Anthropogenic Sources Research Articles

THE ECOLOGICAL ASSESSMENT OF SMALL RIVERS IN UKRAINE UNDER CONDITIONS OF INTENSIVE WAR IMPACT

Aquatic ecosystems are perpetually exposed to anthropogenic sources of pollution, wherein the quality of subterranean and surface waters undergoes influence from both natural and anthropogenic processes. This interaction results in environmental predicaments and, occasionally, environmental crises. Small rivers, in particular, bear a pronounced impact from human interventions on the environment. The investigation undertaken by the researchers commenced in 2021 with the primary objective of scrutinizing the ecological condition of the Irsha River. Regrettably, due to the military aggression of the Russian Federation, the regions through which the river courses were temporarily occupied, subjecting it to considerable anthropogenic disturbances. Specifically, two bridges spanning the Irsha River in the Malyn area were demolished, and military operations transpired along the riverbanks, leading to the accumulation of damaged military equipment. Consequently, it was deemed imperative during the course of our study to conduct an analysis of the natural water in the Irsha River subsequent to the military activities. The outcomes of a comprehensive assessment of surface water quality, employing a graphical method, revealed that, during the period of 2021-2022, the river waters within the Irsha River exhibited an overall failure to meet quality standards in both monitoring locations. Elevated values of Maximum Permissible Concentration (MPC) exceeding the norm were noted for the Chemical Oxygen Demand (COD) indicator, the dissolved oxygen indicator, as well as the general iron and iron of permanganate oxidizability parameters in both samples. The highest degree of pollution was discerned in the Malyn Reservoir, whereas the Irsha Reservoir manifested comparatively lower pollution levels in the aquatic environment.

Hazard profiles, distribution trends, and sources tracing of rare earth elements in dust of kindergartens in Beijing

Children, the most vulnerable group in urban populations, are susceptible to the effects of pollution in urban environments. It is significant to evaluate the influence of rare earth elements (REEs) from kindergartens dust (KD) in Beijing on children's health. This study collected surface dust from 73 kindergartens in 16 districts of the mega-city of Beijing, and the concentrations of 14 REEs in KD, including La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, were detected. The contamination levels, source apportionment, and health exposure risk of REEs were comprehensively investigated. The results indicate that the contamination levels of 14 REEs are within the acceptable range. Nevertheless, Eu, Ce, La, Pr, Nd, Gd, and Sm show high enrichment due to anthropogenic influence. Besides, KD is rich in light rare earth elements (LREEs) (90.97 mg kg−1) compared to heavy rare earth elements (HREEs) (8.65 mg kg−1). The distribution parameter patterns of REEs suggest that complicated anthropogenic sources influence the enrichment of REEs in KD. The main sources of REEs in KD include natural sources (40.64%), mixed high-tech industries and construction (33.89%), and mixed coal-fired, historical industrial, and transportation sources (26.47%). The primary pathway for daily intake of REEs in children is through ingestion, which presents a low but not negligible health risk. This study provides guidance for the effective risk management of REEs in KD.

Source and fate of atmospheric iron supplied to the subarctic North Pacific traced by stable iron isotope ratios

The availability of dissolved iron (Fe) limits primary production over some regions of the surface ocean, especially in regions such as the subarctic North Pacific. In this work, we use Fe stable isotope ratios (δ56Fe) in bulk and size-fractionated marine aerosol particles and dissolved Fe of surface seawater in the subarctic North Pacific on Japanese GEOTRACES cruise GP02 (Summer 2017) as a tracer to clarify the relative contribution of combustion and natural Fe in both marine aerosol particles and surface seawater. The bulk aerosols collected in the coastal regions of both East Asia and western North Pacific have total δ56Fe values that are as low as −0.5 ‰ when compared to crustal (+0.1 ‰), with both the water-soluble phase and the fine particles even more fractionated (as low as −1.9 and −2.8 ‰, respectively). The negative correlation between the aerosol δ56Fe signatures and the enrichment factors of Fe and other elements dominated by anthropogenic sources (e.g., lead and cadmium) in these coastal regions indicates the presence of Fe emitted from high-temperature combustion sources, such as coal combustion and metal smelting. In these regions, combustion Fe accounts for 4–13 and 13–45 % of the total and water-soluble aerosol Fe, respectively. The results demonstrate that soluble aerosol Fe sourced from combustion Fe can be equivalent to that sourced from natural dust Fe in these coastal regions. By contrast, the aerosol particles in pelagic regions were near crustal δ56Fe in all particle size fractions, indicating the dominance of natural Fe and little to no combustion Fe. The relationships among the fractional Fe solubility, major ion concentration, Fe species, and δ56Fe indicate that the presence of combustion Fe is the dominant reason for the solubility increase in the coastal regions and that the atmospheric processing of mineral dust during transport is more important in the pelagic regions. The dissolved Fe of the surface seawater at 10 m depth had a consistently higher δ56Fe by up to +1.5 ‰ than that of the simultaneously collected water-soluble aerosol Fe. The pattern of the elevated δ56Fe in the surface seawater corresponds to decreasing Fe concentrations and can be approximated by Rayleigh fractionation; we attribute these elevated surface δ56Fe values to the effect of biological uptake. New Fe fluxes from both the atmosphere and deeper depths are limited at least in summer compared with the biological uptake in the open ocean of the subarctic North Pacific.

