Metal characterization of airborne particulate matters in a coastal region

The concentrations of suspended particulate matter in the air of the Orissa Sand Complex had an average value of 128 ± 10 µg m^?3 in residential areas and 170 ± 8 µg m^?3 in mining areas. PM₁₀ levels in residential areas were found to have an average of 35 ± 10 µg m^?3, in mining areas 45 ± 10 µg m^?3. The distribution of some elements is also discussed here. Inhalation doses were observed to be higher in summer than in winter and the rainy season. The highest dose rate was for the age group of 1 year, and health risks were found to be highest for the same. For adults, inhalation dose and health risk are 1.3 times higher in mining than in residential areas.     

Dependency of polycyclic aromatic hydrocarbon concentrations on particle size distribution in Tehran atmosphere

In this work, the airborne particulate matter with an aerodynamic diameter less than 10 µm (PM₁₀) was fractionated in a six-stage high-volume cascade impactor to identify particulate size distribution in Tehran atmosphere. The study was conducted at 15 sites located in the north, south, east, west, and central parts of Tehran in 2005. Air samples were analyzed for 16 polycyclic aromatic hydrocarbons (PAHs) by HPLC. The daily PM₁₀ concentrations at the peak of traffic in roadside areas were found to be 106–560 µg m^?3. The cumulated concentration sum of PAHs, based on 16 species, was found to have an average concentration of 380 ng m^?3. Furthermore, it was found that more than 60% of PAHs belonged to the small particulate size range, having sizes of less than 0.49 µm, some containing benzo(ghi)perylene and indeno(123cd)pyrene (high molecular weight) with average concentrations of 8 and 6 ng m^?3 and fluorene, phenanthrene, and fluoranthene (low molecular weight) with average concentrations of 14, 13, and 19 ng m^?3, respectively. In addition, the results revealed that the lighter three- and four-ring PAH compounds were the most abundant pollutants in the air collected at all the sampling sites.     

Temporal variability in atmospheric Hg released from natural and anthropogenic sources in central Taiwan

From September 2011 to February 2012, ambient air particulate and particulate-bound mercury [Hg(p)] concentrations were measured, together with dry deposition using a cold vapor atomic fluorescence spectrometry (CVAFS) analyser, at two characteristic sampling sites in central Taiwan. Results from the sampling site at Westin Park indicated that the lowest particulate dry deposition and lowest average particulate concentrations in total suspended particles (TSP) occurred in September (29.70±7.47 μ g m^?2×min) and February (34.38±13.60 ng m^?3), respectively. Moreover, results from the Gung-Ming junior high school (airport) site, showed that the highest average particulate dry deposition and average highest particulate concentrations in TSP occurred in February (156.76±30.36 μ g m^?2×min) and January (125.49±9.51 ng m^?3), respectively, during the winter. The Dragon Steel Plant and Han-Shian Aerospace Industrial Development Corporation were both nearby. These factors led to the high Hg(p) concentrations at Taichung Airport (TA) compared with Westin Park. Local large suspended particulates from heavy traffic were the main reason for the high average Hg(p) deposition at Westin Park compared with TA in this study.     

Source identification of particulate matter and associated intake of elements through inhalation in an industrial area of Odisha,India

Particulate matter concentrations were measured in an industrial region in the Ganjam district of Odisha. The average levels of suspended particulate matter (SPM) were measured to be 142 ± 8 and PM₁₀ of particulate matter with a size of less than 10 micrometers (PM₁₀) to be 50 ± 15 μg m^?3. Out of the 14 elements determined, Ca, Na, Mg, Fe, and K contributed more than 95% of the total weight. In enrichment factors, the trace elements, i.e., Zn, Pb, Cd, and Hg were observed to be highly enriched in the SPM and PM₁₀. Factor analysis indicates that more than 75% of the variance was due to five component factors, which have eigenvalues greater than 1. Intake of elements through inhalation route to adults has been estimated.     

