Assessment of sources and pollution state of trace and toxic elements in street dust in a metropolitan city.

Street dust and urban soil samples are significant part of environmental compartments to evaluate the contamination levels in urban and industrial zones. This study was carried out to ascertain the concentrations of trace and toxic elements in Izmir street dusts collected from 20 different sites dominating by industrial (four sites), residential (seven sites) and traffic (nine sites) areas, and also to figure out the exposure of adults and children to the elemental toxicity in dust. In order to measure the total and soluble concentrations of elements, the dust samples were analyzed with ICP-MS methodology. The results indicated that concentrations of anthropogenic-based elements are homogenously spread out in whole Izmir city in a similar way to crustal-based elements. This indicates that traffic and residential heating were dominant pollutant sources throughout the city dusts. The health risk assessment showed that elemental non-carcinogenic risks are lower than limit value. However, the cancer risks exceed the acceptable level for As and Cr. According to source apportionment analysis, seven factors were defined for trace elements for all site data.

Assessment of seasonal and spatial variations of physicochemical parameters and trace elements along a heavily polluted effluent-dominated stream.

This study focuses on a heavily polluted effluent-dominated stream that passes through an industrialized region near Izmir, Turkey. The intermittent creek receives domestic and industrial discharges of Kemalpasa District Center and its neighborhoods and more than 180 factories of the organized industrial zone. A monitoring campaign was conducted on the creek and samples were taken in two different seasons with distinct hydrological characteristics from 20 stations along the creek to quantify the quality status of water and sediment columns. A number of physicochemical parameters, heavy metals, and trace elements were measured by field and laboratory techniques to assess the status of creek's water and sediment quality. The spatial and temporal variations were determined, and statistical tools were used to conduct an environmental forensic overview along the creek. A geo-accumulation index and a modified heavy metal pollution index were calculated to cumulatively assess the quality of sediment and water columns, respectively. The results revealed that the creek was under significant pollution load from the industrial zone where metal processing, food and beverage production, marble and natural stone manufacturing, and paper production are made. In particular, elements such as Co, Cu, Cd, Mn, Ni, Pb, Zn, and Zr were found to be above the surface water quality standard values. Similarly, B, Cr, Ni, Cu, Zn, and Sn were determined to be in extreme levels in the sediment column with values exceeding the probable effect concentrations.

Biomonitoring the spatial and historical variations of persistent organic pollutants (POPs) in an industrial region.

Several persistent organic pollutants (POPs) like polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs), and polybrominated diphenyl ethers (PBDEs) were measured in needle, branch, bark, and tree ring samples in pine samples collected at 27 sites (21 industrial, 6 background) in Aliaga industrial region in Turkey. Soil, litter, and air samples were also collected to investigate the relationships between the air and soil, litter, and tree components. Concentrations decreased with distance from the sources and the lowest ones were measured at background sites. The spatial distribution of POPs indicated that the major sources in the region are the iron-steel, ship-breaking, petrochemical plants and the petroleum refinery. Significant correlations between the air concentrations and, soil, litter, and tree components indicated the interaction of these compartments with air. Observed increasing trends of POPs in the tree-ring samples were representative for the variations in anthropogenic emissions and resulting atmospheric concentrations in Aliaga region. These results indicated that tree components, litter and soil could be used to determine the spatial variations while tree rings could be used to investigate the historical trends of atmospheric POPs in a region. POP amounts (mg/ha) stored in different tree components, litter, and soil were also inventoried. Among the tree components, generally, the highest amounts were stored in the stem followed by needles. For the overall inventory, the highest amounts were stored in soil for PCNs, PBDEs, and PCBs while highest PAH amounts were stored in trees, indicating that in addition to soil, vegetation is also an important reservoir for POPs.

Spatial distribution and source identification of trace elements in topsoil from heavily industrialized region, Aliaga, Turkey.

