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PM 2.5 (i.e., particles with aerodynamic diameters less than 2.5 μm) and the associated water-soluble, dissolved, and labile fractions of heavy metals (Cu, Pb, Mn, Ni, Co, Zn, Cr, and Cd) were determined in indoor air of twenty workplaces in Alexandroupolis (Northeastern Greece). PM 2.5 concentrations exhibited significant variance across the workplaces ranging from 11.5 μg m -3 up to 276 μg m -3 . The water-soluble metal concentrations varied between 0.67 ± 2.52 ng m -3 for Co and 27.8 ± 19.1 ng m -3 for Ni exhibiting large variations among the different workplaces. The water-soluble metal fractions were further treated to obtain the labile metal fraction (by binding with Chelex 100-chelating resin) that might represent a higher potential for bioaccessibility than the total water-soluble fraction. The largest labile (chelexed) fractions (48-67% of the corresponding water-soluble concentrations) were found for Cd, Mn, Cu, and Ni, while the labile fractions of Pb, Cr, Co, and Zn were relatively lower (34-42% of the corresponding water-soluble concentrations). Water-soluble and labile concentrations of heavy metals were further used to calculate cancer and non-cancer risks via inhalation of the PM 2.5 -bound metals. To our knowledge, this is the first study estimating the health risks due to the inhalation of water-soluble and labile metal fractions bound to indoor PM., (© 2020. Springer-Verlag GmbH Germany, part of Springer Nature.)

A yearlong study of odor-active VOCs was carried out in the northwestern district of the city of Thessaloniki, Greece, which is in close vicinity to a large-scale petroleum refining and petrochemical process complex, as well as other activities such as power generation from natural gas burning and liquefied petroleum gas (LPG) shipping. Odor nuisance has been a major concern in the district often rising complaints from local residents. A total of 312 samples of VOCs were collected at three sites during a 12-month period (May 2018-May 2019) on thermal desorption cartridges and analyzed by thermal desorption gas chromatography interfaced with mass selective detector (TD-CG/MS). Fifty-five odorous compounds including 8 mercaptans, 5 thiophenes, 7 sulfides, 22 aromatics, and 13 aldehydes were measured, and their spatial and temporal variations were assessed. Concentrations found were compared with those measured at other sites within the urban agglomeration Thessaloniki. Correlations with meteorological conditions (ambient temperature, relative humidity, wind direction/speed, and frequency/depth of temperature inversions) were investigated. Bivariate polar plots of the concentrations of Σ 8 Mercaptans, Σ 5 Thiophenes, Σ 7 Sulfides, Σ 22 Aromatics, and Σ 13 Aldehydes as a function of wind speed and wind direction were constructed for source localization., (© 2020. Springer-Verlag GmbH Germany, part of Springer Nature.)

Commuters are exposed to high air pollution levels daily, especially in areas with dense traffic. This study examines the commuter's exposure to polycyclic aromatic hydrocarbons (PAHs) in the city of Thessaloniki, Greece, under three different commuting modes: biking, travelling by private car, and riding public transportation means (buses). The study was carried out from 2015 to 2018 including 43 volunteers (15 cyclists, 17 car drivers/passengers, and 11 bus passengers). The personal exposure concentrations to particles smaller than 4-μm aerodynamic diameter (PM 4 ), constituting the respirable fraction of total airborne particles, and the associated PAHs were assessed for each commuting mode during the cold and the warm period of the year. Whereas the exposure of bus and car passengers to in-cabin PM 4 were higher in the cold season, the exposure of cyclists exhibited the opposite seasonality. In all commuting modes, exposure to PAHs was higher in the cold season. In both seasons, exposure concentration followed the order: cyclists > bus passengers > car passengers. The carcinogenic and mutagenic potencies of the exposure PAH concentrations were calculated using Benzo[a]pyrene (BaP) carcinogenic and mutagenic equivalency factors. The inhalation cancer risk (ICR) associated to PAHs was further estimated and compared between the different commuting modes. Our data can provide relevant information for transport decision-making and increase environmental awareness for a more rational approach to urban travelling., (© 2020. Springer-Verlag GmbH Germany, part of Springer Nature.)

