Mapping the noise in a Greek general hospital.

Sound pressure levels were monitored in a general hospital, in Greece, at ten indoor locations and at three outdoor locations, in the yard of the building. The selected indoor locations are representative of distinct activities that are common in every hospital, such as the emergency department, patient wards and several supporting services, like washing the clothes or the dishes. Noise levels were highly variable in each monitoring location and depended on the activities in the room, such as conversations, medical equipment in use, analytical devices or other machinery in operation. The highest noise levels that were recorded were in the blood donation unit and in the laundry room (the L10,8h was 73 and 79 dB(A) respectively), mainly due to the opening/closing of the metal lids of garbage bins in the first location and due to the wringing of the clothes in the second. Indoor background noise levels i.e. the L95,8h values, were more than 55 dB(A) and higher than the respective outdoor values (except of the L95,8h in one ward of the paediatric ward). The calculated average LEX, 8h was 69.3 dB(A), below the European Union lower exposure action limit value, i.e. 87 dB(A), that was set to prevent hearing loss of the employees. However, noise levels in the wards, in the emergency and the outpatient department were above the values suggested by international guidelines for a healing environment. Sound spectra revealed peaks in frequencies that were representative of the sources of the noise and also the presence of low frequency noise components.

Indoor and outdoor elemental mercury: a comparison of three different cases.

Gaseous elemental mercury (GEM) concentrations were determined in three different indoor environments: an office in a building with no indoor sources of mercury (Bldg. I), an office affected by indoor mercury emissions from an adjacent laboratory (Bldg. II), and finally, an office where an outdoor mercury spill occurred accidentally (Bldg. III). The maximum recorded indoor GEM concentrations, with the largest variation in time, were observed in Bldg. II, with a continuous indoor mercury source (lower to upper quartile 15 to 62 ng m-3). The lowest values were recorded in Bldg. I (lower to upper quartile 3 to 5 ng m-3), where indoor GEM levels were affected mainly by the exhaust of vehicles in the parking lot of the building. The monitoring of GEM indoors (lower to upper quartile 15 to 42 ng m-3), and outdoors (in several heights) of the Bldg. III, revealed that the cleaning up procedure that followed the spill was not adequate. Auxiliary measurements in the first two cases were the indoor microclimatic conditions, as well as the indoor CO2 concentrations, and in the third case the outdoor meteorological data. The exhaust of vehicles, the chemical reagents, and an outdoor mercury spill were found to mainly affect the observed indoor GEM levels. People in Bldg. II and people walking through the area, where Hg0 was spilled, were found to be exposed to concentrations above some guide values.

Energy flux parametrization as an opportunity to get Urban Heat Island insights: The case of Athens, Greece (Thermopolis 2009 Campaign).

Energy flux parameterization was effected for the city of Athens, Greece, by utilizing two approaches, the Local-Scale Urban Meteorological Parameterization Scheme (LUMPS) and the Bulk Approach (BA). In situ acquired data are used to validate the algorithms of these schemes and derive coefficients applicable to the study area. Model results from these corrected algorithms are compared with literature results for coefficients applicable to other cities and their varying construction materials. Asphalt and concrete surfaces, canyons and anthropogenic heat releases were found to be the key characteristics of the city center that sustain the elevated surface and air temperatures, under hot, sunny and dry weather, during the Mediterranean summer. A relationship between storage heat flux plus anthropogenic energy flux and temperatures (surface and lower atmosphere) is presented, that results in understanding of the interplay between temperatures, anthropogenic energy releases and the city characteristics under the Urban Heat Island conditions.

A study of the hourly variability of the urban heat island effect in the Greater Athens Area during summer.

Measurements of air temperature and humidity in the urban canopy layer during July 2009 in 26 sites in Athens, Greece, allowed for the mapping of the hourly spatiotemporal evolution of the urban heat island (UHI) effect. City districts neighboring to the mountains to the east were the hottest during the afternoon, while being among the coolest during the early morning hours. While during the early morning some coastal sites were the hottest, the warm air plume slowly moved to the densely urbanized center of the city until 14:00-15:00, moving then further west, to the Elefsis industrial area in the afternoon. Results from the UrbClim model agree fairly well with the observations. Satellite-derived land surface temperature (LST) data from AATSR, ASTER, AVHRR and MODIS, for pixels corresponding to ground stations measuring Tair, showed that LST can be up to 5K lower than the respective Tair during nighttime, while it can be up to 15K higher during the rest of the day. Generally, LST during late afternoon as acquired from AATSR is very near to Tair for all stations and all days, i.e., the AATSR LST afternoon retrieval can be used as a very good approximation of Tair. The hourly evolution of the spatial Tair distribution was almost the same during days with NE Etesian flow as in days with sea breeze circulation, indicating that the mean wind flow was not the main factor controlling the diurnal UHI evolution, although it influenced the temperatures attained. No unambiguous observation of the urban moisture excess (UME) phenomenon could be made.

