Pressure Changes Across a Membrane Formed by Coacervation of Oppositely Charged Polymer-Surfactant Systems.

We investigate the mass transfer and membrane growth processes during capsule formation by the interaction of the biopolymer xanthan gum with CnTAB surfactants. When a drop of xanthan gum polymer solution is added to the surfactant solution, a membrane is formed by coacervation. It encapsulates the polymer drop in the surfactant solution. The underlying mechanisms and dynamic processes during capsule formation are not yet understood in detail. Therefore, we characterized the polymer-surfactant complex formation during coacervation by measuring the surface tension and surface elasticity at the solution-air interface for different surfactant chain lengths and concentrations. The adsorption behavior of the mixed polymer-surfactant system at the solution-air interface supports the understanding of observed trends during the capsule formation. We further measured the change in capsule pressure over time and simultaneously imaged the membrane growth via confocal microscopy. The cross-linking and shrinkage during the membrane formation by coacervation leads to an increasing tensile stress in the elastic membrane, resulting in a rapid pressure rise. Afterward, the pressure gradually decreases and the capsule shrinks as water diffuses out. This is not only due to the initial capsule overpressure but also due to osmosis caused by the higher ionic strength of the surfactant solution outside the capsule compared to the polymer solution inside the capsule. The influence of polymer concentration and surfactant type and concentration on the pressure changes and the membrane structure are studied in this work, providing detailed insights into the dynamic membrane formation process by coacervation. This knowledge can be used to produce capsules with tailored membrane properties and to develop a suitable encapsulation protocol in technological applications. The obtained insights into the mass transfer of water across the capsule membrane are important for future usage in separation techniques and the food industry and allow us to better predict the capsule time stability.

Trophic transfer, bioaccumulation and translocation of microplastics in an international listed wetland on the Montreux record.

Microplastics (MPs) are concerning emerging pollutants. Here, MPs in four edible aquatic species of different trophic levels (between ∼2 and 4), including fish species Esox lucius (Esocidae: Esocinae); Cyprinus carpio (Cyprinidae: Cyprininae); and Luciobarbus caspius (Cyprinidae: Barbinae); and the swan mussel Anodonta cygnea (Unionidae), were assessed in the Anzali freshwater ecosystem. It is a listed wetland in the Montreux record. MPs were extracted from gastrointestinal tracts (GI), gills, muscles, and skin. All the studied fish and mussels (n = 33) had MPs. MP fibres, fragments and sheets were detected in every GI examined, however, fibres were the only type of MPs in skins, muscles and gills and were the most abundant MP. The MPs found in the fish and mussels were mainly made of nylon (35% of the total MPs), polypropylene-low density polyethylene (30%), and polycarbonate (25%). The average numbers of MPs found in every fish specimen, expressed per wet body mass, had a moderate negative correlation with the condition factor (K) (MP/g - K: Pearson correlation r = -0.413, p = 0.049), and there was no significant relation with the growth factor (b) (r = -0.376; p = 0.068). Importantly, Luciobarbus caspius (with trophic level 2.7-2.8) bioaccumulated MPs and presented a strong correlation between their MP contamination and age (r = 0.916 p < 0.05). Greater gill mass (or related factors) played an important role in the accumulation of MPs, and there was a strong correlation between these factors for Esox lucius and Cyprinus carpio (r = 0.876; r = 0.846; p < 0.05 respectively). The highest MP/g gills (1.91 ± 2.65) were in the filter feeder Anodonta cygnea inhabiting the benthic zone. Esox lucius (piscivorous, trophic level 4.1) was the most contaminated species overall (a total of 83 MPs in 8 individuals, with 0.92 MP/g fish), and their gills where MPs mainly accumulated. Cyprinus carpio was the most contaminated specimen (MPs in specimens), while the number of MPs per mass unit increased with the trophic level. Their feeding and ecological behavior in the aquatic habitat affected the level of accumulation. This work includes evidence of translocation of MPs within the aquatic organisms.

Foam fractionation Tags (F-Tags) enabling surfactant-free, activity-preserving recovery of enzymes.