The deposition of ambient submicron particles in the different parts of the human respiratory tract (HRT) was, for the first time, estimated for males and females from different age classes (children-adults-seniors) of urban population in the city of Thessaloniki, northern Greece, during the cold and the warm period of the year. Outdoor daily and hourly particle number doses in the different regions of the HRT, i.e., the extra-thoracic (ET), tracheobronchial (TB), and the acinar (AC) regions, were calculated by employing the Multiple-Path Particle Dosimetry (MPPD) model. Because of the absence of information being available for the hygroscopic properties of particles, three different particle hygroscopicity scenarios were considered: (i) non-hygroscopic (i.e., raw model estimations), (ii) nearly hydrophobic, and (iii) hygroscopic particles. When hygroscopic properties were considered, we found a remarkable reduction (up to ~ 55%) in the estimated total particle number doses in comparison to the non-hygroscopic particle scenario. Furthermore, we found that the size distribution pattern of the particle doses within the different parts of the HRT was strongly affected by particles' hygroscopic properties with the non-hygroscopic particle scenario significantly overestimating the particle doses in the sub-100-nm range, while underestimating the doses of larger particles. On the contrary, the deposition density appeared to be negligibly affected by the particles' hygroscopic properties, implying the existence of a possible threshold in the number of particles deposited per airway surface area. Similarly, the lobar particle number deposition fraction was unaffected by the hygroscopic properties of particles, as well as the ambient particle size distribution and the individuals' physiological parameters. The total particle number deposition doses estimated here are within the range of the corresponding values reported for other urban environments. It is hoped that our findings could contribute to better understanding of submicron particle exposure and add to the development of more sufficient methods to evaluate the related health impacts.

Two classes of polar organic compounds, dicarboxylic acids (DCAs) and sugars/sugar anhydrides (S/SAs), were measured in airborne particulate matter in the area of Thessaloniki, northern Greece. The target compounds were measured simultaneously in two particle fractions PM 10 and PM 2.5 during cold and warm periods by employing extraction in an ultrasonic bath with a mixture of MeOH/DCM (1:2 v/v), derivatization with BSTFA-TMCS and GC-MS for analysis. At both fractions, phthalic was the predominant carboxylic acid during cold season and a-ketoglutaric acid in warm season, followed by maleic and malic. Levoglucosan was the dominant sugar anhydride during the cold and arabitol during the warm season. In total, the distribution of DCAs seemed to favor the PM 2.5 particle fraction, probably due to anthropogenic emissions and photochemical formation. The relative contribution of DCAs to PM 2.5 fraction was 0.9-3.2% in cold and 0.9-7.0% in warm period. Regarding S/SAs, levoglucosan was also predominantly distributed in fine particles, with relative contribution to this fraction 0.1-6.3% in cold and <0.65% in warm season, suggesting impact of biomass burning emissions. In contrast, arabitol, fructose, and glucose were mainly found in coarse fraction, possibly due to their biogenic origin. Negative correlation of target compounds with temperature and total solar radiation suggested the contribution of seasonal dependant local sources. Positive relationship with NO and NO 2 oxidants and relative humidity showed secondary formation of polar compounds or enhanced gas-to-particle conversion.

The Western Macedonian Lignite Center (WMLC) in northwestern Greece is the major lignite center in the Balkans feeding four major power plants of total power exceeding 4 GW. Concentrations of PM 10 (i.e., particulate matters with diameters ≤10 μm) are the main concern in the region, and the high levels observed are often attributed to the activities related to power generation. In this study, the contribution of fugitive dust emissions from the opencast lignite mines to the ambient levels of PM 10 in the surroundings was estimated by performing chemical mass balance (CMB) receptor modeling. For this purpose, PM 10 samples were concurrently collected at four receptor sites located in the periphery of the mine area during the cold and the warm periods of the year (November-December 2011 and August-September 2012), and analyzed for a total of 26 macro- and trace elements and ionic species (sulfate, nitrate, chloride). The robotic chemical mass balance (RCMB) model was employed for source identification/apportionment of PM 10 at each receptor site using as inputs the ambient concentrations and the chemical profiles of various sources including the major mine operations, the fly ash escaping the electrostatic filters of the power plants, and other primary and secondary sources. Mean measured PM 10 concentrations at the different sites ranged from 38 to 72 μg m -3 . The estimated total contribution of mines ranged between 9 and 22% in the cold period increasing to 36-42% in the dry warm period. Other significant sources were vehicular traffic, biomass burning, and secondary sulfate and nitrate aerosol. These results imply that more efficient measures to prevent and suppress fugitive dust emissions from the mines are needed.

