Student Debt and Geographic Disadvantage: Disparities by Rural, Suburban, and Urban Background*

Abstract. Carbon-containing particles have deleterious effects on both Earth's climate and human health. In Europe, the main sources of light-absorbing carbon (LAC) emissions are the transport (67%) and residential (25%) sectors. Information on the spatiotemporal variability of LAC particles in urban areas is relevant for air quality management and to better diagnose the population exposure to these particles. This study reports on results of an intensive field campaign conducted at four sites (two kerbside stations, one urban background site and a rural station) in Stockholm, Sweden, during the spring 2006. Light-absorbing carbon mass (MLAC) concentrations were measured with custom-built Particle Soot Absorption Photometers (PSAP). The spatiotemporal variability of MLAC concentrations was explored by examining correlation coefficients (R), coefficients of divergence (COD), and diurnal patterns at all sites. Simultaneous measurements of NOx, PM10, PM2.5, and meteorological variables were also carried out at the same locations to help characterize the LAC emission sources. Hourly mean (± standard deviation) MLAC concentrations ranged from 0.36±0.50 at the rural site to 5.39±3.60 μg m−3 at the street canyon site. Concentrations of LAC between urban sites were poorly correlated even for daily averages (R<0.70), combined with highly heterogeneously distributed concentrations (COD>0.30) even at spatial scales of few kilometers. This high variability is connected to the distribution of emission sources and processes contributing to the LAC fraction at these sites. At urban sites, MLAC tracked NOx levels and traffic density well and mean MLAC/PM2.5 ratios were larger (26–38%) than at the background sites (4–10%). The results suggest that vehicle exhaust emissions are the main responsible for the high MLAC concentrations found at the urban locations whereas long-range transport (LRT) episodes of combustion-derived particles can generate a strong increase of levels at background sites. To decrease pollution levels at kerbside and urban background locations in Stockholm, we recommend abatement strategies that target reductions of vehicle exhaust emissions, which are the main contributors to MLAC and NOx concentrations.

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Development of the city-scale chemistry transport model CityChem-EPISODE and its application to the city of Hamburg

10.5194/gmd-2018-8 ◽

2018 ◽

Cited By ~ 2

Author(s):

Matthias Karl

Keyword(s):

Air Quality ◽

Urban Area ◽

Transport Model ◽

Dispersion Model ◽

Temporal Correlation ◽

Urban Atmosphere ◽

Aerosol Formation ◽

Urban Background ◽

New Model ◽

The City

Abstract. This paper describes the City-scale Chemistry (CityChem) extension of the urban dispersion model EPISODE with the aim to enable chemistry/transport simulations of multiple reactive pollutants on urban scales. The new model is called CityChem-EPISODE. The primary focus is on the simulation of urban ozone concentrations. Ozone is produced in photochemical reaction cycles involving nitrogen oxides (NOx) and volatile organic compounds (VOC) emitted by various anthropogenic activities in the urban area. The performance of the new model was evaluated with a series of synthetic tests and with a first application to the air quality situation in the city of Hamburg, Germany. The model performs fairly well for ozone in terms of temporal correlation and bias at the air quality monitoring stations in Hamburg. In summer afternoons, when photochemical activity is highest, modelled median ozone at an inner-city urban background station was about 30 % lower than the observed median ozone. Inaccuracy of the computed photolysis frequency of nitrogen dioxide (NO2) is the most probable explanation for this. CityChem-EPISODE reproduces the spatial variation of annual mean NO2 concentrations between urban background, traffic and industrial stations. However, the temporal correlation between modelled and observed hourly NO2 concentrations is weak for some of the stations. For daily mean PM10, the performance of CityChem-EPISODE is moderate due to low temporal correlation. The low correlation is linked to uncertainties in the seasonal cycle of the anthropogenic particulate matter (PM) emissions within the urban area. Missing emissions from domestic heating might be an explanation for the too low modelled PM10 in winter months. Four areas of need for improvement have been identified: (1) dry and wet deposition fluxes; (2) treatment of photochemistry in the urban atmosphere; (3) formation of secondary inorganic aerosol (SIA); and (4) formation of biogenic and anthropogenic secondary organic aerosol (SOA). The inclusion of secondary aerosol formation will allow for a better sectorial attribution of observed PM levels. Envisaged applications of the CityChem-EPISODE model are urban air quality studies, environmental impact assessment, sensitivity analysis of sector-specific emission and the assessment of local and regional emission abatement policy options.

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