Spatiotemporal variations of atmospheric mercury at urban and suburban areas in Southern Vietnam megacity: A preliminary year-round measurement study

Atmospheric mercury (Hg) pollution studies in peninsular Southeast Asia (PSEA) are currently experiencing shortage on spatiotemporal coverage due to limited observation data. Therefore, our study provided year-round (May 2022–April 2023) atmospheric Hg data at two urban and one suburban site in Ho Chi Minh City (HCMC) Vietnam - a megacity in PSEA. Higher total gaseous Hg (TGM) levels at 2 urban sites of 2.49 ± 0.86 ng m−3 (Nguyen Van Cu) and 2.12 ± 0.49 ng m−3 (Linh Trung) were observed as compared to the suburban site of 1.76 ± 0.50 ng m−3 (Can Gio) which suggests the influence of anthropogenic Hg sources. Higher TGM concentration in October 2022–January 2023 as opposed to May 2022–September 2022 at all 3 sites reflected the influence of abrupt change in air mass origins and transport pathways in southern Vietnam. Backward trajectories (BWTs) and concentration-weighted trajectory (CWT) models further suggested East Asian outflow from northeast (NE) direction as a prominent TGM source in HCMC. Our two case studies in June and December 2022 helped to distinguish the impacts of local accumulation besides long-range atmospheric Hg transport towards TGM levels in HCMC. We also attempted to address TGM public health concerns wherein a minimal hazard quotient (HQ < 1) implied insignificant Hg health risk via inhalation pathways. Our study strives to offer crucial information to fill the Hg data gap as well as seeks to explore the impact of monsoon drives on Hg pollution in the PSEA region.

Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China

Abstract. While aqueous-phase processing is known to contribute to the formation of nitrogen-containing organic compounds (NOCs), the specific pathways involved remain poorly understood. In this study, we aimed to characterize the NOCs present in both pre-fog aerosols and fog water collected at a suburban site in northern China. Fourier-transform ion cyclotron resonance mass spectrometry was utilized to analyze the molecular composition of NOCs in both negative and positive modes of electrospray ionization (ESI− and ESI+). In both pre-fog aerosols and fog water samples, NOCs constituted a significant portion, accounting for over 60 % of all assigned formulas in ESI− and more than 80 % in ESI+. By comparing the molecular composition of NOCs originating from biomass burning, coal combustion, and vehicle emissions, we identified that 72.3 % of NOCs in pre-fog aerosols were attributed to primary anthropogenic sources (pNOCs), while the remaining NOCs were categorized as secondary NOCs formed within the aerosols (saNOCs). Unique NOCs found in fog water were classified as secondary NOCs formed within the fog water (sfNOCs). Through a comprehensive “precursor–product pair” screening involving 39 reaction pathways, we observed that the nitration reaction, the amine pathway, and the intramolecular N-heterocycle pathway of NH3 addition reactions contributed 43.6 %, 22.1 %, and 11.6 % of saNOCs, respectively. In contrast, these pathways contributed 26.8 %, 28.4 %, and 29.7 % of sfNOCs, respectively. This disparity in formation pathways is likely influenced by the diverse precursors, the aqueous acidity, and the gas-phase species partitioning. Correspondingly, saNOCs were found to contain a higher abundance of carbohydrate-like and highly oxygenated compounds with two nitrogen atoms compared to pNOCs. Conversely, sfNOCs exhibited a higher content of lipid-like compounds with fewer oxygen atoms. These results underscore the distinct secondary processes contributing to the diversity of NOCs in aerosols and fog water, which may lead to their different climate effects.