Topsoil samples (n = 40) were collected from a heavily industrialized region in Turkey. The region includes several scrap processing iron-steel plants with electric arc furnaces (EAFs), a petroleum refinery, a petrochemical complex, steel rolling mills, a natural gas-fired power plant, ship-breaking yards and very dense transportation activities. The region has undergone a rapid transition from an agricultural region to a heavily industrialized region in the last three decades. Collected soil samples were analyzed for 48 trace elements using inductively coupled plasma-mass spectrometry (ICP-MS). The elemental distribution pattern in the region indicated that Nemrut area with dense iron-steel production activities was a hotspot for elemental pollution. In addition to crustal elements, concentrations of anthropogenic trace elements (i.e., Fe, Zn, Pb, Mn, Cu, Cd, Cr and Mo) were very high in the area influencing many parts of the region. Elemental compositions of fugitive sources polluting the soil (i.e., paved and unpaved roads, slag piles, EAFs filter dust piles and coal piles) were also determined. The methods (enrichment factors [EFs] and the index of geoaccumulation [Igeo]) used for determination of pollution status of soil showed that Cr, Ag, Zn, As and Pb were the strongly contaminating elements for the region. Principal component analysis (PCA) clearly indicated that anthropogenic sources (steel production, refinery and petrochemical processes and traffic) were important sources in this region.

Informal E -waste recycling in nine cities of Pakistan reveals significant impacts on local air and soil quality and associated health risks.

The global increase in electronic waste (e-waste) has led to a rise in informal recycling, emitting hazardous heavy metals (HMs) that threaten human health and ecosystems. This study presents the first comprehensive assessment of HM levels in dry deposition and soils at proximity of forty (40) informal e-waste recycling sites across Pakistan, between September 2020 to December 2021. Findings reveal that Zn (1410), Pb (410) and Mn (231) exhibited the higher mean deposition fluxes (µg/m2.day), derived from air samples, particularly in Karachi. Similarly, soils showed higher mean concentrations (µg/g dw) of Mn (477), Cu (514) and Pb (172) in Faisalabad, Lahore, and Karachi, respectively. HMs concentrations were found higher in winter or autumn and lower in summer. In addition, HM levels were significantly (p = 0.05) higher at recycling sites compared to background sites year-round, highlighting the e-waste recycling operations as the major source of their emissions. The Igeo index indicated moderate to extremely contaminated levels of Cu, Pb, Cd, and Ni in Karachi, Lahore and Gujranwala. Ingestion was found as a leading human exposure route, followed by dermal and inhalation exposure, with Pb posing the greatest health risk. The Cumulative Incremental Lifetime Cancer Risk (ILCR) model suggested moderate to low cancer risks for workers. Strategic interventions recommend mitigating health and environmental risks, prioritizing human health and ecosystem integrity in Pakistan's e-waste management.

Seasonal variability of airborne mold concentrations as related to dust in a coastal urban area in the Eastern Mediterranean.

Recent studies have demonstrated that the amount of specific airborne mold types and their concentrations increase during dust events. This study investigates the seasonal variation of airborne mold concentrations before, during, and after the dust transport in an eastern Mediterranean coastal area, Izmir city, Turkey. A total of 136 airborne mold samples were collected between September 2020 and May 2021. Two different culture media, namely Potato Dextrose Agar (PDA) and Malt-Extract Agar (MEA), were used for enumeration and genus-based identification of the airborne mold. In addition to culture media, the influences of air temperature, relative humidity, and particulate matter equal to or less than 10 µm (PM10) were also investigated seasonally. The HYSPLIT trajectory model and web-based simulation results were mainly used to determine dusty days. The mean total mold concentrations (TMC) on dusty days (543 Colony Forming Unit (CFU)/m3 on PDA and 668 CFU/m3 on MEA) were approximately 2-2.5 times higher than those on non-dusty days (288 CFU/m3 on PDA and 254 CFU/m3 on MEA) for both culture media. TMC levels showed seasonal variations (p < 0.001), indicating that meteorological parameters influenced mold concentrations and compositions. Some mold genera, including Cladosporium sp., Chrysosporium sp., Aspergillus sp., Bipolaris sp., Alternaria sp., and yeast, were found higher during dusty days than non-dusty days. Thus, dust event impacts levels and types of airborne molds and has implications for regions where long-range dust transport widely occurs.

Gaseous elemental mercury emissions from informal E-Waste recycling facilities in Pakistan.

