Source apportionment of particulate matter (PM2.5) in an urban area using dispersion,receptor and inverse modelling

Air pollution emission inventories are the basis for air quality assessment and management strategies. The quality of the inventories is of great importance since these data are essential for air pollution impact assessments using dispersion models. In this study, the quality of the emission inventory for fine particulates (PM_2.5) is assessed: first, using the calculated source contributions from a receptor model; second, using source apportionment from a dispersion model; and third, by applying a simple inverse modelling technique which utilises multiple linear regression of the dispersion model source contributions together with the observed PM_2.5 concentrations. For the receptor modelling the chemical composition of PM_2.5 filter samples from a measurement campaign performed between January 2004 and April 2005 are analysed. Positive matrix factorisation is applied as the receptor model to detect and quantify the various source contributions. For the same observational period and site, dispersion model calculations using the Air Quality Management system, AirQUIS, are performed. The results identify significant differences between the dispersion and receptor model source apportionment, particularly for wood burning and traffic induced suspension. For wood burning the receptor model calculations are lower, by a factor of 0.54, but for the traffic induced suspension they are higher, by a factor of 7.1. Inverse modelling, based on regression of the dispersion model source contributions and the PM_2.5 concentrations, indicates similar discrepancies in the emissions inventory. In order to assess if the differences found at the one site are generally applicable throughout Oslo, the individual source category emissions are rescaled according to the receptor modelling results. These adjusted PM_2.5 concentrations are compared with measurements at four independent stations to evaluate the updated inventory. Statistical analysis shows improvement in the estimated concentrations for PM_2.5 at all sites. Similarly, inverse modelling is applied at these independent sites and this confirms the validity of the receptor model results.     

Urban aerosol evolution and particle formation during wintertime temperature inversions

Aerosol temporal and spatial distributions during wintertime temperature inversions in Gothenburg, Sweden, have been characterized by ground-based and airborne particle measurements combined with lidar measurements. Ground inversions frequently developed during evenings and nights with stable cold conditions, and the low wintertime insolation often resulted in near neutral boundary layer conditions during day-time. Under these conditions ground level aerosol concentrations peaked during morning rush hours and often remained relatively high throughout the day due to inefficient ventilation. The particle number concentrations decreased slowly with increasing altitude within the boundary layer, and measurements slightly above the boundary layer suggested limited entrainment of polluted air into the free troposphere. High concentrations of ultrafine particles were observed throughout the boundary layer up to altitudes of 1100 m, which suggested that nucleation took place within the residual layer during the night and early morning. Recently formed particles were also observed around midday when the layer near ground was ventilated by mixing into the boundary layer, which indicated that ultrafine particles were either transported down from the residual layer to ground level or formed when the polluted surface layer mixed with the cleaner air above.     

Modeling of temporal variations of vertical concentration profile of 7Be in the atmosphere

Study of the vertical concentration profile and of the deposition of cosmogenic radionuclides provides information on the vertical transport in the stratosphere and troposphere and the processes of scavenging of aerosol particles by precipitation. Information on the distribution of atmospheric aerosols is important for the understanding of the physical processes relating to the studies in weather climate, air pollution, and aerosol physics. In this work the one-dimensional steady-state model of vertical concentration profile was established and the values of turbulent diffusion coefficient and scavenging coefficient determined by model using experimental data of the ⁷Be monthly average atmospheric activity concentrations and monthly deposition fluxes in Bratislava are presented. The temporal variations of the vertical distribution profiles of ⁷Be for each month are also calculated.     

Effects of a herbicide-insecticide mixture in freshwater microcosms: risk assessment and ecological effect chain

Effects of chronic application of a mixture of the herbicide atrazine and the insecticide lindane were studied in indoor freshwater plankton-dominated microcosms. The macroinvertebrate community was seriously affected at all but the lowest treatment levels, the zooplankton community at the three highest treatment levels, with crustaceans, caddisflies and dipterans being the most sensitive groups. Increased abundance of the phytoplankton taxa Cyclotella sp. was found at the highest treatment level. Threshold levels for lindane, both at population and community level, corresponded well with those reported in the literature. Atrazine produced fewer effects than expected, probably due to decreased grazer stress on the algae as a result of the lindane application. The safety factors set by the Uniform Principles for individual compounds were also found to ensure protection against chronic exposure to a mixture of a herbicide and insecticide at community level, though not always at the population level.     

Characterizing pesticide sorption and degradation in microscale biopurification systems using column displacement experiments

Biopurification systems treating pesticide contaminated water are very efficient, however they operate as a black box. Processes inside the system are not yet characterized. To optimize the performance, knowledge of degradation and retention processes needs to be generated. Therefore, displacement experiments were carried out for four pesticides (isoproturon, bentazone, metalaxyl, linuron) in columns containing different organic mixtures. Bromide, isoproturon and bentazone breakthrough curves (BTCs) were well described using the convection-dispersion equation (CDE) and a first-order degradation kinetic approach. Metalaxyl and linuron BTCs were well described using the CDE model expanded with Monod-type kinetics. Freundlich sorption, first-order degradation and Monod kinetics coefficients were fitted to the BTCs. Fitted values of the distribution coefficient K_f,column were much lower than those determined from batch experiments. Based on mobility, pesticides were ranked as: bentazone > metalaxyl - isoproturon > linuron. Based on degradability, pesticides were ranked as: linuron > metalaxyl - isoproturon > bentazone.     