Enzymes have become important tools in many industries. However, the full exploitation of their potential is currently limited by a lack of efficient and cost-effective methods for enzyme purification from microbial production. One technology that could solve this problem is foam fractionation. In this study, we show that diverse natural foam-stabilizing proteins fused as F-Tags to ß-lactamase, penicillin G acylase, and formate dehydrogenase, respectively, are able to mediate foaming and recovery of the enzymes by foam fractionation. The catalytic activity of all three candidates is largely preserved. Under appropriate fractionation conditions, especially when a wash buffer is used, some F-Tags also allow nearly complete separation of the target enzyme from a contaminating protein. We found that a larger distance between the F-Tag and the target enzyme has a positive effect on the maintenance of catalytic activity. However, we did not identify any particular sequence motifs or physical parameters that influenced performance as an F-tag. The best results were obtained with a short helical F-Tag, which was originally intended to serve only as a linker sequence. The findings of the study suggest that the development of molecular tags that enable the establishment of surfactant-free foam fractionation for enzyme workup is a promising method. KEY POINTS: • Foam-stabilizing proteins mediate activity-preserving foam fractionation of enzymes • Performance as an F-Tag is not restricted to particular structural motifs • Separation from untagged protein benefits from low foam stability and foam washings.

Urinary nitrate and sodium in a high-risk area for upper gastrointestinal cancers: Golestan Cohort Study☆.

BACKGROUND: The epidemiological evidence regarding the carcinogenicity of nitrate and sodium in drinking water is limited, partly because measuring the exposure at the individual level is complex. Most studies have used nitrate in water supplies as a proxy for individual exposure, but dietary intakes and other factors may contribute to the exposure. The present study investigates the factors associated with urinary nitrate and sodium in a high-risk area for esophageal and gastric cancers. METHODS: For this cross-sectional study, we used data and samples collected in 2004-2008 during the enrollment phase of the Golestan Cohort Study from a random sample of 349 participants (300 individuals from 24 rural villages and 49 from the city of Gonbad), stratified by average water nitrate in their district, the source of drinking water, and the usual dietary intake of nitrate and sodium. Nitrate, sodium, and creatinine were measured in a spot urine sample collected at the time of interview. We used the provincial cancer registry data to calculate the cumulative incidence rates of esophageal and gastric cancers for each location through June 1, 2020, and used weighted partial Pearson correlation to compare the incidence rates with median urinary nitrate and sodium in each village or the city. RESULTS: Among 349 participants (mean age±SD: 50.7 ± 8.6 years), about half (n = 170) used groundwater for drinking, and the use of groundwater was significantly more common in high-elevation locations (75.8%). The geometric mean of the creatinine-corrected urinary nitrate concentration was 68.3 mg/g cr (95%CI: 64.6,72.3), and the corresponding geometric mean for urinary sodium was 150.0 mmoL/g cr (95%CI: 139.6,161.1). After adjusting for confounders, urinary nitrate was associated with being a woman, drinking groundwater, and living in high-elevation locations, but not with estimated dietary intake. Urinary sodium concentration was significantly associated with monthly precipitation at the time of sampling but not with elevation or drinking water source. There were significant positive correlations between both median urinary nitrate and sodium in each location and esophageal cancer incidence rates adjusted for sex and age (r = 0.65 and r = 0.58, respectively, p < 0.01), but not with gastric cancer incidence. CONCLUSION: In a rural population at high risk for esophageal and gastric cancers, nitrate excretion was associated with living at a higher elevation and using groundwater for drinking. The associations between nitrate and sodium excretion with esophageal cancer incidence warrant future investigation.

Macronutrients, trace metals and health risk assessment in agricultural soil and edible plants of Mahshahr City, Iran.