Quantitative evaluation of anthropogenic sources and health risks of rare earth elements in airborne particulate matter

Rare earth elements (REEs) have emerged as contaminants in airborne particulate matter (PM); however, their anthropogenic sources remain poorly quantified, and associated health risks are unknown. This study investigates the REE distribution across eight sizes of airborne PM during July and December in Qingdao, a major Chinese port city. Our results reveal a single coarse-mode distribution with REE concentrations. In contrast, fine PM (size: 0.43–2.1 μm) exhibits notable enrichment of La and Ce compared to Al and other REEs. This study traces La and Ce enrichment to fluid catalytic cracking catalysts (FCCC)-related sources, including refinery and ship emissions, by comparing the REE fractionation in samples with potential sources. We quantify the contributions from FCCC-related sources to La (July: 33.6 % ± 3.2 %, Dec.: 46.4 % ± 5.2 %) and Ce (July: 16.5 % ± 14.3 %, Dec.: 30.3 % ± 12.2 %) by comparing measured concentrations with predictions derived from neighboring REEs, a method previously used exclusively in aquatic systems. For the first time, supply ratios of refinery and ship to FCCC-related La are calculated using a two-component mixing model based on the [La]FCCC/[V]anth, revealing the dominance of refinery emissions (July: 97.3 % ± 0.6 %, Dec.: 99.6 % ± 0.1 %). Furthermore, a global review of La and Ce anomalies that integrates published REE data with our findings reveals a widespread distribution of positive anomalies. The significantly positive correlation between La and Ce anomalies underscores FCCC-related emissions as a global source in fine PM, contributing 0–92 % (mean: 35 % ± 33 %) for La and 0–72 % (mean: 21 % ± 24 %) for Ce. Although the non-carcinogenic health risks of Ce are generally low globally, concerns should be raised in areas near source emissions, where Ce health risks sharply increased along with its concentrations. There is urgently need to establish a threshold value for La, owing to its global enrichment. This study provides novel insights into the sources and health implications of REEs in airborne PM.

Natural radioactivity in food crops and soil and estimation of the concomitant dose from tin mining areas in Nigeria

Mining of mineral ore is considered one of the anthropogenic sources of elevating the activity concentrations of the natural radionuclides in the environment, which in turn causes an increased risk of human exposure via the food chain. In an attempt to evaluate the radiological burdens resulting from tin mining activities in Nigeria, farm soil and sixty-two samples of different food crops grown around tin mining areas were evaluated for the activity concentrations of 226Ra, 232Th, and 40K using a high-purity germanium detector. The mean activity concentrations of 226Ra, 232Th and 40K in soil were 64.6 ± 29.5, 72.03 ± 28.73 and 680.6 ± 324.3 Bq/kg, respectively. These values were found to be higher than their corresponding world average values. However, the mean activity concentrations of the measured radionuclides in plants were below their respective world average values, as reported by UNSCEAR. The overall average annual ingestion dose due to the consumption of the analysed plants was 151 µSv/y, which is below the reported world average value of 290 µSv/y. The results obtained show that the hazard indices were low enough to cause any immediate radiological health complications due to the ingestion of the crops grown in the studied areas.

Occurrence, transport and sources of metals and metalloids in the Bangpakong River in the eastern economic corridor area of Thailand