Detrimental effects of mercury (Hg) on ecosystems and human health have been well-documented. Whereas emissions of gaseous elemental mercury (GEM) from e-waste recycling have been reported in developed countries, much less is known about the situation in the Global South. Using a total of 132 passive air samplers, seasonally resolved concentrations of GEM in air were measured continuously at 32 informal e-waste recycling facilities and background location in Pakistan for a period of one year between September 2020 and December 2021. Annual average GEM concentrations at the studied locations ranged from 1.8 to 92 ng m-3. Among the studied cities, higher concentrations were measured in Karachi (mean ± s.d: 17 ± 22, range: 4.2-92 ng m-3), Lahore (16 ± 4.2, 8.2-22 ng m-3) and Peshawar (15 ± 17, 4.9-80 ng m-3), while lower levels were measured in Hyderabad (6.9 ± 6.2, 3.1-25 ng m-3), consistent with a higher rate of informal recycling activities in metropolitan areas. Seasonally, higher GEM levels occurred during autumn (15 ± 16: 3.3-92 ng m-3) and summer (13 ± 8.7: 1.8-80 ng m-3) than in winter (12 ± 8.4: 2.5-49 ng m-3) and spring (9.2 ± 7.3: 1.8-80 ng m-3), possibly reflecting enhanced volatilization at higher temperatures and/or varying magnitude of recycling operations in different seasons. Policies and strict regulations related to e-waste management should be developed and implemented urgently in the country.

Existence of SARS-CoV-2 RNA on ambient particulate matter samples: A nationwide study in Turkey.

Coronavirus disease 2019 (COVID-19) is caused by the SARS-CoV-2 virus and has been affecting the world since the end of 2019. The disease led to significant mortality and morbidity in Turkey, since the first case was reported on March 11th, 2020. Studies suggest a positive association between air pollution and SARS-CoV-2 infection. The aim of the present study was to investigate the role of ambient particulate matters (PM), as potential carriers for SARS-CoV-2. Ambient PM samples in various size ranges were collected from 13 sites including urban and urban-background locations and hospital gardens in 10 cities across Turkey between 13th of May and 14th of June 2020 to investigate the possible presence of SARS-CoV-2 RNA on ambient PM. A total of 203 daily samples (TSP, n = 80; PM2.5, n = 33; PM2.5-10, n = 23; PM10µm, n = 19; and 6 size segregated PM, n = 48) were collected using various samplers. The N1 gene and RdRP gene expressions were analyzed for the presence of SARS-CoV-2, as suggested by the Centers for Disease Control and Prevention (CDC). According to real time (RT)-PCR and three-dimensional (3D) digital (d) PCR analysis, dual RdRP and N1 gene positivity were detected in 20 (9.8%) samples. Ambient PM-bound SARS-CoV-2 was analyzed quantitatively and the air concentrations of the virus ranged from 0.1 copies/m3 to 23 copies/m3. The highest percentages of virus detection on PM samples were from hospital gardens in Tekirdag, Zonguldak, and Istanbul, especially in PM2.5 mode. Findings of this study have suggested that SARS-CoV-2 may be transported by ambient particles, especially at sites close to the infection hot-spots. However, whether this has an impact on the spread of the virus infection remains to be determined.

Determination of real-world emission factors of trace metals, EC, OC, BTEX, and semivolatile organic compounds (PAHs, PCBs and PCNs) in a rural tunnel in Bilecik, Turkey.

A field study was performed in a rural tunnel to determine pollutant concentrations, sources and on road vehicle emission factors (EFs) of particulate matter, trace metals, elemental carbon (EC), organic carbon (OC), benzene, toluene, ethyl benzene and xylenes (BTEX), and polycyclic aromatic hydrocarbons (PAHs). Emission factors (EFs) for polychlorinated naphthalenes (PCNs) and polychlorinated biphenyls (PCBs) were also determined. A 12-day extensive sampling campaign during morning and afternoon periods at inlet and exit stations of the tunnel was conducted. Morphology of the particles was also investigated by Scanning Electron Microcopy (SEM). Correlation analysis, factor analysis and diagnostic PAH ratios were utilized to identify emission sources of trace metals. Identified sources include brake wear (33%), resuspension of road dust (15%), tyre wear (12%), exhaust emissions (10%), and lubricants (9%). Based on the PAH diagnostic ratios, major sources of PAHs were estimated as diesel emissions. EFs were comparable with the literature and varied from 31.5 to 295.4 mg vehicle-1 km-1 with an average of 129.2 ±â€¯80 mg vehicle-1 km-1 for PM2.5. PM2.5-10 EFs varied between 15.9 and 236.1 mg vehicle-1 km-1 with an average of 96 ±â€¯30 mg vehicle-1 km-1. Average EC EFs were 40.3 ±â€¯9.8 mg vehicle-1 km-1 for PM2.5 samples and 19.5 ±â€¯0.5 mg vehicle-1 km-1 for PM2.5-10 samples while OC EFs were 33.7 ±â€¯18 and 15.5 ±â€¯8.4 mg vehicle-1 km-1 for fine and coarse particles, respectively. EFs of elements were generally 2 (Al) to 59 (Mg) times higher than those previously reported in the literature. Compared to literature, relatively higher EFs for Σ13PAHs (range: 48.1-168 µg vehicle-1 km-1, average: 84.3 ±â€¯46.4 µg vehicle-1 km-1) were obtained. BTEX emission factors were in the range of 4.2 ±â€¯4.7 mg vehicle-1 km-1 (m + p-xylene) and 16.7 ±â€¯10.5 mg vehicle-1 km-1 (toluene). Average EFs for ΣPCBs and ΣPCNs were 12.06 ±â€¯5.3 µg vehicle-1 km-1 and 88.9 ±â€¯70.4 ng vehicle-1 km-1, respectively.