In this study, we evaluate the geochemistry of macro- (Fe, P, Ca, S, K, Na, Mg) and micronutrients (Mo, Cu, Pb, Zn, Co, Mn, Cd, Sr, Cr, Hg, Se), along with possible health risks of heavy metals contamination in agricultural soils and vegetables of the Mahshahr industrial port in Iran. Calculation of geochemical coefficients revealed the low pollution load of Mahshahr agricultural soils. Most of the investigated elements exhibited lower concentrations in soil than international standards. Element concentrations in plant samples were far below the permissible values set by environmental agencies. Based on permissible values, there was deficiency of several soil elements, including Cu, in vegetables because they are mostly present in the soil residual phase. An exception was Mn, which is the most mobile element in soil. The transfer factor (TF) of elements showed the following trend: K > Na > P > S > Mo > Hg > Se > Zn > Cd > Cu > Mg > Mn > Ca > Cr > Co ≈ Fe = Pb. There was high transfer of major elements from soil to plants, and lower values for micronutrients and heavy metals. The calculated daily intake (DIM) and health risk index (HRI) for ten plant species for adults were < 1, while the HRI was larger than 1 for Mn via radish consumption. According to geochemical investigations and statistical tests such as principal component analysis, Kruskal-Wallis, and correlation coefficient calculations, plant species play the most important role in elemental uptake by plants.

Water quality stress to Amirkalayeh Wetland, Northern Iran.

Amirkalayeh Wetland, listed as wetlands of International Importance in the Ramsar Convention, exposes to severe water quality stress resulted from increase in dissolved ions and nutrients concentrations. In addition to in situ measurements of physicochemical parameters (electrical conductivity, pH, and temperature), a total number of 28 water samples were collected from Amirkalayeh Wetland and surrounding surface and groundwater resources to investigate the most important factors increasing trophic state and decreasing the water quality of the wetland. Water samples were analyzed for major ions and dissolved plant nutrients (nitrate, nitrite, ammonium, and phosphate). Up to three-time increase in salinity and dramatic rising in nutrients level was observed in Amirkalayeh Wetland from 2017 to 2021. The excessive nutrients intake resulted in hyper-eutrophication trophic status of Amirkalayeh Wetland. Our hydrological, hydrochemical, and statistical studies investigating the role of a variety of possible water quality degrading factors show that surface and subsurface drainage of agricultural return water into the Amirkalayeh Wetland are the major cause of increase in trophic level and decreasing water quality. Results of this work indicate that Amirkalayeh Wetland is exposed to severe water quality stress that threatens the aquatic life and ecosystem of this wetland. Therefore, preventing the inflow of surface and subsurface agricultural drains to the wetland and providing a sustainable water management plan are vital to improve water quality of the wetland.

Source and risk assessment of heavy metals and microplastics in bivalves and coastal sediments of the Northern Persian Gulf, Hormogzan Province.

The objectives of the current study are to investigate the concentration, biological risks, chemical speciation, and mobility of of heavy metals and also the determination of their distribution, physicochemical characteristics, and abundance of microplastics in coastal sediments and edible bivalves in the Persian Gulf, the coastal area of Hormozgan Province. Sampling points were selected considering the location of industrial, urban and Hara forest protected areas. In November 2017, a total of 18 sediment samples from coastal sediments (top 0-10 cm) and the most consumed bivalve species in the region were collected from two stations, Lengeh and Bandar Abbas Ports. The average concentration of heavy metals (except for Ni and Cd) in the sediments were lower than their average shale and the upper continental crust. Enrichment factors revealed significant enrichment of Ni, Mn, Cr, Cd and As. The fractionation of heavy metals using the Community Bureau of Reference (BCR) sequential extraction scheme indicated the high bioavailability of Zn, As, Mn, and Co. In general, the highest concentration of Mo, Cd, Pb, Zn, Cr, Cu, Mn, Hg, and Sb was detected in areas with frequent human activities including Shahid Rajaee Port, Shahid Bahonar Port, and Tavanir station. Shahid Rajaee and Shahid Bahonar Ports are the most important ports on the coast of Hormozgan province. The Risk Assessment Code calculated for the study elements indicates that As, Co, Zn, and Cu pose a moderate environmental risk a threat to the aquatic biota. Health risks of most heavy metals arising from bivalves consumption were safe, except for As which is associated with the high target cancer risk values. With reference to the type of microplastics found, they were mainly fibeours with lengths ranging between 100 and 250 µm in sediments and bivalves. Most of the microfibers found in the sediments were made of polyethylene terephthalate (PET) and polypropylene (PP), and the fibers found in the bivalves were made of PP.