The occurrence and atmospheric behavior of tri- to deca-polybrominated diphenyl ethers (PBDEs) were investigated during a 2-week campaign concurrently conducted in July 2012 at four background sites around the Aegean Sea. The study focused on the gas/particle (G/P) partitioning at three sites (Ag. Paraskevi/central Greece/suburban, Finokalia/southern Greece/remote coastal, and Urla/Turkey/rural coastal) and on the size distribution at two sites (Neochorouda/northern Greece/rural inland and Finokalia/southern Greece/remote coastal). The lowest mean total (G + P) concentrations of ∑ 7 PBDE (BDE-28, BDE-47, BDE-66, BDE-99, BDE-100, BDE-153, BDE-154) and BDE-209 (0.81 and 0.95 pg m -3 , respectively) were found at the remote site Finokalia. Partitioning coefficients, K P , were calculated, and their linear relationships with ambient temperature and the physicochemical properties of the analyzed PBDE congeners, i.e., the subcooled liquid pressure (P L °) and the octanol-air partition coefficient (K OA ), were investigated. The equilibrium adsorption (P L °-based) and absorption (K OA -based) models, as well as a steady-state absorption model including an equilibrium and a non-equilibrium term, both being functions of log K OA , were used to predict the fraction Φ of PBDEs associated with the particle phase. The steady-state model proved to be superior to predict G/P partitioning of BDE-209. The distribution of particle-bound PBDEs across size fractions < 0.95, 0.95-1.5, 1.5-3.0, 3.0-7.2, and > 7.2 μm indicated a positive correlation between the mass median aerodynamic diameter and log P L ° for the less brominated congeners, whereas a negative correlation was observed for the high brominated congeners. The potential source regions of PBDEs were acknowledged as a combination of long-range transport with short-distance sources.

In this study, we report for the first time particle number doses in different parts of the human respiratory tract and real-time deposition rates for particles in the 10 nm to 10 μm size range emitted by digital printing operations. Particle number concentrations (PNCs) and size distribution were measured in a typical small-sized printing house using a NanoScan scanning mobility particle sizer and an optical particle sizer. Particle doses in human lung were estimated applying a multiple-path particle dosimetry model under two different breathing scenarios. PNC was dominated by the ultrafine particle fractions (UFPs, i.e., particles smaller than 100 nm) exhibiting almost nine times higher levels in comparison to the background values. The average deposition rate fοr each scenario in the whole lung was estimated at 2.0 and 2.9 × 10 7 particles min -1 , while the respective highest particle dose in the tracheobronchial tree (2.0 and 2.9 × 10 9 particles) was found for diameter of 50 nm. The majority of particles appeared to deposit in the acinar region and most of them were in the UFP size range. For both scenarios, the maximum deposition density (9.5 × 10 7 and 1.5 × 10 8 particles cm -2 ) was observed at the lobar bronchi. Overall, the differences in the estimated particle doses between the two scenarios were 30-40% for both size ranges.

Thirteen particle-phase PAHs, including nine >4-ring congeners [Benz[a]anthracene (BaAn), Chrysene (Chry), Benzo[b]fluoranthene (BbF), Benzo[k]fluoranthene (BkF), Benzo[e]pyrene (BeP), Benzo[a]pyrene (BaP), Dibenzo[a,h]anthracene (dBaAn), Benzo[g,h,i]perylene (BghiPe), Indeno(1,2,3-c,d)pyrene (IP)], listed by IARC (International Agency for Research on Cancer) as class 1, class 2A, and 2B carcinogens, plus four ≤ 4-ring congeners [Phenanthrene (Ph), Anthracene (An), Fluoranthene (Fl), Pyrene (Py)], were concurrently measured in inhalable and respirable particle fractions (PM10 and PM2.5) at a heavy-traffic and an urban background site in Thessaloniki, northern Greece, during the warm and the cold period of the year. Carcinogenic and mutagenic potencies of the PAH-bearing particles were calculated, and the inhalation cancer risk (ICR) for local population was estimated. Finally, Chemical Mass Balance (CMB) modeling was employed for the source apportionment of ambient PAH levels and the estimated lung cancer risk. Resulted inhalation cancer risk during winter was found to be equivalent in the city center and the urban background area suggesting that residential wood burning may offset the benefits from minor traffic emissions.

