Michael Cusack

Variability of Particle Number, Black Carbon, and PM10, PM2.5, and PM1 Levels and Speciation: Influence of Road Traffic Emissions on Urban Air Quality

Measurements of particle number concentration (N), black carbon (BC), and PM 10 , PM 2.5 , and PM 1 levels and speciation were carried out at an urban background monitoring site in Barcelona. Daily variability of all aerosol monitoring parameters was highly influenced by road traffic emissions and meteorology. The levels of N, BC, PM X , CO, NO, and NO 2 increased during traffic rush hours, reflecting exhaust, and non-exhaust traffic emissions and then decreased by the effect of breezes and the reduction of traffic intensity. PM 2.5–10 levels did not decrease during the day as a result of dust resuspension by traffic and wind. N showed a second peak, registered in the afternoon and parallel to O 3 levels and solar radiation intensity, that may be attributed to photochemical nucleation of precursor gases. An increasing trend was observed for PM 1 levels from 1999 to 2006, related to the increase in the traffic flow and the diesel fleet in Barcelona. PM composition was highly influenced by road traffic emissions, with exhaust emissions being an important source of PM 1 and dust resuspension processes of PM 2.5–10 , respectively.

Intense winter atmospheric pollution episodes affecting the Western Mediterranean

The geographic location of the Western Mediterranean Basin and its peculiar topography, the climatic conditions and the intense anthropogenic and natural emissions of atmospheric pollutants are key factors necessary to interpret the atmospheric aerosol phenomenology over this area. During the cold season it is common to have severe atmospheric particulate matter (PM) pollution episodes (of an anthropogenic origin) affecting this region, not only in the urban and industrial areas but also in the regional and rural sites. During these episodes, the midday hourly PM(1) levels at regional background sites are in many cases higher than those at urban areas. Around 10% of the days under winter anticyclonic conditions registered similar PM(1) levels at the regional background than at the urban area and, sporadically the daily PM(1) levels at the regional background sites may exceed those at urban sites. Furthermore, the very high hourly PM(1) levels measured at regional background sites during these episodes are not regularly attained in the closest urban areas, which leads to the hypothesis that an important formation of secondary aerosols occurs during the transport of the polluted air masses towards the elevated rural sites. The interpretation of the variability of PM levels and composition (2002-2008) at one urban site (Barcelona) and at one regional background site (Montseny) allows us to illustrate the phenomenology of these scenarios, to quantify the mean annual contributions to the PM levels and to identify their main tracers. Ammonium nitrate appears to be the most abundant compound during these scenarios, although organic species and trace metals also increase markedly. Owing to the intensity, composition and recurrence of these atmospheric pollution episodes, important health, climatic and ecological implications may be derived.

Neural network model for the prediction of PM10 daily concentrations in two sites in the Western Mediterranean

An artificial neural network (ANN) was developed and tested to forecast PM10 daily concentration in two contrasted environments in NE Spain, a regional background site (Montseny), and an urban background site (Barcelona-CSIC), which was highly influenced by vehicular emissions. In order to predict 24-h average PM10 concentrations, the artificial neural network previously developed by Caselli et al. (2009) was improved by using hourly PM concentrations and deterministic factors such as a Saharan dust alert. In particular, the model input data for prediction were the hourly PM10 concentrations 1-day in advance, local meteorological data and information about air masses origin. The forecasted performance indexes for both sites were calculated and they showed better results for the regional background site in Montseny (R(2)=0.86, SI=0.75) than for urban site in Barcelona (R(2)=0.73, SI=0.58), influenced by local and sometimes unexpected sources. Moreover, a sensitivity analysis conducted to understand the importance of the different variables included among the input data, showed that local meteorology and air masses origin are key factors in the model forecasts. This result explains the reason for the improvement of ANNs forecasting performance at the Montseny site with respect to the Barcelona site. Moreover, the artificial neural network developed in this work could prove useful to predict PM10 concentrations, especially, at regional background sites such as those on the Mediterranean Basin which are primarily affected by long-range transports. Hence, the artificial neural network presented here could be a powerful tool for obtaining real time information on air quality status and could aid stakeholders in their development of cost-effective control strategies.

Urban NH3 levels and sources in six major Spanish cities.