Spatial variation of PAHs and PCBs in coastal air, seawater, and sediments in a heavily industrialized region.

Concurrent coastal seawater (n = 22), sediment (n = 22), and atmospheric samples (n = 10) were collected in the Aliaga industrial region, Turkey, to explore the spatial variation, sources, and air-seawater exchange of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Seawater Σ16PAH concentrations (particle + dissolved) ranged between 5107 and 294,624 pg L-1, while Σ41PCB concentrations were in the range of 880-50,829 pg L-1. Levels in sediments were highly variable ranging between 35.5-49,682 and 2.7-2450 µg kg-1 in dry weight for Σ16PAHs and Σ41PCBs, respectively. Atmospheric concentrations varied between 1791-274,974 and 104-20,083 pg m-3 for Σ16PAHs and Σ41PCBs, respectively. Sediment organic matter (OM) content and levels of Σ16PAHs and Σ41PCBs correlated weakly (r 2 = 0.19-0.23, p < 0.05) suggesting that the spatial variations of PAHs and PCBs were mainly affected by local sources rather than their sorption to OM. The geographical distribution of PAH and PCB concentrations in air, seawater, and sediment and factor analysis on the sediment levels pointed out that the major sources in the region are steel plants, petroleum refinery, petrochemical complex, ship breaking, loading/unloading activities at the ports, vehicular emissions, and fossil fuel combustion emissions. The direction of the air-seawater exchange was also explored by estimating seawater fugacity fractions of PAHs and PCBs. For PAHs, the number of cases implying deposition (43.0%) and volatilization (39.5%) was similar, while for PCBs, the number of cases implying volatilization (60.4%) was much higher compared to deposition (21.6%). Fugacity fractions were generally <0.36 (deposition) at the sites close to industrial and ship breaking activities where the highest seawater and sediment levels were measured, implying that atmospheric deposition is an important mechanism affecting seawater and sediment PAH and PCB levels.

Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces.

Polychlorinated naphthalene (PCN) emissions of scrap iron processing steel plants were explored by measuring concentrations in stack gases of five plants, in the atmosphere (n=11) at a site close to those plants, and in soil at several sites in the region (n=40) in Aliaga, Izmir, Turkey. Observed stack-gas Σ32PCN levels from the plants without scrap preheating (189±157ngNm-3, average±SD, n=4) showed that they are substantial PCN emitting sources. Stack-gas Σ32PCN level for the plant with scrap preheating was considerably higher (1262ngNm-3). Similarly, Σ32PCN emission factor for this plant was substantially higher (11.9mgton-1) compared to those without scrap preheating (1.30±0.98mgton-1). Results have also suggested that the investigated steel plants emit large quantities of fugitive particle-phase PCNs. Measured soil Σ32PCN concentrations that are considered to be representative of the atmospheric levels were greatly variable in the region, ranging between 0.003 and 10.02µgkg-1 (dry wt). Their spatial distribution showed that main PCN sources in the region were the iron-steel plants. Ambient air levels (1620±800pgm-3) were substantially higher than ones observed around the world and in the study area verifying that the steel plants with electric arc furnaces (EAFs) are important PCN sources. Investigation of possible mechanisms suggested that the combustion processes also contribute to emissions from EAFs in addition to evaporation of PCNs present in the scrap iron.

Investigation of spatial and historical variations of air pollution around an industrial region using trace and macro elements in tree components.