Airborne fine particulate matter (PM2.5) at industrial,high- and low-density residential sites in a Nigerian megacity

Abstract

Airborne particulate matter PM_2.5 was collected in an industrial, a low-density, and a high-density residential area of Lagos from December 2010 to November 2011, and elemental composition was determined by proton-induced X-ray emission. Across the months, mass concentrations ranged from 13 to 237?µg?m^?3, exceeding the World Health Organization guideline value of 10?µg?m^?3. Data on 24 elements were obtained, with maximum values during Harmattan season months; source identification and apportionment studies by positive matrix factorization suggested that petroleum oil combustion (70%) was the major source of PM_2.5 and could pose a great hazard to Lagos receptors.     

Distribution,geochemistry, and mineralogy of aerosols in the Angouran Mine area,northwest Iran

The Angouran Mine, located in northwest Iran, is the largest Zn–Pb producer in the Middle East. This study was designed to investigate the distribution, geochemistry, and mineralogy of the aerosols in the mining area and to assess their likely health impacts on the local residents. For this purpose, 36 aerosol samples were collected from 2014 to 2015 at nine sites located in mine district and upwind and downwind directions. The concentration of potentially toxic elements in the aerosols was determined using AAS instrument. Size, morphology, and mineralogy of the particles were studied using SEM and EDX spectra. The results indicate that the amount of total suspended particles in upwind, mine district, and downwind sites is 95.5, 463.4 and 287.5 µg/m³, respectively. The concentrations of PM_2.5 in the three locations are 8.9, 134.7, and 51.8 µg/m³, whereas the PM₁₀ contents are 2.9, 74.4, and 15.5 µg/m³, respectively. These observations point to the impact of mining activities on the concentration of aerosols in the local atmosphere. The values of air quality index also show the probable effects of the mining activities on the health of the local populations, especially for allergic peoples. The average concentration of Zn in the samples collected from the mining district (290 µg/kg) is much higher than its value in the upwind sites (27 µg/kg). The highest concentration of As (70 µg/kg), Cd (10 µg/kg), and Pb (3 µg/kg) is in downwind sites, which shows the negative impact of mining activities on the local air quality. Temporally, the highest concentration of the studied elements is recorded in spring season, especially for PM_2.5 collected in downwind stations. Based on the results of SEM and EDX spectra, three groups of minerals, i.e., carbonates, silicates, and sulfides, are present in the aerosol particles, confirming the local source for the aerosols. SEM analyses showed that the aerosol particles with dissimilar chemical composition have different morphologies such as irregular, rounded, elongated, and angular. On the basis of the results, the mining activities in the Angouran Zn–Pb Mine may have various short- and long-term consequences on the public health, especially due to high amount of the finer particles (PM_2.5) and the higher concentration of the potentially toxic elements in PM_2.5 which can penetrate into the lungs.

     

Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System

Abstract

The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l^?1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l^?1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l^?1; the particulate organic carbon concentration was 212 ± 106 μg l^?1 and the isotopic composition was 18.77 ± 2.51%_°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ¹³C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.

Spatial differences in δ¹³C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In     

Speciation of mercury in South African coals

Total mercury (Hg_TOT) concentrations were determined by inductively coupled plasma mass spectrometry (ICP MS) for South African Highveld coals. The distribution of Hg in coals was investigated using a four-stage sequential leaching protocol and isotope dilution/gas chromatography coupled to ICP MS (ID-GC-ICP MS). The results show that Hg_TOT ranged from 144 to 303?µg?kg^?1 with a mean of 199?±?26?µg?kg^?1, while Hg_TOT leached from coals using different solvents ranged between 103 and 310?µg?kg^?1 (mean: 218?±?60?µg?kg^?1). Hg leaching rates of 53–78% were achieved in crushed coals. Hg⁰, Hg²⁺, and CH₃Hg⁺ were identified in all coals. CH₃Hg⁺ in studied coals ranged between 0.1 and 0.4 (mean: 0.2) µg?kg^?1. GC ICP MS chromatograms also showed unknown Hg peaks which were identified as other organomercury species such as ethylmercury. Modes of occurrence of Hg in coals were variable with the organic-bound (37–40%) and the sulfide-bound (37–39%) being the dominant mercury forms. Increasing the HCl concentration in the used protocol increased the amount of Hg leached (16%) during this step.     