A detailed spatial and temporal assessment of urban NH3 levels and potential emission sources was made with passive samplers in six major Spanish cities (Barcelona, Madrid, A Coruña, Huelva, Santa Cruz de Tenerife and Valencia). Measurements were conducted during two different periods (winter-autumn and spring-summer) in each city. Barcelona showed the clearest spatial pattern, with the highest concentrations in the old city centre, an area characterised by a high population density and a dense urban architecture. The variability in NH3 concentrations did not follow a common seasonal pattern across the different cities. The relationship of urban NH3 with SO2 and NOX allowed concluding on the causes responsible for the variations in NH3 levels between measurement periods observed in Barcelona, Huelva and Madrid. However, the factors governing the variations in A Coruña, Valencia and Santa Cruz de Tenerife are still not fully understood. This study identified a broad variability in NH3 concentrations at the city-scale, and it confirms that NH3 sources in Spanish urban environments are vehicular traffic, biological sources (e.g. garbage containers), wastewater treatment plants, solid waste treatment plants and industry. The importance of NH3 monitoring in urban environments relies on its role as a precursor of secondary inorganic species and therefore PMX. Further research should be addressed in order to establish criteria to develop and implement mitigation strategies for cities, and to include urban NH3 sources in the emission inventories.

Detailed comparison of OC/EC aerosol at an urban and a rural Czech background site during summer and winter

Winter and summer measurements of organic carbon and elemental carbon (OC and EC) in PM2.5 were performed in parallel at two sites, the rural background station Košetice and the Prague-Suchdol urban background site, with a 2-h time resolution using semi-online field OC/EC analysers. Seasonal and site differences were found in the OC and EC contents of PM2.5. Overall, the highest concentrations of both OC and EC were during winter at the urban site. The average urban impact was 50% for OC and 70% for EC. The summer season gives similar concentrations of OC at both sites. However, higher concentrations of EC, caused by higher traffic, were found at the urban site with an average urban increase of 50%. Moreover, an analysis of four OC fractions depending on the volatility (OC1 - most volatile, OC4 - least volatile) and pyrolytic carbon (PC) is provided. A similar level of each OC fraction at both sites was found in summer, except for higher OC1 at urban and higher PC at the rural site. In winter, the differences between the urban and rural sites were dominated by a large increase of the OC1 fraction in comparison with the rural site. A diurnal pattern of concentration and share of OC1 and PC suggests a prevailing influence of local sources on their concentrations at the urban site in winter. The OC3 and OC4 diurnal cycles suggest their more regional or long range transport origin in both seasons. The prevalent influence of OC1 at any urban site has not been previously reported. The minimisation of semi-volatile carbon losses during semi-continuous sampling and analysis, in comparison with off-line sampling methods, is a probable reason for the observed differences.

Variability of sub-micrometer particle number size distributions and concentrations in the Western Mediterranean regional background

ABSTRACT This study focuses on the daily and seasonal variability of particle number size distributions and concentrations, performed at the Montseny (MSY) regional background station in the western Mediterranean from October 2010 to June 2011. Particle number concentrations at MSY were shown to be within range of various other sites across Europe reported in literature, but the seasonality of the particle number size distributions revealed significant differences. The Aitken mode is the dominant particle mode at MSY, with arithmetic mean concentrations of 1698 cm3, followed by the accumulation mode (877 cm−3) and the nucleation mode (246 cm−3). Concentrations showed a strong seasonal variability with large increases in particle number concentrations observed from the colder to warmer months. The modality of median size distributions was typically bimodal, except under polluted conditions when the size distribution was unimodal. During the colder months, the daily variation of particle number size distributions are strongly influenced by a diurnal breeze system, whereby the Aitken and accumulation modes vary similarly to PM1 and BC mass concentrations, with nocturnal minima and sharp day-time increases owing to the development of a diurnal mountain breeze. Under clean air conditions, high levels of nucleation and lower Aitken mode concentrations were measured, highlighting the importance of new particle formation as a source of particles in the absence of a significant condensation sink. During the warmer months, nucleation mode concentrations were observed to be relatively elevated both under polluted and clean conditions due to increased photochemical reactions, with enhanced subsequent growth owing to elevated concentrations of condensable organic vapours produced from biogenic volatile organic compounds, indicating that nucleation at MSY does not exclusively occur under clean air conditions. Finally, mixing of air masses between polluted and non-polluted boundary layer air, and brief changes in the air mass being sampled gave rise to unusual particle number size distributions, with specific cases of such behaviour discussed at length.