Near-ground air (26 substances) and surface seawater (55 substances) concentrations of persistent toxic substances (PTS) were determined in July 2012 in a coordinated and coherent way around the Aegean Sea based on passive air (10 sites in 5 areas) and water (4 sites in 2 areas) sampling. The direction of air-sea exchange was determined for 18 PTS. Identical samplers were deployed at all sites and were analysed at one laboratory. hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs) as well as dichlorodiphenyltrichloroethane (DDT) and its degradation products are evenly distributed in the air of the whole region. Air concentrations of p,p'-dichlorodiphenyldichloroethylene (p,p'-DDE) and o,p'-DDT and seawater concentrations of p,p'-DDE and p,p'-DDD were elevated in Thermaikos Gulf, northwestern Aegean Sea. The polychlorinated biphenyl (PCB) congener pattern in air is identical throughout the region, while polybrominated diphenylether (PBDE)patterns are obviously dissimilar between Greece and Turkey. Various pollutants, polycyclic aromatic hydrocarbons (PAHs), PCBs, DDE, and penta- and hexachlorobenzene are found close to phase equilibrium or net-volatilisational (upward flux), similarly at a remote site (on Crete) and in the more polluted Thermaikos Gulf. The results suggest that effective passive air sampling volumes may not be representative across sites when PAHs significantly partitioning to the particulate phase are included.

Mercury (Hg) is a toxic element that is emitted to the atmosphere through human activities, mainly fossil fuel combustion. Hg accumulations in soil are associated with atmospheric deposition, while coal-burning power plants remain the most important source of anthropogenic mercury emissions. In this study, we analyzed the Hg concentration in the topsoil of the Kozani-Ptolemais basin where four coal-fired power plants (4,065 MW) run to provide 50 % of electricity in Greece. The study aimed to investigate the extent of soil contamination by Hg using geostatistical techniques to evaluate the presumed Hg enrichment around the four power plants. Hg variability in agricultural soils was evaluated using 276 soil samples from 92 locations covering an area of 1,000 km(2). We were surprised to find a low Hg content in soil (range 1-59 μg kg(-1)) and 50 % of samples with a concentration lower than 6 μg kg(-1). The influence of mercury emissions from the four coal-fired power plants on soil was poor or virtually nil. We associate this effect with low Hg contents in the coal (1.5-24.5 μg kg(-1)) used in the combustion of these power plants (one of the most Hg-poor in the world). Despite anthropic activity in the area, we conclude that Hg content in the agricultural soils of the Kozani-Ptolemais basin is present in low concentrations.

Concentrations and chemical composition of the coarse particle fraction (PMc) were investigated at two urban sites in the city of Thessaloniki, Greece, through concurrent sampling of PM10 and PM2.5 during the warm and the cold months of the year. PMc levels at the urban-traffic site (UT) were among the highest found in literature worldwide exhibiting higher values in the cold period. PMc levels at the urban-background site (UB) were significantly lower exhibiting a reverse seasonal trend. Concentration levels of minerals and most trace metals were also higher at the UT site suggesting a stronger impact from traffic-related sources (road dust resuspension, brake and tire abrasion, road wear). According to the chemical mass closure obtained, minerals (oxides of Si, Al, Ca, Mg, Fe, Ti, and K) dominated the PMc profile, regardless of the site and the period, with organic matter and secondary inorganic aerosols (mainly nitrate) also contributing considerably to the PMc mass, particularly in the warm period. The influence of wind speed to dilution and/or resuspension of coarse particles was investigated. The source of origin of coarse particles was also investigated using surface wind data and atmospheric back-trajectory modeling. Finally, the contribution of resuspension to PMc levels was estimated for air quality management perspectives.