Concentrations of lead in cosmetics commonly used in South Africa

In this study, we present evidence of lead in lip liner, oil absorbent powder, mascara, concealer, lipsticks, lip gloss, and foundation. The samples were analyzed for lead by flame atomic absorption spectrometry. The levels of lead in concealer, mascara, lip liner, and oil absorbent powder were found to be 7.4?±?1.3?µg?g^?1, 15.8?±?0.2?µg?g^?1, 29.0?±?9.2?µg?g^?1, and 17.3?±?2.9?µg?g^?1, respectively. The levels of lead in lipsticks, lip gloss, and foundation ranged from not detected to 73.1?±?5.2?µg?g^?1, 4.7 to 11.7?±?2.8?µg?g^?1, and 7.8 to 32.9?±?1.4?µg?g^?1, respectively. Thus, in the majority of samples, the concentrations of lead are higher than the USFDA maximum permissible concentration of 0.10?µg?g^?1 in candy and cosmetics. In lipsticks alone, only 25% of 40 samples were found to meet the requirement. Therefore, continuous use of cosmetic products in which lead concentration exceeds the maximum permissible level may pose a health hazard for the female population of South Africa in the long run.     

Trace element concentration in fine particulate matter (PM<Subscript>2.5</Subscript>) and their bioavailability in different microenvironments in Agra,India: a case study

Exposure to airborne particulate matter results in the deposition of millions of particle in the lung; consequently, there is need for monitoring them particularly in indoor environments. Case study was conducted in three different microenvironments, i.e., urban, rural and roadside to examine the elemental bioavailability in fine particulate matter and its potential health risk. The samples were collected on polytetrafluoroethylene filter paper with the help of fine particulate sampler during August–September, 2012. The average mass concentration of PM_2.5 was 71.23 µg m^?3 (rural), 45.33 µg m^?3 (urban) and 36.71 µg m^?3 (roadside). Elements in PM_2.5 were analyzed by inductively coupled plasma atomic emission spectroscopy. Percentage bioavailability was determined to know the amount of soluble fraction that is actually taken across the cell membrane through inhalation pathway. Cadmium and lead were found to have cancer risk in a risk evaluation using an Integrated Risk Information system.     

Characteristics,sources and health risk assessment of toxic heavy metals in PM<Subscript>2.5</Subscript> at a megacity of southwest China

Twenty trace elements in fine particulate matters (i.e., PM_2.5) at urban Chengdu, a southwest megacity of China, were determined to study the characteristics, sources and human health risk of particulate toxic heavy metals. This work mainly focused on eight toxic heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The average concentration of PM_2.5 was 165.1 ± 84.7 µg m^?3 during the study period, significantly exceeding the National Ambient Air Quality Standard (35 µg m^?3 in annual average). The particulate heavy metal pollution was very serious in which Cd and As concentrations in PM_2.5 significantly surpassed the WHO standard. The enrichment factor values of heavy metals were typically higher than 10, suggesting that they were mainly influenced by anthropogenic sources. More specifically, the Cr, Mn and Ni were slightly enriched, Cu was highly enriched, while As, Cd, Pb and Zn were severely enriched. The results of correlation analysis showed that Cd may come from metallurgy and mechanical manufacturing emissions, and the other metals were predominately influenced by traffic emissions and coal combustion. The results of health risk assessment indicated that As, Mn and Cd would pose a significant non-carcinogenic health risk to both children and adults, while Cr would cause carcinogenic risk. Other toxic heavy metals were within a safe level.     

