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The effect of nanogel colloidal and dissolved organic matter The aerosol generated from seawater proxies enriched with marine exudate presented organic volume fractions on the order of 8–37%, as derived by applying a simple mixing rule. The hygroscopic growth and cloud condensation nuclei (CCN) activity of the marine organics-enriched particles where 9–17% and 5–24% lower, respectively, than those of the aerosol produced from artificial seawater devoid of exudate. Experiments in a companion paper indicated that the cloud nuclei formation could be enhanced in diatom bloom areas because of the increase in the primary particle production induced by marine organics. The experiments in the present study, however, indicate that the impacts of such an enhancement would be counteracted by the reduction in the CCN activity of the primary particles enriched in marine organics. The extent of the effect of the biogenic matter on the particle behaviour was dependent on the seawater organic concentration and type of algal exudate. Aerosol produced from seawater proxies containing diatomaceous exudate presented higher hydrophobicity and lower CCN activity than those enriched with nanoplankton exudate. The organic fraction of the particles was found to correlate with the seawater organic concentration, without observing saturation of the particle organic mass fraction even for unrealistically high organic matter concentration in seawater. These findings are indicative that discrepancies on the composition of the primary aerosol between different studies could partly be explained by the difference in the nature and concentration of the organic matter in the source seawater employed. Consistently across the experiments, theoretical analysis based on the Köhler model predicted a reduction in the primary marine aerosol CCN activity upon the incorporation of marine organics into the particle composition. This effect is consequence of the replacement of small inorganic sea salt molecules by large molar mass organic molecules, together with a moderate suppression of the surface tension at the point of activation of 5–0.5%, which leads to a dominance of the reduction in the dissolved solute in the Raoult term.

In April–July 2008, intensive measurements were made of atmospheric composition and chemistry in Sabah, Malaysia, as part of the "Oxidant and particle photochemical processes above a South-East Asian tropical rain forest" (OP3) project. Fluxes and concentrations of trace gases and particles were made from and above the rain forest canopy at the Bukit Atur Global Atmosphere Watch station and at the nearby Sabahmas oil palm plantation, using both ground-based and airborne measurements. Here, the measurement and modelling strategies used, the characteristics of the sites and an overview of data obtained are described. Composition measurements show that the rainforest site was not impacted by significant sources of anthropogenic pollution, and this is confirmed by satellite retrievals of NO2 and HCHO. The dominant modulators of atmospheric chemistry at the rain forest site were therefore emissions of BVOCs and soil emissions of reactive nitrogen oxides. At the observed BVOC:NOx volume mixing ratio (~104 pptv/pptv), current chemical models suggest that daytime maximum OH concentrations should be ca. 105 radicals cm−3, but observed OH concentrations were an order of magnitude greater than this. We confirm, therefore, previous measurements which suggest that an unexplained source of OH must exist above tropical forests and continue to interrogate the data to find explanations for this.

Measurements of aerosol properties were made in aged polluted and clean background air masses encountered at the North Norfolk (UK) coastline during the second field campaign of the Tropospheric ORganic CHemistry project (TORCH2) in May 2004. Hygroscopic growth factor (GF) measurements were performed at 90% relative humidity (RH) for D0=27?217 nm particles using a Hygroscopicity Tandem Differential Mobility Analyser (HTDMA), while the aerosol composition was simultaneously measured with an Aerodyne aerosol mass spectrometer (Q-AMS). During the clean background events the aerosol was characterised by little size dependence of properties with generally large GFs and inorganic sulphate being the dominant compound. In aged polluted air masses the particles were dominated by inorganic sulphate and nitrate at larger sizes, whereas organics were the largest fraction in smaller particles, thus explaining the trend of smaller GFs at smaller sizes. Organics do contribute to the hygroscopic growth, particularly at small sizes, but generally the dominant contribution to growth at 90% RH comes from inorganic salts. The ZSR mixing rule was used to predict GFs based on the chemical composition, theoretical GFs of pure inorganic salts and a "bulk" GF of ~1.20 for the organics. Good quantitative closure with HTDMA measurements as a function of both particle size and time was achieved in the absence of nitrate. However, GFs were clearly overpredicted at times when a significant fraction of nitrate was present. After careful considerations we attribute the overprediction to substantial evaporation losses of ammonium nitrate in the HTDMA instrument. If true, this implies that the ZSR predictions based on composition might be more representative of the actual "bulk" behaviour of undisturbed ambient particles than the HTDMA measurements. The simplified model approach using the ZSR rule and a constant organic growth factor made high size and time resolution possible, which has proven to be essential for a valid closure study. The ZSR mixing rule appears to be sufficiently accurate, as the GF predictions are more sensitive to the exact GFs of the inorganic compounds than to the growth factor of the moderately hygroscopic organics. Therefore a more detailed analysis and modelling of the organic fraction at the expense of time and size resolution is not worth the effort for an aged aerosol and discrepancies in either direction might even be cancelled out by averaging.