Organic carbon (OC) and elemental carbon (EC) concentrations, associated to PM10 and PM2.5 particle fractions, were concurrently determined during the warm and the cold months of the year (July-September 2011 and February-April 2012, respectively) at two urban sites in the city of Thessaloniki, northern Greece, an urban-traffic site (UT) and an urban-background site (UB). Concentrations at the UT site (11.3 ± 5.0 and 8.44 ± 4.08 14 μg m(-3) for OC10 and OC2.5 vs. 6.56 ± 2.14 and 5.29 ± 1.54 μg m(-3) for EC10 and EC2.5) were among the highest values reported for urban sites in European cities. Significantly lower concentrations were found at the UB site for both carbonaceous species, particularly for EC (6.62 ± 4.59 and 5.72 ± 4.36 μg m(-3) for OC10 and OC2.5 vs. 0.93 ± 0.61 and 0.69 ± 0.39 μg m(-3) for EC10 and EC2.5). Despite that, a negative UT-UB increment was frequently evidenced for OC2.5 and PM2.5 in the cold months possibly indicative of emissions from residential wood burning at the urban-background site. At both sites, cconcentrations of OC fractions were significantly higher in the cold months; on the contrary, EC fractions at the UT site were prominent in the warm season suggesting some influence from maritime emissions in the nearby harbor area. Secondary organic carbon, being estimated using the EC tracer method and seasonally minimum OC/EC ratios, was found to be an appreciable component of particle mass particularly in the cold season. The calculated secondary contributions to OC ranged between 35 and 59 % in the PM10 fraction, with relatively higher values in the PM2.5 fraction (39-61 %). The source origin of carbonaceous species was investigated by means of air parcel back trajectories, satellite fire maps, and concentration roses. A local origin was mainly concluded for OC and EC with limited possibility for long range transport of biomass (agricultural waste) burning aerosol.

Goal, Scope and Background: Dissolved organic carbon (DOC) constitutes a parameter of organic pollution for waters and wastewaters, which is not so often studied, and it is not yet regulated by directives. The term 'DOC' is used for the fraction of organics that pass through a 0.45 microm pores' size membrane. The type of wastewater plays an important role in the quality of DOC and it has been shown that DOC may contain aquatic humic substances, hydrophobic bases, hydrophobic neutrals, hydrophilic acids, hydrophilic bases and hydrophilic neutrals. The quality of the DOC is expected to affect its fate in a wastewater treatment plant (WWTP), since a considerable fraction of DOC is not biodegradable, and it may be released in the aquatic environment together with the treated effluent. In the present study, the occurrence of DOC during the wastewater treatment process is investigated and its removal rates during primary, secondary and overall treatment are being estimated. Furthermore, a correlation is being attempted between DOC and the concentrations of selected Persistent Organic Pollutants (POPs) and Heavy Metals (HMs) in the dissolved phase of wastewaters, to examine whether there are common sources for these pollution parameters in WWTPs. Also, DOC is being correlated with the partition coefficients of the above-mentioned pollutants in wastewater, in order to examine the effect of 'solubility enhancement' in WWTPs and to evaluate the result of this phenomenon in the efficiency of a WWTP to remove organic pollutants., Methods: For the purposes of this study, 24-h composite wastewater samples were collected from the influent (raw wastewater, RW), the effluent of primary sedimentation tank (primary sedimentation effluent, PSE) and the effluent of secondary sedimentation tank (secondary sedimentation effluent, SSE). Samples were analyzed for the presence of 26 POPs (7 PCBs and 19 organochlorine pesticides), 8 HMs and DOC., Results and Discussion: Mean concentrations of DOC in RW and PSE were at similar levels (approximately 70 mg l(-1)), suggesting that primary treatment has a minor effect on the DOC content of wastewater. DOC concentrations in SSE were significantly lower (approximately 19 mg l(-1)) as a result of the degradation of organic compounds in the biological reactor. Calculated removals of DOC were 0.8% in the primary treatment, 63% in the secondary treatment, and 69% in the overall treatment, exhibiting large differences from other organic pollution parameters, such as BOD and COD. The overall DOC removal was found to be independent from the DOC concentration in raw wastewater. Poor correlation was also observed between the DOC content and the concentrations of wastewater contaminants, such as persistent organic pollutants (POPs) and heavy metals (HMs), probably suggesting that their occurrence in WWTPs is due to different sources. A good negative linear relationship was revealed between DOC concentrations and the logarithms of the distribution coefficients (Kd) of various POPs and HMs between the solid and the liquid phases of wastewater. This relationship suggests that DOC facilitates hydrophobic pollutants to remain in the dissolved phase thus causing lower removal percentages during the treatment process., Conclusion: DOC was measured at three stages of a municipal WWTP that receives mainly domestic wastewater and urban runoff. DOC concentrations in untreated and primarily treated wastewater were almost equal, and only after the secondary sedimentation there was a decrease. Concentrations and removal rates of DOC were in the same levels as in other WWTPs that receive municipal wastewater. The origin of DOC was found to be different to the one of POPs and of HMs, as no correlation was observed between the concentrations of DOC and the concentrations of these pollutants. On the contrary, DOC was found to have significant negative correlation with the Kd of all pollutants examined, suggesting that it plays an important role in the partitioning of those pollutants between the dissolved and the sorbed phase of wastewaters. This effect of DOC on partitioning can affect the ability of WWTPs to remove toxic pollutants, and that way it facilitates the discharge of those chemicals in the aquatic ecosystems together with the treated effluent. RRECOMMENDATION:By the results of this work it is shown that the presence of DOC in wastewaters can significantly affect the partition of hazardous pollutants between the dissolved and the sorbed phase. It is therefore of importance that this parameter is controlled more in wastewaters, since it can cause a decrease in the efficiency of WWTPs to remove quantitatively persistent pollutants.