Distribution of polychlorinated biphenyls and polybrominated diphenyl ethers in soils of a previous E-waste processing center

Surface soil samples were taken from a previous electronic waste (E-waste) recycling centerin Taizhou area, Zhejiang province, China. Concentrations, profiles, and possible sources of 19 polychlorinated biphenyls and 7 poly-brominated diphenyl ethers were analyzed to assess their current state in the soil after phase out of massive dismantling of E-wastes. The concentrations of the 7 polybrominated diphenyl ethers ranged from 11 to 128 µg kg^?1 with an average of 41 ± 10 µg kg^?1 (dw), with 2,2′,4,4′-tetrabromdiphenyl ether being the most abundant. These values were substantially lower than the levels in 2006. The concentrations of the 19 polychlorinated biphenyls ranged from 36 to 760 µg kg^?1, with an average of 181 ± 68 µgkg^?1 (dw) which was also lower than the levels in 1995 or 2006. However, the concentrations of some tetra-, penta- and hexa-chlorobiphenyls were comparable or even higher than before. Furthermore, the average concentration of 7 indicator polychlorinated biphenyls was 108 ± 41 µg kg^?1(dw) which exceeded the New Dutch List target value of 20 µgkg^?1. Principal component analysis indicated that polychlorinated biphenyls were mainly distributed into three groups in accordance with the number of chlorine atoms and anthropogenic source. Therefore, the impact of the historical dismantling of E-wastes is still significant.     

Pollution characteristics of particulate matters emitted from outdoor barbecue cooking in urban Jinan in eastern China

To understand the pollution characteristics of particulate matter emitted from outdoor barbecue cooking in eastern China, measurements of the PM_2.5 mass concentration, the number concentration of particles with a diameter of 0.01 to 1.0 μm, and the particle size distribution from 0.3 to 25 μm were carried out at seven barbecue restaurants in urban Jinan. The average PM_2.5 mass concentration and sub-micron particle number concentrations at a distance of 1 m from the grills were 250 to 1083 μg/m³ and 0.90 × 10⁵ to 2.23 × 10⁵ cm^–3, respectively, which were much higher than those in the ambient air of the urban area. Compared to the ambient atmosphere, barbecue cooking emitted very high levels of particles with a larger increase in the concentrations of super-micron particles than that of sub-micron particles. The super-micron particle number concentrations at the barbecue restaurants were 10 to 100 times higher than those observed in the ambient urban atmosphere. The barbecue smoke had a significant effect on the particle concentrations in the surrounding region. Both mass and number concentrations of particles exhibited maximum values immediately near the barbecue grills and often reached a peak at a distance of 10 to 15 m. The removal efficiency of a range hood for the cooking particles was tested in an indoor kitchen. The range hood effectively cleaned the particulate matter pollution caused by cooking with a removal efficiency larger than 80%. Therefore, the use of a range hood is recommended for outdoor barbecue restaurants coupled with a smoke purifier to clean the emitted high concentrations of particles.

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Arsenic in freshwater ecosystems of the Bengal delta: status,sources and seasonal variability

The study aimed to examine the contamination status of arsenic (As) in excavated small water bodies, commonly known as ponds – the integral part of daily life in the arsenic-affected rural areas of West Bengal, India in comparison to the unaffected areas. The ponds of the contaminated area had higher levels of As: water 2–174 µg L^?1 (mean 31 ± 2 µg L^?1) and sediment 1.3–37.3 mg kg^?1 (mean 10.3 ± 0.4 mg kg^?1), than those from the unaffected area: water 1–8 µg L^?1 (mean 4 ± 0 µg L^?1) and sediment 1.4–5.3 mg kg^?1 (mean 3.0 ± 0.1 mg kg^?1). A moderate positive correlation was observed between the water and sediment arsenic content of the ponds of the arsenic-affected region (r = 0.688, n = 277, p < 0.0001). Contaminated ground water, either as direct input or through agricultural washings, was found to be the major contributor of arsenic pollution to these ecosystems. Seasonal variations were not prominent. This study emphasized the beneficial role of using the studied ecosystems over the highly contaminated ground water for various livelihood activities in the Gangetic delta region.     