Mechanisms of Climate Variability, Air Quality and Impacts of Atmospheric Constituents in the Mediterranean Region

This chapter describes the physicochemical mechanisms that formulate the air quality over the Mediterranean region and the resulted impacts on the regional climate. At first, a detailed description of the teleconnections and regional flow patterns that dominate in the region is provided. The dominant flow patterns during the different seasons of the year determine the transport paths of air pollutants and aerosols towards and across the study area. The analysis on the characteristics of the air pollution transport is separated for the different parts of the Mediterranean region (eastern, western and entire), since the sources of pollutants that reach at different points in the region vary, while specific pollutant transport paths may influence the wider Mediterranean area. Similarities and differences in patterns are discussed. The air quality over the region, as recorded from black/organic carbon, ozone, aerosol observations, is extensively discussed, along with seasonal variabilities and annual trends. There is particular discussion on the suspension of naturally-produced aerosols and especially desert dust particles in the region and their spatial influence on the aerosol levels. At the last part of the chapter, the major impacts of the transport and transformation processes (natural and anthropogenic pollutants) on the regional climate are discussed. The impacts of aerosols are distinguished in direct (the impacts on radiation budget), health (the amounts of inhaled particles and impacts on health) and indirect effects (impacts on clouds and precipitation), are discussed on qualitative and quantitative way.

Accumulation of Carbonates Contributes to Coastal Vegetated Ecosystems Keeping Pace With Sea Level Rise in an Arid Region (Arabian Peninsula)

This research was supported by a project funded by Saudi Aramco and baseline funding from King Abdullah University of Science and Technology (KAUST). O. S. was supported by an ARC DECRA (DE170101524). Funding was provided to PM by the Generalitat de Catalunya (grant 2014 SGR‐1356) and an Australian Research Council LIEF Project (LE170100219). AAO was supported by a PhD scholarship from Obra Social “LaCaixa”. This work is contributing to the ICTA ‘Unit of Excellence’ (MinECo, MDM2015‐0552). We thank A. Qasem and P. Priahartato, Saudi Aramco, for support and advice on sampling design; R. Lindo, R. Magalles, P. Bacquiran, S. Ibrahim, and M. Lopez, at the Marine Studies section of the Center for Environment and Water of King Fahd University of Petroleum and Minerals; and Z. Batang and staff from the Coastal and Marine Resources core lab at KAUST for help with sampling. We thank I. Schulz, N. Geraldi, K. Rowe, S. Roth, M. Ennasri, D. Prabowo, and I. Mendia for help with laboratory analyses. We wish to thank the two anonymous reviewers, as well as Editor in chief M. Goni, for their precious comments/suggestions for the improvement of the manuscript. The data sets, including 14C and 210Pb data, CaCO3 concentration values, porosities, and CaCO3 depth profiles for all cores, are available in the open repository Pangaea (Saderne et al., 2018; https://doi.pangaea.de/10.1594/PANGAEA.887043).

Single Usage of a Kitchen Degreaser Can Alter Indoor Aerosol Composition for Days

To the best of our knowledge, this study represents the first observation of multiday persistence of an indoor aerosol transformation linked to a kitchen degreaser containing monoethanol amine (MEA). MEA remaining on the cleaned surfaces and on a wiping paper towel in a trash can was able to transform ammonium sulfate and ammonium nitrate into (MEA)2SO4 and (MEA)NO3. This influence persisted for at least 60 h despite a high average ventilation rate. The influence was observed using both offline (filters, impactors, and ion chromatography analysis) and online (compact time-of-flight aerosol mass spectrometer) techniques. Substitution of ammonia in ammonium salts was observed not only in aerosol but also in particles deposited on a filter before the release of MEA. The similar influence of other amines is expected based on literature data. This influence represents a new pathway for MEA exposure of people in an indoor environment. The stabilizing effect on indoor nitrate also causes higher indoor exposure to fine nitrates.