The occurrence of elements in river water is affected by various factors, including mobility, weathering and transport processes and anthropogenic contributions. A total of six water sampling campaigns were conducted from 2021 to 2022 to study the factors affecting the occurrence of twelve elements (Al, As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Zn and Se) in the Bangpakong River. The total concentrations of all the elements were within the levels set by the national surface water quality standard. Comparisons of dissolved elemental concentrations in the study area with the global average for dissolved elemental concentrations in pristine rivers indicated contamination with Al, As, Co, Mn, Zn and Se in the river water. Based on the percentage of each element in particulates to the total concentration, Al (80.6 %), Cr (71.9 %), Cu (69.9 %), Fe (95.6 %), Mn (76.6 %), Pb (74.7 %), and Zn (70.6 %) were mainly transported in the particulate phase in both the dry and wet seasons. However, As (65.5 %), Co (60.3 %), and Se (77.6 %) were mainly transported in the dissolved phase in both seasons. The ratios of the dissolved Se concentration in river water to the Se concentration in the Earth's crust indicated significant and high mobility, especially in downstream sites, likely due to Se leaching from alluvial sediments. Seawater intrusion is likely the cause of As and Zn contamination in the dry season. Weathering of rocks and soils likely causes Al, Co, and Mn contamination in the wet season. The anthropogenic sources of contamination include the discharge of Mn and Zn from fertilizers in agriculture and the use of formulated feed in aquaculture. Approximately 52.98, 25.23, 5.68 and 0.63 tons of Fe, Al, Mn and Zn, respectively, are estimated to be transported from the river into the Gulf of Thailand each year.

Occupational and human health risks of exposure to potentially toxic elements (PTEs) in top soils from steel fabrication workshops

IntroductionEnvironmental pollution caused by potentially toxic elements (PTEs) from anthropogenic sources has become a global concern due to its deleterious effect on humans and ecosystem health. Therefore, this study evaluated the concentrations of PTEs, pollution level and human health risk in topsoil from ten (10) steel fabrication workshops in Abeokuta, Ogun State, Nigeria. Materials and methodsTen (10) composite soil samples were collected in November 2023, from 10 different steel fabrication workshops in proximity to residence in Abeokuta, Ogun State, Nigeria. One (1) gram of processed sample was digested using aqua regia and PTE concentration estimated using atomic absorption spectrophotometer (AAS). Pollution index assessment was determined using enrichment factor (EF) and geo-accumulation index (I-geo) while descriptive statistics and correlation were subjected to statistical package for social sciences (SPSS). ResultsThe result showed that Iron (Fe) (11,500 – 42,100 mg kg−1), Lead (Pb) (10.7 – 583 mg kg−1), Chromium (Cr) (16.3 - 49.7 mg kg−1), Zinc (Zn) (34.6 – 343 mg kg−1), Manganese (Mn) (109 – 840 mg kg−1), Nickel (Ni) (2.23 - 25.3 mg kg−1), Copper (Cu) (16.6 -107 mg kg−1) and Cadmium (Cd) (2.23 - 25.3 mg kg−1) were present. Mean concentration for Pb (179±202 mg kg−1) is higher than the Canada soil guideline value (CSGV) (140 mg kg−1) while other PTEs are within the recommended limit. Pollution indices revealed EF (Cd and Pb) and I-geo (Cd) as the primary pollutants in the soil while the strong significant correlation between Cr, Cu and Mn p < 0.05. Cr, Ni, Pb and that of Cu, Mn, Ni, Pb, Zn p < 0.01 suggest an emanation from both geogenic and anthropogenic sources. Human health risk assessment revealed Fe as the most dosed PTE and ingestion as the major pathways of exposure especially to children being the most susceptible. Hazard index (HI) and total cancer risk (TCR) values for PTEs were <1 and within the acceptable threshold (1 × 10−6 – 1 × 10−4) except for Pb (3.93E+01; 1.16E-03) in adults respectively. ConclusionThe study showed that the topsoil from the steel fabrication workshop is polluted with Pb and Cu toxicity and the adult (residents and workers) population exposed to the soil is potentially at a non-cancer and cancer risk.

Origin and comprehensive risk assessment of heavy metals in surface sediments along the Caspian Sea

Metal concentrations (Cu, Zn, Cr, Fe, As, Pb, Ni, V, and Co) in surface sediments were determined in the southern Caspian Sea. Sediment pollution was investigated using geochemical index such as Enrichment Factor (EF) and ecological risk indices like modified Hazard Quotient (mHQ) and Toxic Risk Index (TRI). The highest calculated geochemical index was observed in sediments near the cities of Chalus and Ramsar, which are highly polluted due to human activities. The ecological potential indices indicated that Ni contents in all the studied stations would impose harmful effects on aquatic organisms, while other metals had a low risk. Principal component and cluster analyses suggested that As and Pb emanated from anthropogenic sources, and other metals probably originated from lithogenic sources.

