field study that took place in the southern Great Lakes region in the summer of 2007. The use o ...
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New particle formation events in semi-clean South African savannah
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 7. Vakkari V.; Laakso H.; Kulmala M.; et al. - Copernicus GmbH, 2011This study is based on 18 months (20 July 2006–5 February 2008) of continuous measurements of aerosol particle size distributions, air ion size distributions, trace gas concentrations and basic meteorology in a semi-clean savannah environment in Republic of South Africa. New particle formation and growth was observed on 69% of the days and bursts of non-growing ions/sub-10 nm particles on additional 14% of the days. This new particle formation frequency is the highest reported from boundary layer so far. Also the new particle formation and growth rates were among the highest reported in the li ...
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Gases com efeito de estufa, redução das emissões
Esporo, N° 151. CTA, 2011De acordo com um estudo realizado, seria possível diminuir o total das emissões relacionadas com o gado, em cerca de 12%, mediante simples melhoramentos na produção.
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Greenhouse gases, curbing emissions
Spore: the magazine for agricultural and rural development in ACP countries, N° 151. CTA, 2011Some 12% of total livestock-related emissions could be cut with simple improvements in production, says a study.
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Gaz à effet de serre, résorber les émissions
Spore: le magazine du développement agricole et rural des pays ACP, N°151. CTA, 2011D’après une étude, quelque 12 % des émissions totales imputables au bétail pourraient être supprimés grâce à de simples améliorations de la production, incluant l’adoption de pâtures plus nutritives et l’ajout de faibles quantités de résidus de récoltes ou de céréales.
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The 2009–2010 Arctic polar stratospheric cloud season: a CALIPSO perspective
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 5. Pitts M.C.; Poole L.R.; Dörnbrack A.; et al. - Copernicus GmbH, 2011Spaceborne lidar measurements from CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) are used to provide a vortex-wide perspective of the 2009–2010 Arctic PSC (polar stratospheric cloud) season to complement more focused measurements from the European Union RECONCILE (reconciliation of essential process parameters for an enhanced predictability of Arctic stratospheric ozone loss and its climate interactions) field campaign. The 2009–2010 Arctic winter was unusually cold at stratospheric levels from mid-December 2009 until the end of January 2010, and was one of only ...
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Insights into the secondary fraction of the organic aerosol in a Mediterranean urban area: Marseille
Atmospheric Chemistry and Physics (ACP), Vol. 11. N° 5. El Haddad I.; Marchand N.; Temime-Roussel B.; et al. - Copernicus GmbH, 2011A comprehensive aerosol characterization was conducted at Marseille during summer, including organic (OC) and elemental carbon (EC), major ionic species, radiocarbon (14C), water-soluble OC and HULIS (HUmic LIke Substances), elemental composition and primary and secondary organic markers. This paper is the second paper of a two-part series that uses this dataset to investigate the sources of Organic Aerosol (OA). While the first paper investigates the primary sources (El Haddad et al., 2010), this second paper focuses on the secondary fraction of the organic aerosol.
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