© 2019 Author(s). The Atmospheric Pollution and Human Health in a Chinese Megacity (APHH-Beijing) programme is an international collaborative project focusing on understanding the sources, processes and health effects of air pollution in the Beijing megacity. APHH-Beijing brings together leading China and UK research groups, state-of-the-art infrastructure and air quality models to work on four research themes: (1) sources and emissions of air pollutants; (2) atmospheric processes affecting urban air pollution; (3) air pollution exposure and health impacts; and (4) interventions and solutions. Themes 1 and 2 are closely integrated and support Theme 3, while Themes 1-3 provide scientific data for Theme 4 to develop cost-effective air pollution mitigation solutions. This paper provides an introduction to (i) the rationale of the APHH-Beijing programme and (ii) the measurement and modelling activities performed as part of it. In addition, this paper introduces the meteorology and air quality conditions during two joint intensive field campaigns-a core integration activity in APHH-Beijing. The coordinated campaigns provided observations of the atmospheric chemistry and physics at two sites: (i) the Institute of Atmospheric Physics in central Beijing and (ii) Pinggu in rural Beijing during 10 November-10 December 2016 (winter) and 21 May-22 June 2017 (summer). The campaigns were complemented by numerical modelling and automatic air quality and low-cost sensor observations in the Beijing megacity. In summary, the paper provides background information on the APHH-Beijing programme and sets the scene for more focused papers addressing specific aspects, processes and effects of air pollution in Beijing.

International audience; The North Atlantic Marine Boundary Layer Experiment (NAMBLEX), involving over 50 scientists from 12 institutions, took place at Mace Head, Ireland (53.32° N, 9.90° W), between 23 July and 4 September 2002. A wide range of state-of-the-art instrumentation enabled detailed measurements of the boundary layer structure and atmospheric composition in the gas and aerosol phase to be made, providing one of the most comprehensive in situ studies of the marine boundary layer to date. This overview paper describes the aims of the NAMBLEX project in the context of previous field campaigns in the Marine Boundary Layer (MBL), the overall layout of the site, a summary of the instrumentation deployed, the temporal coverage of the measurement data, and the numerical models used to interpret the field data. Measurements of some trace species were made for the first time during the campaign, which was characterised by predominantly clean air of marine origin, but more polluted air with higher levels of NOx originating from continental regions was also experienced. This paper provides a summary of the meteorological measurements and Planetary Boundary Layer (PBL) structure measurements, presents time series of some of the longer-lived trace species (O3, CO, H2, DMS, CH4, NMHC, NOx, NOy, PAN) and summarises measurements of other species that are described in more detail in other papers within this special issue, namely oxygenated VOCs, HCHO, peroxides, organo-halogenated species, a range of shorter lived halogen species (I2, OIO, IO, BrO), NO3 radicals, photolysis frequencies, the free radicals OH, HO2 and (HO2+? RO2), as well as a summary of the aerosol measurements. NAMBLEX was supported by measurements made in the vicinity of Mace Head using the NERC Dornier-228 aircraft. Using ECMWF wind-fields, calculations were made of the air-mass trajectories arriving at Mace Head during NAMBLEX, and were analysed together with both meteorological and trace-gas measurements. In this paper a chemical climatology for the duration of the campaign is presented to interpret the distribution of air-mass origins and emission sources, and to provide a convenient framework of air-mass classification that is used by other papers in this issue for the interpretation of observed variability in levels of trace gases and aerosols.

Several zero-dimensional box-models with different levels of chemical complexity, based on the Master Chemical Mechanism (MCM), have been used to study the chemistry of OH and HO2 in a coastal environment in the Northern Hemisphere. The models were constrained to and compared with measurements made during the NAMBLEX campaign ( Mace Head, Ireland) in summer 2002. The base models, which were constrained to measured CO, CH4 and NMHCs, were able to reproduce [ OH] within 25%, but overestimated [HO2] by about a factor of 2. Agreement was improved when the models were constrained to oxygenated compounds ( acetaldehyde, methanol and acetone), highlighting their importance for the radical budget. When the models were constrained to measured halogen monoxides (IO, BrO) and used a more detailed, measurements-based, treatment to describe the heterogeneous uptake, modelled [OH] increased by up to 15% and [HO2] decreased by up to 30%. The actual impact of halogen monoxides on the modelled concentrations of HOx was dependant on the uptake coefficients used for HOI, HOBr and HO2. Better agreement, within the combined uncertainties of the measurements and of the model, was achieved when using high uptake coefficients for HO2 and HOI (gamma(HO2)= 1, gamma(HOI)= 0(6). A rate of production and destruction analysis of the models allowed a detailed study of OH and HO2 chemistry under the conditions encountered during NAMBLEX, showing the importance of oxygenates and of XO ( where X=I, Br) as coreactants for OH and HO2 and of HOX photolysis as a source for OH. 029TS Times Cited:16 Cited References Count:55