Investigating the influence of particle hydrophobicity on lung deposition using nonionic dye partitioning

The regional deposition of inhaled particulate matter (PM) in the respiratory tract determines its biological fate and lung toxicity. While it is widely accepted that the size of PM plays a predominant role in affecting lung deposition, the impact of other physicochemical properties, especially hydrophobicity, remains unclear. This knowledge gap exists, in part, due to the absence of standard methods to characterize the hydrophobicity of PM. Here, we developed a novel nonionic dye partitioning method to quantitatively characterize the hydrophobicity of PM. The use of a nonionic dye, rhodamine B, effectively eliminates experimental artifacts arising from unwanted dye adsorption due to electrostatic interactions, thus significantly improving the accuracy and applicability of the method. Through an intranasal mouse exposure model, we discovered that the lung deposition of four types of PM originated from common anthropogenic sources, including PM2.5, dust, biochar, and carbon black, is mediated by their hydrophobicity. The most hydrophobic PM tends to be trapped in the nasal cavity, whereas the least hydrophobic PM penetrates deep into the alveoli, inducing severe lung inflammation. The hydrophobicity-dependent deposition of PM in the respiratory tract offers novel insights into understanding the acute lung toxicity of inhaled PM and provides a foundation for the design of safer and more efficacious inhalable medicines. Furthermore, the nonionic dye partitioning method shows promise as a user-friendly and cost-effective approach for characterizing the hydrophobicity of PM.

Effects of VOC emission reduction on atmospheric photochemistry and ozone concentrations during high-ozone episodes

We studied atmospheric volatile organic compounds (VOCs) characteristics and sources during fifteen high ozone (O3) episodes (daily 1-h maximum >100 ppbv and maximum 8-h average > 80 ppbv) in Nanjing, China, and used a photochemical box model to study the O3 formation sensitivity of VOCs, O3 photochemistry, radical budget, and reactivity for different emission reduction scenarios together with the base case ones. Overall, emission reduction from biogenic sources, followed by combustion sources, multiple sources, and solvent usage, had the major impacts on the O3 concentrations. According to photochemical box model simulations, isoprene was the most sensitive or influential VOC in the formation of O3, followed by ethylene, o-xylene, and cis-2-pentene. A 20.6 ± 11.7% concentration reduction of the sixteen most sensitive VOCs (SV16) for the production of O3 could bring the O3 concentration below the national standard level (daily 1-h maximum <100 ppbv). Besides, a 30% emission reduction from all the anthropogenic sources was more than enough to bring the O3 concentration below the national standard level. The total emission reduction of alkenes was always enough to bring the O3 concentration below the national standard level, which was not the case for aromatics under severe pollution conditions. The simulated OH reactivity analysis illustrates the importance of alkenes and aromatics, which account for about half of the total OH reactivity. The highest OH reactivity decreased due to the emission reduction for biogenic sources, followed by combustion and multiple sources. Alkenes played a major role in the OH, HO2, and RO2 radical's formation in the study area. The biggest drop in OH, HO2, and RO2 radical concentrations was noticed for biogenic emission reduction, followed by combustion and multiple sources. Due to the emission reduction from VOC sources, the highest O3 formation rates decreased for biogenic sources, followed by combustion and multiple sources. The acquired information is valuable to the scientific community and policymakers for formulating and implementing O3 pollution control strategies.

Maximising ecological value and assessing land suitability for sustainable grassland management in Asia’s largest tropical grassland, Western India