In vitro bioaccessibility, phase partitioning, and health risk of potentially toxic elements in dust of an iron mining and industrial complex.

Dust emitted from mining, ore processing, and tailing dumps have direct effects on miners who work close to these operations. The Gol-E-Gohar (GEG) mining and industrial company is one of the most important iron concentrate producers in the Middle East. The objective of the present study was to estimate the distribution, fractionation, and oral bioaccessibility of potentially toxic elements (PTEs) in dust generated by the GEG mining and industrial company. Total PTE content including Al, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, V, and Zn was quantified for suspended particulate matter (PM) in PM2.5, PM10, and total suspended particulate matter (TSP). As, Cd, Co, Cu, Fe, Ni, and Pb were quantified in fallout dust samples for oral bioaccessibility using in vitro Unified BARGE (UBM) Method and modified BCR fractionation analysis. Enrichment factors (EF) were calculated for the studied elements in PM; Cu, Fe, and As were found to be extremely enriched. Oral bioaccessibility of selected PTEs in fallout dust samples ranged from 0.35% to 41.55% and 0.06-37.58% in the gastric and intestinal phases, respectively. Regression modeling revealed that the bioaccessibilities of the PTEs could mostly be explained by total concentrations in dust particles. Average daily intake (ADI) calculations revealed that the intake of PTEs did not exceed the tolerable daily intake (TDI) values and as such was not considered a significant risk to workers. Additionally, the hazard quotients (HQ) and carcinogenic risk (CR) values were lower than the acceptable level. This study can provide further risk assessment and management of PTE pollution in occupational environments.

Potentially toxic elements and polycyclic aromatic hydrocarbons in street dust of Yazd, a central capital city in Iran: contamination level, source identification, and ecological-health risk assessment.

Contamination level, source, and ecological-health risk of potentially toxic elements (PTEs) and polycyclic aromatic hydrocarbons (PAHs) in the street dust of Yazd, a central capital city in Iran, were investigated for the first time regarding samples collected from 21 sites. Geochemical indices pointed out an enrichment trend of [Formula: see text] and an ecological risk trend of [Formula: see text]. The ecological risk indices of PAHs reflected high ecological risk for pyrene (Pyr). The statistical approach along with the isomeric ratios of PAHs suggested that the traffic-related sources, such as wearing of tires and brake pads, and the vehicular exhaust emissions were greatly responsible for the elevated concentrations of Pb, Cu, Sb, and PAHs, while Al, Ni, Co, V, Mn, As, and, to a lesser extent, Fe, Zn, Mo, and Cr were mainly influenced by geogenic sources. The human health risk assessment of PTEs and PAHs reflected that As, Cr, and Pb pose the highest non-carcinogenic risk in adults and children, compared with other PTEs and also PAHs. The carcinogenic health risk of Pb in the children and PAHs in both subpopulations was high for cancer development.

Hydrogeochemical and ecological risk assessments of trace elements in the coastal surface water of the southern Caspian Sea.

This study investigates the occurrence, distribution, and potential ecological risk of trace elements (TEs) along with the hydrogeochemical characteristics of coastal surface water collected from the southern Caspian coasts in the Mazandaran province of Iran. Eighteen coastal water sites were sampled and analyzed using inductively coupled plasma-mass spectrometry and ion chromatography to determine concentrations of TEs and major ions, respectively. Mean concentrations (µg/l) of TEs in the water followed the order: Al (154.3) > Fe (73.6) > Zn (67.8) > Mn (29.9) > Cu (5.7) > Mo (3.7) > Cd (2.8) > Se (2.3) > V (1.9) > Co = As (1.8) > Sb (1.2) > Pb (0.6). TEs displayed high variations within samples, reflecting many sources that control their concentrations in the coastal water. Most TEs displayed elevated concentrations in the east and west of the study area. The Na-Cl water type in the majority of investigated sites indicates excess alkaline elements and strong acid anions relative to alkaline earth cations and weak acid anions. Considering the saturation states of minerals, carbonate and evaporite minerals are oversaturated and unsaturated in surface water, respectively. Compositional interrelations between aqueous species showed that reverse cation exchange may have occurred. The excess SO42- content, derived from irrigation return flow and domestic greywater, probably plays a crucial role in the mobilization and transport of Zn and Pb by binding to sulfate ligands and forming aqueous complexes. Ecological risk assessment of TEs revealed that water in the majority of sites is safe in terms of As, Se, Pb, and Cd content, and unsuitable with respect to Zn and Cu. Acute and chronic toxicities of Cu and Zn are reported in several sites, thus coastal water cannot be used for fishery and protecting "nature reserve" purposes. However, industrial activity and tourism are safe to be conducted in most coastal water sites.