Severe particulate pollution from the deposition practices of the primary materials of a cement plant.

Global cement production has increased twofold during the last decade. This increase has been accompanied by the installation of many new plants, especially in Southeast Asia. Although various aspects of pollution related to cement production have been reported, the impact of primary material deposition practices on ambient air quality has not yet been studied. In this study, we show that deposition practices can have a very serious impact on levels of ambient aerosols, far larger than other cement production-related impacts. Analyses of ambient particulates sampled near a cement plant show 1.3-30.4 mg/m(3) total suspended particulates in the air and concentrations of particles with a diameter of 10 µm or less at 0.04-3 mg/m(3). These concentrations are very high and seriously exceed air quality standards. We unequivocally attribute these levels to outdoor deposition of cement primary materials, especially clinker, using scanning electron microscopy/energy-dispersive X-ray spectroscopy. We also used satellite-derived aerosol optical depth maps over the area of study to estimate the extent of the spatial impact. The satellite data indicate a 33% decrease in aerosol optical depth during a 10-year period, possibly due to changing primary material deposition practices. Although the in situ sampling was performed in one location, primary materials used in cement production are common in all parts of the world and have not changed significantly over the last decades. Hence, the results reported here demonstrate the dominant impact of deposition practices on aerosol levels near cement plants.

Polycyclic aromatic hydrocarbons and their oxygenated derivatives in the urban atmosphere of Athens.

Ambient samples of coarse and fine organic particulate matter collected from two urban sites in the city of Athens over one warm and one cold period have been solvent-extracted and quantitatively characterized by gas chromatography-mass spectrometry for their content of polycyclic aromatic hydrocarbons (PAHs) and oxidized PAHs (oxyPAHs). Variable concentrations were observed for the two distinct monthly periods representing a cold, dry period and a summer period, relating to strong local primary emissions and to lower emissions with more stable meteorological conditions, respectively. Additionally, gaseous concentrations of selected PAHs were calculated, revealing that the relative proportions between gaseous and particle phase of individual compounds may differ significantly between summer and late winter, reflecting changes in PAH emission sources and climate conditions. In fact almost all of SigmaPAHs were attributed to combustion sources (82-92%), while more than half are considered as comprising of probable human carcinogens (47-62%). Traffic was confirmed as the major contributor of PAHs when appropriate diagnostic ratios and traffic marker compounds were used. This approach also led to the estimation of diesel versus petrol contribution to the atmospheric PAH burden, using the methylphenanthrene to phenanthrene ratio. The fourteen oxygenated polycyclic compounds that were quantified had greater concentrations in the colder period. Among these compounds 9,10-phenanthrenequinone, 1-pyrenecarboxaldehyde and 9H-fluoren-9-one had the highest concentrations.

Origins of n-alkanes, carbonyl compounds and molecular biomarkers in atmospheric fine and coarse particles of Athens, Greece.

The abundance and origin of aliphatic hydrocarbons, carbonyl compounds and molecular biomarkers found in the aliphatic fraction of PM(10-2.5) and PM(2.5) in the centre of Athens Greece are discussed in an attempt to reveal seasonal air pollution characteristics of the conurbation. Each extract was fractionated into individual compound classes and was analyzed using gas chromatography coupled to mass spectrometry. Normal alkanes, ranging from C(14) to C(35), were abundant in PM(10-2.5) and PM(2.5) samples during both sampling campaigns. The daily concentration of total n-alkanes was up to 438 ng m(-3) for PM(10-2.5) and up to 511 ng m(-3) for PM(2.5). Additionally, gaseous concentrations of n-alkanes were calculated, revealing that the relative proportions between gaseous and particle phases of individual compounds may differ significantly between summer and late winter. Normal alkanals and alkan-2-ones were only detected in the fine fraction of particulate matter and their concentrations were much lower than the n-alkane concentrations. Several geochemical parameters were used to qualitatively reconcile the sources of organic aerosol. The carbon preference index (CPI) of the coarse particles in August had the highest value, while in March the leaf wax contribution decreased significantly and the CPI value was very close to unity for both sites. Maximum concentrations of carbonyl compounds were reported in the range of C(15)-C(20), demonstrating that they were formed from anthropogenic activity or from atmospheric oxidative processes. 6, 10, 14-trimethylpentadecan-2-one, a marker of biogenic input, was also detected in our samples. Molecular biomarker compounds confirmed that ca. 60% of the aliphatic fraction on the sampled atmospheric particles originated from petroleum and not from any contemporary biogenic sources. Pristane and phytane were detected in the fine fraction with their presence indicating sources of fossil fuel in the range of C(16)-C(20). At all sites the 17alpha(Eta),21beta(Eta) hopane series was the most abundant hopane group.

Characterisation of indoor airborne particles by using real-time aerosol mass spectrometry.