Grasslands are crucial ecosystems that provide numerous ecological services and support biodiversity conservation. Grasslands undergo significant threats from both anthropogenic and natural sources, compromising their ability to maintain biodiversity, ecosystem services, and human well-being. However, grasslands are frequently ignored in sustainable development objectives. Adequate knowledge of how grassland degradation affects ecosystem services is essential for sustainable management and grassland ecological restoration. The Kachchh region in western India harbours a unique grassland ecosystem known as the Banni grassland, which once became the finest grassland in Asia. However, undesirable anthropogenic interventions have accelerated its degradation. This research paper aims to assess the suitability of different land areas in Banni for sustainable grassland restoration, considering ecological value as a primary criterion. In the present research, land suitability for grassland management was assessed using a geographical information system (GIS)-based multi criteria evolution (MCE) method with satellite data and the analytic hierarchy process (AHP). The ground truthing of the soil samples was carried out alongside. Slope, rainfall, infiltration rate, LULC, geomorphology, soil texture, soil organic carbon, water holding capacity, SAR, CEC, pH, EC, and soil nutrients were among the criteria used. The weights for each criterion were calculated using a pairwise comparison matrix, and the scores were allocated to sub criteria based on field work, expert opinions, and a literature review. The proposed method can be very useful for evaluating the state of the land and can help with the best possible planning for grassland development and conservation. Banni grassland has the potential to be developed into a critical zone observatory (CZO) in the future, and the present study, with further inputs, holds promise for furthering the cause of its sustainable management. Overall, this study underscores the importance of assessing land suitability for sustainable grassland management and highlights the potential for maximising the ecological value of grasslands in western India and beyond.

Elemental Analysis of Five Medicinal Plants Species Growing in North Ossetia Using Neutron Activation Analysis

One important category of traditional remedies is medicinal plants, which are widely consumed by the population and often subjected to contamination. For the first time, the elemental composition of five wild medicinal plants traditionally consumed in the Republic North Ossetia—brook-mint (Mentha longifolia), oregano (Origanum vulgare), St. John’s wort (Hypеricum perforаtum), thyme (Thymus daghestanicus), and fireweed (Chamaenerion angustifolium)—and corresponding soil samples was determined. This investigation aimed to assess the degree of toxic element accumulation in plants and the possible toxic effect of the analyzed plants on human health. The analysis encompassed the quantification of 36 major and minor elements in soil samples, alongside the detection of 23 elements in plant samples using instrumental neutron activation analysis. According to contamination and enrichment factors, which were calculated in order to assess the level of soil pollution, elements such as As, Sb, Zn, and U in soil may originate from both geogenic and anthropogenic sources. In all plant samples, the most abundant major elements were K and Ca and their content ranged from 9870 to 49,500 mg·kg−1 and 5400 to 20,000 mg·kg−1, respectively, while among the microelements, Fe (54–2080 mg·kg−1) and Mn (27.8–190 mg·kg−1) can be highlighted as the most abundant. The transfer factor was calculated to estimate metal uptake from soil in plants. The highest values of the transfer factor were obtained for Mo, K, Ca, and Zn. The daily intake of metals and the health risk index were calculated to assess the safety of the collected plants. The health risk index was below the threshold for all plants suggesting a probable non-carcinogenic effect. Principal component analysis and linear discriminant analysis were used as classification techniques. The principal component analysis allowed us to define the main groups of elements and associate them with their sources of origin, while discriminant analysis enabled us to discriminate plant samples by species.

Distribution Characteristics and Assessment of Heavy Metal Pollution in Sediments of Fengyuan River, Guangdong

Mining activities and industrial production discharges often generate heavy metal pollution and pose serious environmental impacts. It is of great significance to study the pollution status and sources of heavy metals in polluted rivers for environmental pollution control. This paper determines the concentration of 34 heavy metals, including As, Cd, Cr, Cu, Ni, Pb, and Zn, in the Fengyuan River and tailing pond in Yunfu City, Guangdong Province. The potential ecological risk index (RI) and integrated pollution index (IPI) were used to evaluate the spatial distribution and pollution levels of heavy metals, and the possible source and enrichment of heavy metal were identified and assessed using enrichment factor (EF). The results showed that Cd and Tl in the slag of the tailings pond were the most serious; The potential ecological risk index indicates that Cd in the sediment of the Fengyuan River is a very severe ecological risk, As and Pb caused heavy and moderate ecological risk, respectively, while, Co, Cr, Cu, Mn, Ni, V, and Zn constituted mild ecological risks; The integrated pollution index shows that all the sampling sites are above high pollution. The average enrichment factor of Cd in surface sediments reached 28.11. The EF values of As, Cu, Mn, Pb, and Zn were all greater than 1. The RI, IPI, and EF produced similar levels of heavy metal pollution in sediments, thereby confirming each other’s results, indicating that the Fengyuan River is heavily contaminated, and As, Cd, Mn, Pb, and Zn were likely to have an effect on the aquatic ecosystem. According to principal component and hierarchical cluster analyses, the Fengyuan River may contain heavy metals from a variety of sources, such as tailings ponds, industrial parks, chemical effluent, and more. In addition, correlation analysis indicates that total organic carbon is significantly correlated with the concentrations of As and Cr, respectively, and combining EF suggests that cluster 1 containing As, Mn, and Pb and cluster 2 containing Cd and Zn may be derived from similar anthropogenic sources. This study can provide meaningful basic information for environmental development planning and decision-making associated with human health in the region.