Microplastic particles in sediments and waters, south of Caspian Sea: Frequency, distribution, characteristics, and chemical composition.

This study assesses the occurrence of microplastics (MPs) in coastal and sea surface sediments, as well as water samples, collected from the coastal region of the southern Caspian Sea, Mazandaran province, Iran. A total of 32 sediment and 10 water samples were studied. The mean concentration of MPs was 15 units kg-1 in the sediments and 710 units m-3 in the coastal water. Fibers constituted by far the dominant MPs in both media, accounting for 97% of the MPs in both sediment and water samples. The MPs were mainly black in color. The dominant size of MP particles in sediment samples was between 250 and 500 µm, while the fraction >1000 µm dominated in the water samples. Polyethylene terephthalate (PET), polystyrene (PS), and nylon (NYL) were the main polymers and/or copolymers composing MPs in both sediment and water samples. The MP particles had a relatively smooth surface morphology, although signs of weathering were observed. The number of MP particles in sediment and water samples showed a general decrease from west to east in the study area. This may be reflecting the spreading of MP loading from the outlets of Sefidrud, Tonekabon, Chalus, the major rivers entering the Caspian Sea just west of the study area, and the overall decrease in the spatial distribution of touristic and fishery activity. The main sources of MP particles could be local emissions from a large number of domestic wastewater effluents and urban surface runoff due to high population density, and industrial and fishing activities in this region. This study indicated that MP particles, based on their characteristics and chemical composition, are circulated between coastal waters, and shore and sea surface sediments of the Caspian Sea, leading to their uneven distribution in the different depths. To the best of our knowledge, this is the first work studying the distribution of MP particles in sea surface sediments and also the most comprehensive on MPs in shoreline sediments and coastal waters in the southern Caspian Sea.

Arsenic in the rock-soil-plant system and related health risk in a magmatic-metamorphic belt, West of Iran.

Following earlier reports of water contamination and arsenic (As) toxicity symptoms in residents of Kurdistan Province, As was determined in rock, soil and plant samples to investigate its fate from rock to crops and its potential effects on human health. Total As content ranged from 4.9 to 10,000 mg/kg, 7.7-430 mg/kg and < 0.05-25,079 µg/kg (dry weight) in rock, soil and plant samples, respectively. The Qorveh-Bijar region data indicated that magmatic differentiation has enriched late magmatic fluids in As. High rare earth elements concentration, dissociation coefficient, and positive Eu anomaly in volcanic rocks, indicated the prevalence of intermediate to felsic composition. The highest As concentration was measured in travertine. In soil, As average level in Qorveh and Bijar was 48.5 and 107 mg/kg, respectively. Higher pollution index and geoaccumulation index (Igeo) were also calculated for Bijar County. The As concentration in crop samples was greater than the recommended maximum permissible concentration for foodstuff. Mann-Whitney U test revealed significant differences between As concentration in different plant species and no difference between plants in Bijar and Qorveh. Also, alfalfa displayed the highest biological accumulation coefficient among the investigated plants. The calculated chronic daily intake of As in Bijar County was higher than the recommended levels for wheat and barley grains. Moreover, the hazard quotient (HQ) and incremental lifetime cancer risk assessments revealed high non-cancer (HQ > 1 for both adults and children) and cancer (particularly for barley in Bijar) risks for inhabitants via consumption of As contaminated crops cultivated in the study area.