Several trace and macro elements (n=48) were measured in pine needle, branch, bark, tree ring, litter, and soil samples collected at 27 sites (21 industrial, 6 background) to investigate their spatial and historical variation in Aliaga industrial region in Turkey. Concentrations generally decreased with distance from the sources and the lowest ones were measured at background sites far from major sources. Spatial distribution of anthropogenic trace elements indicated that their major sources in the region are the iron-steel plants, ship-breaking activities and the petroleum refinery. Patterns of 40 elements that were detected in most of the samples were also evaluated to assess their suitability for investigation of historical variations. Observed increasing trends of several trace and macro elements (As, Cr, Fe, Mo, Ni, V, Cu, Pb, Sb, Sn, and Hg) in the tree-ring samples were representative for the variations in anthropogenic emissions and resulting atmospheric concentrations in Aliaga region. It was shown that lanthanides (La, Ce, Pr, Nd, Sm, Gd, Dy, Er, Yb) could also be used for the investigation of historical variations due to specific industrial emissions (i.e., petroleum refining). Results of the present study showed that tree components, litter, and soil could be used to determine the spatial variations of atmospheric pollution in a region while tree rings could be used to assess the historical variations.

Investigation of spatial distributions and sources of persistent organic pollutants (POPs) in a heavily polluted industrial region using tree components.

Spatial distributions of persistent organic pollutants (POPs) were investigated in Iskenderun industrial region in Turkey. POP concentrations were measured in different tree components (i.e., pine needle, branch, bark, and stem) collected at several industrial and background sites (n = 27). Also, air, litter, and soil samples were analyzed to determine the relationship of atmospheric pollutants with tree components, litter, and soil. Spatial variation of measured concentrations and factor analysis showed that the iron-steel plants are the most important POP sources in Iskenderun area. Correlations of ambient air levels to those measured in soil, litter, and tree components were significant showing that POPs are exchanged between atmosphere and these compartments. Results have suggested that tree components, litter and soil could be used to determine the spatial distributions and sources of atmospheric POPs in a region. POP quantities (mg/ha) accumulated in different tree components, litter, and soil were also predicted. Generally, the highest quantities were accumulated by stem and needles. In terms of overall inventory, including trees, litter and soil, the highest accumulated quantities were found in soil followed by trees and litter, indicating that in addition to soil, vegetation is a notable reservoir accumulating POPs. Ambient air POP concentrations were also estimated using a bark/air partitioning model. The estimated/measured ratios were close to 1.0 for several compounds and the results showed that the atmospheric POP concentrations could be estimated from the bark measurements within factors of 0.23-3.07, 1.02-6.67, 0.63-7.44, 1.07-3.37 for polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polychlorinated naphthalenes, and polybrominated diphenyl ethers, respectively.

Biogenic volatile organic compound (BVOC) emissions from forested areas in Turkey: determination of specific emission rates for thirty-one tree species.

Normalized biogenic volatile organic compound (BVOC) emission rates for thirty one tree species that cover the 98% of national forested areas in Turkey were determined. Field samplings were performed at fourteen different forested areas in Turkey using a specific dynamic enclosure system. The selected branches of tree species were enclosed in a chamber consisted of a transparent Nalofan bag. The air-flows were sampled from both inlet and outlet of the chamber by Tenax-filled sorbent tubes during photosynthesis of trees under the presence of sunlight. Several environmental parameters (temperature, humidity, photosynthetically active radiation-PAR, and CO2) were continuously monitored inside and outside the enclosure chamber during the samplings. Collected samples were analyzed using a gas chromatography mass spectrometry (GC/MS) system equipped with a thermal desorber (TD). Sixty five BVOCs classified in five major groups (isoprene, monoterpenes, sesquiterpenes, oxygenated sesquiterpenes, and other oxygenated compounds) were analyzed. Emission rates were determined by normalization to standard conditions (1000 µmol/m(2)s PAR and 30 °C temperature for isoprene and 30 °C temperature for the remaining compounds). In agreement with the literature, isoprene was mostly emitted by broad-leaved trees while coniferous species mainly emitted monoterpenes. Several tree species such as Sweet Chestnut, Silver Lime, and European Alder had higher monoterpene emissions although they are broad-leaved species. High isoprene emissions were also observed for a few coniferous species such as Nordmann Fir and Oriental Spruce. The highest normalized total BVOC emission rate of 27.1 µg/gh was observed for Oriental Plane while South European Flowering Ash was the weakest BVOC emitter with a total normalized emission rate of 0.031 µg/gh. Monoterpene emissions of broad-leaved species mainly consisted of sabinene, limonene and trans-beta-ocimene, while alpha-pinene, beta-pinene and beta-myrcene were generally emitted by coniferous species. Oxygenated compounds were the third most prominent BVOC group and sesquiterpenes had slightly lower contributions.