Airborne particle radioactivity during desert dust days in Cyprus

Mediterranean countries are often affected by desert dust storms, which have significant effects on the environment and public health. We compared airborne particle radioactivity levels during desert dust and non-dust days in Cyprus.Gross α- and β-radioactivity from Total Suspended Particle (TSP) samples, collected at two urban routine monitoring stations in Limassol and Nicosia, were available for the period 2017–2020 and 2008–2020, respectively. Radionuclides 137Cs and 40K, from TSP samples, were also available from a semi-industrial monitoring station in Nicosia during 2008–2020. Information on desert dust presence, dust origin, particulate matter (PM) levels, and solar activity (KP index and solar sunspot numbers - SSN) were also obtained. We used linear regression models adjusting for seasonality and long-term trends, and solar activity to assess the effect of dust storms on TSP gross α- and β-, and 137Cs and 40K radioactivity levels.Gross α- and β-radioactivity, and 137Cs and 40K radioactivity levels were significantly higher on days with desert dust compared to days characterized with no influence of desert dust. Levels of gross α- and β-radioactivity during dust days were higher when dust originated from the Middle East deserts than from the Sahara Desert. The same trend was observed for the ratios 137Cs to 40K and 137Cs to PM10. Conversely, ratios of TSP gross α- and β-radioactivity to PM10 were significantly lower during desert dust days in comparison to days without dust influence.This study suggests that desert dust increase both TSP gross α- and β-radioactivity, as well as 137Cs and 40K radioactivity levels. Further studies should clarify the contribution of anthropogenic and other natural sources to the emission or transportation of particles radioactivity, to better mitigate future exposures.

Low mercury risks in paddy soils across the Pakistan

Mercury (Hg) is a globally distributed heavy metal. Here, we study Hg concentration and isotopic composition to understand the status of Hg pollution and its sources in Pakistan's paddy soil. The collected paddy soils (n = 500) across the country have an average THg concentration of 22.30 ± 21.74 ng/g. This low mean concentration suggests Hg pollution in Pakistan was not as severe as previously thought. Meanwhile, samples collected near brick kilns and industrial areas were significantly higher in THg than others, suggesting the influence of Hg emitted from point sources in certain areas. Soil physicochemical properties showed typical characteristic of mineral soils due to the study area's arid to semi-arid climate. Hg stable isotopes analysis, depicted mean Δ199Hg of −0.05 ± 0.12‰ and mean δ202Hg −0.45 ± 0.35‰, respectively, for contaminated sites, depicting Hg was primarily sourced from coal combustion by local anthropogenic sources. While uncontaminated sites show mean Δ199Hg of 0.15 ± 0.08‰, mean Δ200Hg of 0.06 ± 0.07‰ and mean δ202Hg of −0.32 ± 0.28‰, implying long-range transboundry Hg transport through wet Hg(II) deposition as a dominant Hg source. This study fills a significant knowledge gap regarding the Hg pollution status in Pakistan and suggests that the Hg risk in Pakistan paddies is generally low.

First measurements of chlorine 36 (36Cl) wet deposition fluxes in the vicinity of Orano La Hague nuclear reprocessing plant in France