Ecological-health risk assessment and bioavailability of potentially toxic elements (PTEs) in soil and plant around a copper smelter.

Soil and the dominant plant species in the vicinity of Khatoon Abad copper smelter in Kerman province of Iran are examined to determine contamination, bioavailability, and ecological-health risk of potentially toxic elements (PTEs) based on 23 collected soil samples and 13 Artemisia siebri plant species. Cu, Mo, As, and Sb display a significant level of enrichment in soil. Ecological risk assessment shows that Cu, As, and Cd pose the highest ecological risk. The results of PTEs fractionation reveal that, on average, Cu, As, Cd, Pb, Zn, and Mo are mostly distributed between non-residual fractions reflecting higher mobility and potential ecological risk, while Cr, Ni, and Co are significantly distributed within the residual fraction, and do not pose a serious ecological risk. Mobility factor suggests high bioavailability of Cu for plants followed by As, Cd, Pb, Mo, Co, Ni, and Cr. Biological accumulation coefficient displays higher phytoavailability of Mo and Cd. PTEs transfer within plant follows the order of Mo > As > Pb > Zn > Cu > Ni > Co > Cr > Cd. The results of phytoavailability indicate the high tendency of Cd to bioaccumulate in Artemisia's root, while Mo, As, and Pb tend to translocate towards Artemisia's shoot. Calculated hazard index and incremental lifetime cancer risk revealed that As poses the highest non-carcinogenic health risk, and As and Pb pose the greatest carcinogenic health risk in both adults and children.

Formation of Structured Membranes by Coacervation of Xanthan Gum with CnTAB Surfactants.

We present a novel approach for studying membrane formation by the interaction of polymers and surfactants with opposite charge using a Hele-Shaw experimental setup. A solution of the anionic biopolymer xanthan gum is placed in direct contact with a CnTAB surfactant solution (n = 10, 12, 14, and 16). Thereby, a polymer-surfactant membrane spontaneously forms between the two solutions due to the precipitation of polymer-surfactant complexes, which grows afterwards in the direction of the polymer solution. The dynamics of the growth of the membrane thickness and the mass transfer of polymer are evaluated for different surfactant types and concentrations. The experiments and supporting numerical calculations indicate that polymer mass transfer is driven by diffusion of the charged macromolecules along the concentration gradient, which is coupled to the electric field induced by the faster diffusion of the more mobile counterions. The properties and structure of the formed membrane significantly depend on the surfactant hydrophobicity and concentration. In addition, in a wide range of experiments, the formation of a porous structure in the membrane is observed whose characteristics can be tuned by the process parameters. A mechanism is proposed for the pore formation explaining it as an instability of the growing membrane surface in interaction with the supply of polymer across the depleted zone in the vicinity of the membrane front.

Potentially toxic elements (PTEs) and polycyclic aromatic hydrocarbons (PAHs) in fish and prawn in the Persian Gulf, Iran.

This study aimed to speciate and quantify potentially toxic elements (PTEs) and polycyclic aromatic hydrocarbons (PAHs), in addition to estimate potential human health risk of PTEs (As, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, Se, V, and Zn) through the consumption of three edible fish species (Leuciscus vorax, Liza abu, and Coptodon zillii) and two prawn species (Metapenaeus affinis and Penaeus semisulcatus) collected from Arvand River and Musa Estuary in the Persian Gulf. The concentration of As in prawn species exceeded permissible limit set by international organizations. PAHs were dominated by low molecular weight species such as naphthalene, phenanthrene, and, fluorene but generally exhibited low mean concentrations in fish and prawn samples. The human health hazard posed by PTEs was assessed using methods that consider estimated daily intake (EDI), estimated weekly intake (EWI), target hazard quotients (THQ), and combined THQ. The results suggested that elevated As concentrations in almost all prawn samples may pose a probable health hazard to local inhabitants.

Risk-based assessment of soil pollution by potentially toxic elements in the industrialized urban and peri-urban areas of Ahvaz metropolis, southwest of Iran.