Oxidative potential (OP) and mineralogy of iron ore particulate matter at the Gol-E-Gohar Mining and Industrial Facility (Iran)

Concentrations of total suspended particulate matter, particulate matter with aerodynamic diameter <2.5 μm (PM_2.5), particulate matter <10 μm (PM₁₀), and fallout dust were measured at the Iranian Gol-E-Gohar Mining and Industrial Facility. Samples were characterized in terms of mineralogy, morphology, and oxidative potential. Results show that indoor samples exceeded the 24-h PM_2.5 and PM₁₀ mass concentration limits (35 and 150 µg m^?3, respectively) set by the US National Ambient Air Quality Standards. Calcite, magnetite, tremolite, pyrite, talc, and clay minerals such as kaolinite, vermiculite, and illite are the major phases of the iron ore PM. Accessory minerals are quartz, dolomite, hematite, actinolite, biotite, albite, nimite, laumontite, diopside, and muscovite. The scanning electron microscope structure of fibrous-elongated minerals revealed individual fibers in the range of 1.5 nm to 71.65 µm in length and 0.2 nm to 3.7 µm in diameter. The presence of minerals related to respiratory diseases, such as talc, crystalline silica, and needle-shaped minerals like amphibole asbestos (tremolite and actinolite), strongly suggests the need for detailed health-based studies in the region. The particulate samples show low to medium oxidative potential per unit of mass, in relation to an urban road side control, being more reactive with ascorbate than with glutathione or urate. However, the PM oxidative potential per volume of air is exceptionally high, confirming that the workers are exposed to a considerable oxidative environment. PM released by iron ore mining and processing activities should be considered a potential health risk to the mine workers and nearby employees, and strategies to combat the issue are suggested.     

Platinum in PM2.5 of the metropolitan area of Mexico City

The increase in platinum (Pt) in the airborne particulate matter with size ≤2.5 µm (PM_2.5) in urban environments may be interpreted as result of the abrasion and deterioration of automobile catalyst. Nowadays, about four million vehicles in Mexico City use catalytic converters, which means that their impact should be considered. In order to evaluate the contribution of Pt to environmental pollution of the metropolitan area of Mexico City (MAMC), airborne PM_2.5 was collected at five different sites in the urban area (NW, NE, C, SW, SE) in 2011 during April (dry-warm season), August (rainy season) and December (dry-cold season). Analytical determinations were carried out using a ICP-MS with a collision cell and kinetic energy discrimination. The analytical and instrument performance was evaluated with standard road dust reference material (BCR-723). Median Pt concentration in the analyzed particulate was is 38.4 pg m^?3 (minimal value 1 pg m^?3 maximal value 79 pg m^?3). Obtained Pt concentrations are higher than those reported for other urban areas. Spatial variation shows that SW had Pt concentration significantly higher than NW and C only. Seasonal variation shows that Pt median was higher in rainy season than in both dry seasons. A comparison of these results with previously reported data of PM₁₀ from 1991 and 2003 in the same studied area shows a worrying increase in the concentration of Pt in the air environment of MAMC.     

Spatial and Temporal Changes of Suspended Matter in Relation to Wind and Vegetation Cover in A Mediterranean Shallow Coastal Environment

Abstract

Seasonal and spatial changes in seston, (POC), particulate organic carbon, (PON) particulate organic nitrogen and chlorophyll-a concentrations were studied on a monthly basis in a Mediterranean shallow coastal area (Stagnone di Marsala, Western Sicily) in order to gather information on factors controlling particulate organic matter distribution and composition. Seston concentration and composition were connected to the main physicochemical and biological driving factors, such as temperature, salinity, dissolved oxygen, wind-speed and biomass of submerged vegetation. the Stagnone di Marsala is characterized by high temperatures with strong seasonality (range: 11–28°C), while values ranged from 33 to 45 salinity. Total suspended organic matter concentrations (by ignition loss) ranged from 2 mg l^?1 (in summer) to 12mgl^?1 (in winter) and chlorophyll-a concentrations from 0.02 to 2 μgl^?1. Despite a low POC/PON ratios (ranging from 5 to 11), the ratio of POC to chlorophyll (CHL-a) displayed very high values (annual average of 647). the data reported in this study, highlighting the oligotrophy of the Stagnone di Marsala area, indicate that the trophic state of the basin was controlled by different degrees of wind exposure (mean monthly wind velocity at exposed sites ranged between 4.2 and 6.7 m s^?1) and by gradients in vegetation cover. These two factors induced clear changes in the concentration and composition of the suspended particles, but played a different role in exposed and sheltered areas. Exposed areas with limited vegetation were characterized by large resuspension processes and wide temperature and salinity fluctuations caused by wind induced turbulence. in these areas, autotrophic biomass (as chlorophyll-a), due to phytoplankton and/or re-suspended microphytobenthos, appeared to play an important     

