Limestone surfaces in built-up environment as indicators of atmospheric pollution

The concentration of sulphate on limestone surfaces of the external walls of churches in Malta is shown to be related to their position and distance from a power station, the main local point source of sulphur dioxide pollution. Limestone powder collected from these surfaces was examined for the presence of particles which, under low-power optical microscopy, appear as shiny black amorphous bodies which were interpreted as soot particles; the abundance of these bodies was expressed as a black particle count (BPC). The degree of sulphation and BPC were shown to be correlated with each other and both appeared to be strongly dependent on the prevailing wind. The BPC contour map indicated an important contribution to the parameter from vehicular traffic. It is suggested that the degree of sulphation and BPC of limestone surfaces from the built environment should function as environmental indicators of the relative air quality with respect to SO₂ and soot pollution. This data is possibly more accurately representative of the relative long-term air-quality status of different areas of habitation than that deduced from single or episodic measurements of atmospheric pollutant levels.     

Metallsorption an Illit und Metallfreisetzung unter Einwirken der Aminosäuren Glycin und Histidin

The heavy metal ions Zn(II), Pb(II), Cr(III) and Hg(II) were examined in regard of their adsorption behaviour towards Kaolin W from Lohrheim (51% illite, 31% kaolinite and 18% quarz). By means of the Langmuir and Freundlich models the determined adsorption isothermes could be linearized. The ability of glycine and histidine solutions to release heavy metal ions, pre-adsorbed on Kaolin W (36,1–2300 mg kg^?1 Zn, Pb, Cr and Hg), was specified. It was found a low influence of glycine, but an evident influence of histidine to the metal release, expecially of Pb and Cr, depending on the metalcoating, metal-amino acid-ratio, experimental pH and testing period. The highest remobilisation fraction, up to 98%, could be found in the case of Zn. This elucidates an enhancement of the zinc release compared with the blank solution, without containing amino acids, to a factor of maximal 9,3. As far as Pb and Cr were concerned the histidine extraction exeeded the remobilisation in the blank solution by a maximum of 50,8 or 40. As Hg develops strong covalent bondings to illite by OH-bridges, the release of Hg was not affected by the amino acids.     

Gas-phase organics in environmental tobacco smoke: 2. Exposure-relevant emission factors and indirect exposures from habitual smoking

Sorption of emitted gas-phase organic compounds onto material surfaces affects environmental tobacco smoke (ETS) composition and exposures indoors. We have introduced a new metric, the exposure relevant emission factor (EREF) that accounts for sorptive uptake and reemission to give the mass of individual ETS constituents available for exposure over a day in which smoking occurs. This paper describes month-long experiments to investigate sorption effects on EREFs and potential ETS exposures under habitual smoking conditions. Cigarettes were smoked in a 50-m³ furnished room over a 3-h period 6–7 days per week, with continuous ventilation at 0.3, 0.6, or 2.1 h⁻¹. Organic gas concentrations were measured every few days over 4-h “smoking”, 10-h “post-smoking” and 10-h “background” periods. Concentration patterns of volatile ETS components including 1,3-butadiene, benzene and acrolein were similar to those calculated for a theoretical non-sorbing tracer, indicating limited sorption. Concentrations of ETS tracers, e.g. 3-ethenylpyridine (3-EP) and nicotine, and lower volatility toxic air contaminants including phenol, cresols, and naphthalene increased as experiments progressed, indicating mass accumulation on surfaces and higher desorption rates. Daily patterns stabilized after week 2, yielding a steady daily cycle of ETS concentrations associated with habitual smoking. EREFs for sorbing compounds were higher under steady cycle versus single-day smoking conditions by 50% for 3-EP, and by 2–3 times for nicotine, phenol, cresols, naphthalene, and methylnaphthalenes. Our results provide relevant information about potential indirect exposures from residual ETS (non-smoker enters room shortly after smoker finishes) and from reemission, and their importance relative to direct exposures (non-smoker present during smoking). Under the conditions examined, indirect exposures accounted for a larger fraction of total potential exposures for sorbing versus non-sorbing compounds, and at lower versus higher ventilation rates. Increasing ventilation can reduce indirect exposures to very low levels for non-sorbing ETS components, but indirect routes accounted for 50% of potential nicotine exposures during non-smoking periods at all ventilation rates.     

Water quality associated public health risk in Bo, Sierra Leone

Human health depends on reliable access to safe drinking water, but in many developing countries only a limited number of wells and boreholes are available. Many of these water resources are contaminated with biological or chemical pollutants. The goal of this study was to examine water access and quality in urban Bo, Sierra Leone. A health census and community mapping project in one neighborhood in Bo identified the 36 water sources used by the community. A water sample was taken from each water source and tested for a variety of microbiological and physicochemical substances. Only 38.9% of the water sources met World Health Organization (WHO) microbial safety requirements based on fecal coliform levels. Physiochemical analysis indicated that the majority (91.7%) of the water sources met the requirements set by the WHO. In combination, 25% of these water resources met safe drinking water criteria. No variables associated with wells were statistically significant predictors of contamination. This study indicated that fecal contamination is the greatest health risk associated with drinking water. There is a need to raise hygiene awareness and implement inexpensive methods to reduce fecal contamination and improve drinking water safety in Bo, Sierra Leone.     

Reduced analytical availability of polychlorinated biphenyls (PCB's) in colored surface water

It has been generally accepted, during the last few decades, that the dissolved natural organic matter in water [DNOM] appearing as yellow brownish color, has become more and more "polluted" by inorganic and organic micro-pollutants. Due to the complexing properties of NOM, lipophilic organic micro-pollutants, such as, PCBs will be mobilized into water together with the DNOM. A mixture of eight PCBs, with Cl-content from tri-Cl to hepta-Cl, was added to solutions of ten different DNOMs. The DNOMs were aqua's solutions of RO-(reverse osmosis)-isolated material, having approximately the same concentration of carbon. After a contact time of three days, standard analytical PCB-method was used to determine the recovery of the added PCBs. The results show that the analytical availability of the added PCB was significantly reduced in the presence DNOM, compared to distilled water. The percentage loss in recovery of PCB increased with the content of Cl, in mean, from 3%/mg C for tri-Cl to 9%/mg C for hepta-Cl. The results also suggest that the analytical recovery of PCB was affected by the quality and the nature of the organic matter. For example the longer the DNOMs had been in the aquatic phase, the less efficient they are attached to the PCBs.     

Residences with anomalous soil concentrations of dioxin-like compounds in two communities in Michigan, USA: a case study

Most contamination of residential property soil with dioxin-like compounds occurs as a result of proximity to industrial activity that produces such compounds and, outside the industrially impacted zone, the soil concentrations are at background levels. However, as part of the University of Michigan Dioxin Exposure Study, residential properties in the lower peninsula of Michigan, USA, were identified that were located far enough from known sources of these compounds that the soil concentrations should have been at background levels and yet the toxic equivalent (TEQ) of some properties' soil was greater than 2.5 standard deviations above the mean background level. In the three cases presented here from Midland/Saginaw Counties, the anomalously high-TEQ values were primarily due to the presence of polychlorinated dibenzofurans. Based on interviews with the residents and a comparison of soil congener profiles, it was deduced that these values resulted from anthropogenic soil movement from historically contaminated areas. In the cases from Jackson/Calhoun Counties, the unusually high-TEQ values were primarily due to polychlorinated biphenyls. In the case profiled here, it appears that the soil became contaminated through sandblasting to remove paint from the swimming pool. This study identified two mechanisms for soil contamination outside zones of industrial impact; thus, an assumption of background levels of soil contamination outside industrial zones may not be valid.