An Aerosol Time-of-Flight Mass Spectrometer (ATOFMS; TSI 3800) was deployed to Athens (Greece) during August 2003. The instrument provides information on a polydisperse aerosol, acquiring precise aerodynamic diameter (+/-1%) within the range 0.3 to 3 mum and individual particle positive and negative mass spectral data in real time. Sampling was carried out indoors and outdoors at an office in a building on a minor road in the city centre and various outdoor and indoor sources were identified. Specific outdoor particles such as dust and carbon particles were detected in indoor air. The generation of particles from indoor sources was studied and several different types of particle were found to be present in environmental tobacco smoke (ETS): three were potassium-rich (with differing proportions of carbon) emitted directly in the exhaled mainstream smoke. Two other types arose mainly when the cigarette was left smouldering on an ash-tray. Another particle type exhibited a strong signal at m/z 84, most likely due to a nicotine fragment. The temporal trend of this specific particle type showed likely condensation of semi-volatile constituents on existing potassium-rich particles. A release of insect repellent in the room was also successfully monitored.

Transport of toxic organic aerosol pollutants from Yugoslavia to Greece during the operation "Allied Force".

Between March 24 and June 10, 1999 a large number of chemicals were ejected into the atmosphere because of air strikes on chemical industries and oil storage facilities in former Yugoslavia. Chemicals released into the atmosphere under suitable meteorological conditions can be transported across borders to large distances. The releases may have contained not only conventional air pollutants but also semi-volatile organic compounds (SOCs) which include dioxins, furans, PCBs and PAHs, all known to be hazardous to health. A measuring programme was initiated at Democritus University Thrace, Greece to monitor the chemical characteristics of atmospheric aerosol during February, March and April 1999. Particulate matter (aerosol) was collected on filters and was analysed using high-resolution gas chromatography coupled to high-resolution mass spectrometry for their content in SOCs. In the present work we show evidence of two events with three to twenty fold increased SOCs in the atmosphere of Northern Greece which were associated with air masses transported from the conflict area, following the destruction of chemical plants and oil storage facilities.

The war in Kosovo: Evidence of pollution transport in the Balkans during operation "Allied Force".

During the operation "Allied Force" in the spring of 1999, the burning or damaging of industrial and military targets in the Former Republic of Yugoslavia resulted in the release of a large number of chemicals into the atmosphere. The releases contained not only conventional air pollutants, but also Semi-Volatile Organic compounds (SVOs) which are known to be hazardous to health. Under suitable meteorological conditions, these chemicals can be transported across borders over large distances. In this paper, an analysis of measurements and dispersion calculations is presented which provides evidence of pollutant transport from the conflict area to Greece. The measuring program was carried out in Xanthi, Greece and included aerosol sampling and subsequent analysis for the determination of the concentration of SVOs including dioxins, furans, PCBs (PolyChlorinated Biphenyls), PAHs (Polycyclic Aromatic Hydrocarbons) and organic phthalates. This paper focuses on two episodes of organic phthalates that were observed during the conflict period. Pollution measurements are interpreted by means of air trajectories and dispersion calculations. For this purpose, the HYSPLIT_4 (HYbrid Single-Particle Langrangian Integrated Trajectory) modeling system is used to calculate the dispersion of toxic substances.

Greenhouse gases in cold water filaments in the arabian sea during the southwest monsoon

The distribution of partial pressure of carbon dioxide and the concentrations of nitrous oxide and methane were investigated in a cold water filament near the coastal upwelling region off Oman at the beginning of the southwest monsoon in 1997. The results suggest that such filaments are regions of intense biogeochemical activity which may affect the marine cycling of climatically relevant trace gases.http://link.springer. de/link/service/journals/00114/bibs/9086010/90860489.htm

Determination of butyltin compounds in sediments using an improved aqueous ethylation method.

We have determined tributyltin and dibutyltin species in various environmental sediment samples (marine, harbour and river sediment) using the in situ aqueous ethylation-gas chromatography-atomic absorption spectrometry method subsequent to extraction by methanol containing O.5M HCl. The present technique provides a significantly lower detection limit than previous methods, so that tributyltin can for the first time be measured in some of the samples. Thus, the method described is well suited for the determination of tributyltin and dibutyltin compounds in sediments with low levels of butyltin species (e.g., Main River, 1.7 ng of tributyltin as Sn/g dry sediment).

Determination of methylmercury in fish samples using GC/AA and sodium tetraethylborate derivatization.

A simple technique is described for the rapid determination of methylmercury in fish tissue. Following simple dissolution in methanolic KOH solution, aqueous phase ethylation by derivatization with NaB(C2H5)4, cryogenic trapping on a packed chromatographic column, and GC separation, volatile mercury species are detected by atomic absorption spectrometry. Absolute detection limits are 4 pg of Hg for CH3Hg+ and 75 pg of Hg for labile Hg2+. Concentration detection limits for this optimized procedure are 4 ng of Hg for CH3Hg+ and 75 ng of Hg for labile Hg2+ per gram of pulverized dried fish tissue. Analysis of standard reference materials demonstrates the accuracy, precision, and reproducibility of the analytical method.