Genotoxic and cytotoxic in vitro evaluation of ivermectin and its formulation ivomec® on Aedes albopictus larvae (CCL-126™) cells

Genotoxic effects of ivermectin (IVM) and its commercial formulation ivomec® (IVM 1.0%) were studied on Aedes albopictus larvae (CCL-126?) cells by sister chromatid exchange (SCE) and single cell gel electrophoresis (SCGE) while cytotoxicity was determined by cell-cycle progression (CCP), proliferative rate index (PRI), mitotic index (MI), 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), and neutral red (NR) endpoints within a 1–250 µg mL^?1 concentration range. While IVM and ivomec® did not markedly affect SCE frequencies, these agents induced DNA-strand breaks enhancing both slightly damaged and damaged cells at 25–50 and 5–50 µg mL^?1 IVM and ivomec®, respectively. Both compounds exerted a delay in CCP and reduction of PRI at 10 µg mL^?1. Cytotoxicity was observed at concentrations higher than 25 µg mL^?1. A marked reduction of about 98% and 94% of MI compared to controls was noted with 25 µg mL^?1 of IVM and ivomec®, respectively. NR and MTT assays revealed that both compounds induced a cell growth inhibition within the 1–250 µg mL^?1 concentration range. Data indicated that IVM and ivomec® exert both genotoxicity and cytotoxicity in insect cells in vitro, at least in A. albopictus larvae CCL-126? cells.     

Uranium quantification in groundwater and health risk from its ingestion in Haryana,India

Uranium is a naturally occurring radioactive element which may cause toxicological or radiological hazards to the public if present in drinking water. This study reports the quantification of uranium in groundwater of major towns of the district Fatehabad, Haryana, India. Uranium concentrations ranged between 0.3 and 48 μg L^?1. In 22% of the groundwater samples, uranium concentrations were higher than the World Health Organization maximum permissible limit of 30 µg L^?1. The radiological dose for males was found to be in the range of 4.8?×?10^?4–7.1?×?10^?2 mSv y^?1 and for females 3.5?×?10^?4–5.2?×?10^?2 mSv y^?1. The results showed that due to the ingestion of groundwater in the study area, radiological cancer risk is in the range of 9.1?×?10^?7–1.3?×?10^?4, lower than the risk limit. Uranium ingestion from groundwater varied from 0.02 to 3.5 µg kg^?1 day^?1, which is within acceptable limit.     

Sediment-associated trace and major metals in the headwaters of a tropical reservoir

Bed sediment samples of the two headwaters of a tropical reservoir in Southwestern Nigeria were analysed for some metal concentrations using ICP-OES for a period of one year. Sediment samples were collected bi-monthly from both the lower and upper reaches of the streams from May 2013 to March 2014. Sediment samples were microwave-digested and analysed using ICP-OES. Concentrations of metals were higher in the lower reach than in the upper reach, and wet season concentrations were higher than in the dry season with the exception of Fe and Mn. The annual mean metal concentrations were as follows: Fe (121.72?±?6.82?µg/g); Mn (9.34?±?2.57?µg/g); Na (6.20?±?2.29?µg/g); K (0.65?±?0.57?µg/g); Mg (8.07?±?1.36?µg/g); Ca (13.92?±?2.85?µg/g); Ba (0.17?±?0.17?µg/g); Al (106.54?±?5.55?µg/g); and Se (0.6?±?0.19?µg/g). These values were lower in comparison with the baseline concentrations of elements on the earth’s crust. Contamination assessment of all the metals investigated in this study showed that metals in the bed sediments of the two headstreams had not reached pollution status with the exception of Se.