The main purpose of this research was to assess the level of contamination, source identification, geochemical fractionation, and health risk of potentially toxic elements (PTEs) in industrial soils from urban and peri-urban areas of Ahvaz city. A total of 92 surface soil samples were gathered and concentrations of sixteen PTEs were measured using aqua regia digestion by an inductively coupled plasma mass spectrometry (ICP-MS). Possible sources of PTEs were quantitatively determined by positive matrix factorization (PMF) receptor model combined with geostatistical analyses and geochemical methods. The results showed that long-term industrial activities have enhanced the levels of some PTEs particularly Pb, Hg, Zn, Mo, Sb, Fe, Cu, and Cd to different extents. Contamination indices including geoaccumulation index, pollution index, and Nemerov integrated pollution index along with multivariate statistical analyses confirmed that steel and iron industries are the most contaminating industries in the study area. The outcomes attained from Kruskal-Wallis test affirmed that there was a significant difference among the concentrations of As, Hg, Mn, Cu, Fe, Pb, Mo, Cd, V, Zn, and Sb in soils around different industrial clusters. Among the studied elements, the highest mobility factors belonged to Zn (81.49%), Pb (76.71%), Cu (71.65%), Hg (66.23%), Mn (62.48%), and Mo (59.27%), respectively. Also, the PMF model showed that steel and iron industries (51.2%) and natural sources (23.4%) are the main sources of PTEs, followed by industrial towns (16.7%) and power plants (8.7%). This is in line with the results of principal component analysis (PCA). Majority of the measured PTEs showed the highest bioavailability in surface soils collected from around the steel and iron industries. Also, based on the outcomes of the health risk assessment model, particular attention should be paid to Hg, Pb, Zn, and Cu in industrial soils of Ahvaz.

Characteristics, distribution, source apportionment, and potential health risk assessment of polycyclic aromatic hydrocarbons in urban street dust of Kerman metropolis, Iran.

In this study, the concentrations of street dust-bound polycyclic aromatic hydrocarbons (PAHs) in Kerman metropolis as a typical arid urban area were determined to investigate the contamination, molecular composition, toxicity, and sources of PAHs. Sixteen individual PAHs on the United States Environmental Protection Agency priority list were analyzed using gas chromatography-mass spectrometry in street dust samples from 30 sites. ∑PAHs ranged between 165 and 5314.7 µg·kg-1 with a mean of 770.8 µg·kg-1. The most abundant individual PAHs were fluoranthene, phenanthrene, pyrene, and chrysene, respectively. High molecular weight PAHs (4-6 rings) made 74.8% of ∑PAHs mass and were dominant in all sites. Source apportionment was performed using ring classification, diagnostic ratios, and principal component analysis-multiple linear regression. The results indicated that primary contributors of PAHs in the street dust of Kerman could be liquid fossil fuel combustion, natural gas combustion, and petrogenic sources, accounting for 82.4%, 11.5%, and 6.1%, respectively. The calculated incremental lifetime cancer risk is 8.13 × 10-4 for children and 6.27 × 10-4 for adults. Hence, both children and adults in Kerman are potentially exposed to a high carcinogenic risk via ingestion and dermal contact.

Health risk assessment and source apportionment of polycyclic aromatic hydrocarbons associated with PM10 and road deposited dust in Ahvaz metropolis of Iran.