Unlabelled: GOAL, SCOPE, BACKGROUND: Shallow lakes display a number of features that set them apart from the more frequently studied deeper systems. The majority of lakes in Northern Greece are small to moderate in size with a relatively low depth and are considered as sites of high value of the wetland habitat. However, the water quality of these lakes has only been evaluated segmentally and occasionally., Objective: The objectives of this study were to thoroughly investigate nitrogen and phosphorus speciation in lakes of a high ecological significance located in N. Greece, in order to evaluate their eutrophication status and possible nutrient limitation factors, and to investigate the main factors/sources that affect the water quality of these systems., Methods: An extensive survey was carried out during the period from 1998-1999. Water samples were collected on a monthly basis from lakes Koronia, Volvi, Doirani, Mikri Prespa and Megali Prespa located in N. Greece. Water quality parameters (temperature, dissolved oxygen, pH and conductivity), organic indices (COD, BOD5), and N- and P-species (NO3(-), NO2(-), NH4(+), and PO4(3-), Kieldahl nitrogen and acid-hydrolysable phosphorus) were determined according to standard methods for surface water. Statistical treatment of the data was employed., Results and Conclusions: The physicochemical parameters determined in the lakes studied revealed a high temporal variation. The trophic state of the lakes ranged from meso- to hypertrophic. The nutrient limiting factor varied among lakes suggesting either P-limitation conditions or mixed conditions changing from P- to N-limitation throughout the year. Urban/industrial activities and agricultural runoff are the major factors affecting all lakes, although with a varying contribution., Recommendation and Outlook: This lake-specific research offers valuable information about water quality and nutrient dynamics in lakes of significant ecological value located in N. Greece that can be useful for an effective pollution control/management of these systems. Due to the large intra-annual variability of certain physicochemical parameters, a properly designed monitoring program of lake water is recommended.

The recovery of polycyclic aromatic hydrocarbons (PAHs) from lignite coal burnt in Greek power stations and the fly ash produced is examined comparatively using Soxhlet, ultrasonic and accelerated solvent extraction procedures with various organic solvents. Soxhlet using toluene/methanol mixture and accelerated solvent extraction/toluene were found to be the most efficient methods for fly ash PAHs, yielding average recoveries of about 80%. The accelerated solvent extraction/toluene procedure was superior for lignite PAHs, yielding 96% average recovery, whereas ultrasonic and Soxhlet extraction yielded relatively lower recoveries (75% and 67%, respectively).