How to assess exposure of aquatic organisms to manufactured nanoparticles?

Ecological risk of chemicals is measured by the quotient of predicted no-effect concentrations and predicted exposure concentrations, which are hard to assess for manufactured nanomaterials (NMs). This paper proposes modifications to currently used models, in order to make them suitable for estimating exposure concentrations of NMs in the aquatic environment. We have evaluated the adequacy of the current guidance documents for use with NMs and conclude that nano-specific fate processes, such as sedimentation and dissolution need to be incorporated. We have reviewed the literature on sedimentation and dissolution of NMs in environmentally relevant systems. We deduce that the overall kinetics of water-sediment transport of NMs should be close to first order. The lack of data on dissolution of NMs under environmentally realistic conditions calls for a pragmatic decision on which rates to be used in modeling. We find that first order removal kinetics for dissolution seems adequate. Based on limited data from literature, probable removal rates range from 0 to 10(-4)s(-1) for sedimentation, and from 0 to 10(-5)s(-1) for dissolution. Further experimental data at environmentally relevant conditions for sedimentation and dissolution of NMs is needed.     

Tipping Toward Sustainability: Emerging Pathways of Transformation

This article explores the links between agency, institutions, and innovation in navigating shifts and large-scale transformations toward global sustainability. Our central question is whether social and technical innovations can reverse the trends that are challenging critical thresholds and creating tipping points in the earth system, and if not, what conditions are necessary to escape the current lock-in. Large-scale transformations in information technology, nano- and biotechnology, and new energy systems have the potential to significantly improve our lives; but if, in framing them, our globalized society fails to consider the capacity of the biosphere, there is a risk that unsustainable development pathways may be reinforced. Current institutional arrangements, including the lack of incentives for the private sector to innovate for sustainability, and the lags inherent in the path dependent nature of innovation, contribute to lock-in, as does our incapacity to easily grasp the interactions implicit in complex problems, referred to here as the ingenuity gap. Nonetheless, promising social and technical innovations with potential to change unsustainable trajectories need to be nurtured and connected to broad institutional resources and responses. In parallel, institutional entrepreneurs can work to reduce the resilience of dominant institutional systems and position viable shadow alternatives and niche regimes.     

Study of soil-plant transfer of 226Ra under greenhouse conditions

A soil-plant transfer study was performed using soil from a former uranium ore processing factory in South Bohemia. We present the results from greenhouse experiments which include estimates of the time required for phytoremediation. The accumulation of ²²⁶Ra by different plant species from a mixture of garden soil and contaminated substrate was extremely variable, ranging from 0.03 to 2.20 Bq ²²⁶Ra/g DW. We found differences in accumulation of ²²⁶Ra between plants from the same genus and between cultivars of the same plant species. The results of ²²⁶Ra accumulation showed a linear relation between concentration of ²²⁶Ra in plants and concentration of ²²⁶Ra in soil mixtures. On the basis of these results we estimated the time required for phytoremediation, but this appears to be too long for practical purposes.     

Chemical contamination and the ecological quality of surface water

In the assessment of the quality of surface waters, the typical procedure is that the concentration of contaminants in the surface water is monitored and subsequently compared with their respective Maximum Permissible Concentrations (MPCs). If the MPCs are not exceeded the water quality is considered to be safe. But can we be certain that this is true?We compared MPCs to observed and calculated effects of measured contaminants in Dutch surface waters and showed that effects of mixtures can cause a daphnid population to go extinct within 30 h of exposure even when MPCs are not exceeded. We conclude that there are shortcomings underlying the concepts of the MPCs. And that the MPCs aim to protect 95% of all species is not met.     

A novel approach for characterization of polycyclic aromatic hydrocarbon (PAH) pollution patterns in sediments from Guanabara Bay, Rio de Janeiro, Brazil

A novel multivariate method based on principal component analysis of pre-processed sections of chromatograms is used to characterize the complex PAH pollution patterns in sediments from Guanabara Bay, Brazil. Five distinct sources of 3- to 6-ring PAHs could be revealed. The harbour is the most contaminated site in the bay, its plume stretches in a South West to North East direction and the chemical profile indicates mainly pyrogenic sources mixed with a fraction of high-molecular-weight petrogenic PAHs. Rio São João de Meriti is the second largest source of PAHs, and introduces mainly a fraction of low-molecular-weight petrogenic PAHs from the western region of Rio de Janeiro. The sites close to the ruptured pipeline at the Duque de Caxias Refinery show a distinctive pollution pattern indicating a heavy petroleum fraction. The method also led to the identification of new potential indicator ratios also involving coeluting peaks (e.g., triphenylene and chrysene).