The objective of this study was to compare the characteristics of polycyclic aromatic hydrocarbons (PAHs) in PM10 and road dust samples, as well as to identify and quantify the contributions of each source profile using the positive matrix factorization (PMF) receptor model. Health risk assessment was carried out using toxic equivalency factors and incremental lifetime cancer risk (ILCR), which quantitatively estimate the exposure risk for age-specific groups. PM10 samples were collected on PTFE filters in the metropolitan area of Ahvaz. Road dust samples were also collected from all over the urban areas with different land uses. Total PAH concentrations in PM10 and road dust samples were 0.5-25.5 ng/m3 and 49.3-16,645 µg/kg, respectively. Pyrene was the highest PAH in the PM10 profile, whereas fluoranthene became the highest PAH in the road dust. Abundance of benzo[ghi]perylene at PM10 and road dust samples suggested a source indicator for traffic emissions. The results demonstrate that in 36.5% of samples, PM10 concentrations exceed the maximum concentration level recommended by EPA. A multiple linear regression model was used to estimate the influence of meteorological parameters (temperature, wind speed, and relative humidity) on buildup of PAHs. All of PAH species show higher concentrations during the cold and typical days rather than the dust event days and warm periods. PMF analysis showed that vehicular emissions (50.6%) and industrial activities (especially steel industries) (30.4%) were first two sources of PAHs bounded with PM10, followed by diesel emissions (11.6%) and air-soil exchange (7.4%). For road dust samples, three common sources were also identified: vehicular traffic (48%), industrial activities (42.3%), and petrogenic sources (9.7%), in line with that of diagnostic molecular ratios results. According to the results of health risk assessment model, the ILCR of exposure to PAHs associated with PM10 and road-deposited dust was higher than the guidelines of USEPA, indicating high carcinogenic risk.

Polycyclic aromatic hydrocarbons and potentially toxic elements in seafood from the Persian Gulf: presence, trophic transfer, and chronic intake risk assessment.

High bioavailability of man-made pollutants in marine environments raises serious concern regarding the safety of seafood. In the present study, the presence, trophic transfer, and risks of polycyclic aromatic hydrocarbons (PAHs), and potentially toxic elements (PTEs) in 170 benthic marine organisms (87 prawn; 28 crab; 55 fish) from the Persian Gulf were investigated. Among investigated species, E. coioides displayed the lowest level of metal pollution index (MPI), while P. armatus and P. semisulcatus showed the highest level of MPI and total PAHs, respectively. Principal component biplot exhibited a significant association of PTEs (except Hg) and PAHs in less motile benthic species. The results of trophic transfer investigation revealed that PTEs (except Hg) and PAHs were not biomagnified in the studied organisms through diet. However, Hg biomagnification factors greater than 1 indicated trophic transfer of mercury. In order to gain nutritional benefits of seafood, consumption of two fish/prawn meals/week for adults (except vulnerable groups such as pregnant women) and one fish/prawn meals/week for children is recommended. However, lifelong consumption of crabs (P. armatus) may threaten human health. In addition, the maximum allowable fish consumption rate (CRlim) for studied fish is 120 g fish/day for adults and 30 g fish/day for children. In the case of prawns, the safe dose is 30 and 10 g prawns/day for adults and children, respectively.

Polycyclic aromatic hydrocarbons (PAHs) in water and sediment of Hoor Al-Azim wetland, Iran: a focus on source apportionment, environmental risk assessment, and sediment-water partitioning.

The concentration, source, and ecological risk of 16 polycyclic aromatic hydrocarbons (PAHs) in water and sediment samples in Hoor Al-Azim wetland, a significant freshwater wetland in Lower Mesopotamia, were evaluated. Total PAHs concentrations varied from 15.3 to 160.15 ng/L, and 15.78 to 410.2 µg/Kg in water and sediment, respectively. PAHs pollution levels in sediments compared with sediment quality guidelines (SQG) were found to be moderate in two stations and low in water and the rest of sediment stations. Based on the diagnostic ratio analysis, cluster analysis (CA), and principal component analysis-multiple linear regression (PCA-MLR), the mean percentage contributions were 62.62% for mixed pyrogenic and petrogenic sources (e.g., unburned and combusted fossil fuels from fishing boats and vehicle engines, incomplete combustion, oil leakage), 20.68% for auto emission, and 16.7% for pyrogenic sources (fossil fuels and biomass combustion). According to the sediment risk assessment indices such as mean effects range-median quotient (M-ERM-Q), the ecological risk of multiple PAHs was low. Risk quotient (RQ) calculation of water samples suggested high ecological risk level for Benzo[a]anthracene (BaA), and low to moderate for other individual PAHs and ΣPAHs. The result of PAHs partitioning between sediment and water phases revealed that most PAHs prefer to accumulate in sediment. Sediments probably act as a secondary source for some PAHs in the oil collection and pumping station.