Chlorine 36 (36Cl) is a radionuclide of natural and anthropogenic origin, mainly used as a tracer in geochemical studies. Owing to analytical constraints and its low environmental levels, knowledge of 36Cl behavior in the environment is still very limited. In this study, we use environmental measurements to report for the first time the wet deposition fluxes of 36Cl downwind an anthropogenic source, the Orano nuclear reprocessing plant, which chronically emits 36Cl into the environment. Measurements of 36Cl in rainwater samples at our study site were 1–2 orders of magnitude above the environmental background. The isotope ratios 36Cl/Cl of the samples and the 36Cl content in the rainwater averaged 2.3x10−12 at at−1 and 1.7x108 at l−1 respectively. A decrease in these levels was observed 20 km away from the study site, outside the plant's gas plume, indicating that the marking of 36Cl on the study site is related to the plant discharges. Over the sampling period, wet deposition fluxes at the study site averaged 3.4x103 at m−2s−1, with significant values measured when precipitations scavenge the plant's gas plume down onto our study site. Analysis of these fluxes also revealed the presence of a significant rainout phenomenon in the study area. These results provide new data on the wet deposition flux of 36Cl and will thus enable better assessment of impact studies in a context of decommissioning or accidents involving nuclear power plants.

Characterization of the inhalable fraction (< 10 μm) of soil from highly urbanized and industrial environments: magnetic measurements, bioaccessibility, Pb isotopes and health risk assessment

Soil in urban and industrial areas is one of the main sinks of pollutants. It is well known that there is a strong link between metal(loid)s bioaccessibility by inhalation pathway and human health. The critical size fraction is < 10 μm (inhalable fraction) since these particles can approach to the tracheobronchial region. Here, soil samples (< 10 μm) from a highly urbanized area and an industrialized city were characterized by combining magnetic measurements, bioaccessibility of metal(loids) and Pb isotope analyses. Thermomagnetic analysis indicated that the main magnetic mineral is impure magnetite. In vitro inhalation analysis showed that Cd, Mn, Pb and Zn were the elements with the highest bioaccessibility rates (%) for both settings. Anthropogenic sources that are responsible for Pb accumulation in < 10 μm fraction are traffic emissions for the highly urbanized environment, and Pb related to steel emissions and coal combustion in cement plant for the industrial setting. We did not establish differences in the Pb isotope composition between pseudo-total and bioaccessible Pb. The health risk assessment via the inhalation pathway showed limited non-carcinogenic risks for adults and children. The calculated risks based on pseudo-total and lung bioaccessible concentrations were identical for the two areas of contrasting anthropogenic pressures. Carcinogenic risks were under the threshold levels (CR < 10–4), with Ni being the dominant contributor to risk. This research contributes valuable insights into the lung bioaccessibility of metal(loids) in urban and industrial soils, incorporating advanced analytical techniques and health risk assessments for a comprehensive understanding.

Heavy metal pollution indices in soil and plants within the vicinity of the Gosa Dumpsite in Abuja, Nigeria.

Heavy metal contamination in the soil and phytoremediation potential of the plants cultivated around the Gosa dumpsite were evaluated using pollution indices. The concentrations of heavy metals in the soil and plant samples were determined using an atomic absorption spectrophotometer (Agilent 280FS AA). The mean heavy metal contents in the upper and lower soil layers ranged from 0.37 to 1662.61mg/kg and 0.32 to 1608.61mg/kg, respectively, in ascending order of Cd < Cr < Cu < Ni < Pb < Co < Zn < Fe. The results revealed a steady depthwise decrease in heavy metal contents from the upper to lower soil layers. Co, Pb, Zn and Fe were introduced through geogenic and anthropogenic pathways, while Cr, Ni, Cu and Cd were derived mainly from anthropogenic sources. The mean soil enrichment in the heavy metals ranged from 0.96 to 237.04 in the ascending order of Fe > Co > Pb > Zn > Cu > Cd > Cr > Ni. The soil was moderately polluted with Co, Cu, Pb, Zn, Fe and Cd but heavily polluted with Cr and Ni. The results revealed that 37.5% of the sites studied had pollution load indices greater than 1.0, indicating gradual deterioration in overall soil quality. The concentrations of Pb, Cd and Fe exceeded the recommended limits for the five plant species assessed. The transfer factor (TF) values of okra plant 1 (0.7536), water hyacinth (1.3768), and Amaranthus hybridus (0.9783) indicated excellent Cd phytoremediation potential. Okra Plant, water hyacinth and Amaranthus hybridus had excellent potential for phytoremediation of Cu, Fe and Pb, respectively. The study area was strongly enriched in Fe, Cd, Cr, and Ni, suggesting some degree of soil pollution, while the plants demonstrated an excellent capacity to accumulate Cd, Cu, Fe and Pb. This dumpsite should be adequately monitored while proper remediation measures are adopted by government authorities.