Sources Of Metals Research Articles

Source and Migration Pathways of Heavy Metals in Soils from an Iron Mine in Baotou City, China

Source and Migration Pathways of Heavy Metals in Soils from an Iron Mine in Baotou City, China

Metal impact and vaporization on the Moon's surface: Nano‐geochemical insights into the source of lunar metals

AbstractMillimeter‐to‐nanometer‐sized iron‐ and nickel‐rich metals are ubiquitous on the lunar surface. The proposed origin of these metals falls into two broad classes which should have distinct geochemical signatures—(1) the reduction of iron‐bearing minerals or (2) the addition of metals from meteoritic sources. The metals measured here from the Apollo 16 regolith possess low Ni (2–6 wt%) and elevated Ge (80–350 ppm) suggesting a meteoritic origin. However, the measured Ni is lower, and the Ge higher than currently known iron meteorites. In comparison to the low Ni iron meteorites, the even lower Ni and higher Ge contents exhibited by these lunar metals are best explained by impact‐driven volatilization and condensation of Ni‐poor meteoritic metal during their impact and addition to the lunar surface. The presence of similar, low Ni‐bearing metals in Apollo return samples from geographically distant sites suggests that this geochemical signature might not be restricted to just the Apollo 16 locality and that volatility‐driven modification of meteoritic metals are a common feature of lunar regolith formation. The possibility of a significant low Ni/high Ge meteoritic component in the lunar regolith, and the observation of chemical fractionation during emplacement, has implications for the interpretation of both lunar remote‐sensing data and bulk geochemical data derived from sample return material. Additionally, our observation of predominantly meteoritic sourced metals has implications for the prevalence of meteoritic addition on airless planetary bodies.

Assessment of water quality and associated human health risk of a tropical freshwater body in Edo State, Nigeria

The quality of freshwater sources is a key factor in sustainable development. This study investigated the water quality suitability of Ossiomo River for human consumption and the implications for public health. Water samples were collected and analysed from October 2021 to March 2022. Results indicated that the water physico-chemical parameters from sampled locations were within their respective National Environmental Standards and Regulation Enforcement Agency (NESRA) permissible limits except for pH (< 6.5), dissolved oxygen (< 6.0mg L−1), cadmium (> 0.005m /L−1), manganese (> 0.05mg L−1) and total hydrocarbon content (>10mg L−1). Comprehensive pollution index (0.4–1.0) and water quality index (251.57–765.37) values indicate that the water body was slightly polluted and unsuitable for human consumption (WQI > 50). Health risk assessment showed that children and adults were predisposed to non-carcinogenic risk (HIoral > 1) and carcinogenic risk (ICR: 1.21E-02 and 2.84E-03) from heavy metals through oral exposure. Natural run-off and anthropogenic activities were identified sources of heavy metals and hydrocarbons within the catchment. The study has provided data for water resource quality monitoring and raised concerns as to the need for immediate action to safeguard the public health of communities surrounding the Ossiomo River, through the provision of alternative sources of potable water.

[Health Risk Assessment of Heavy Metals in Soils of a City in Guangdong Province Based on Source Oriented and Monte Carlo Models].

Taking a city in Guangdong Province as the research area, the concentration and spatial distribution characteristics of heavy metals in the surface soil were studied to clarify the situation of soil heavy metal pollution and priority control factors, providing basic data for the prevention and control of soil heavy metal pollution in the city. The content characteristics of heavy metals in 221 soil samples in the city were analyzed, and the potential health risk assessment and source analysis were carried out through the Monte Carlo model, the potential health risk assessment (HRA) model, and the PMF receptor model. It was found that heavy metals ω(As), ω(Hg), ω(Cd), ω(Pb), ω(Cr), ω(Cu), ω(Ni), and ω(Zn) in the soil of the city were 18.16, 0.43, 1.46, 68.57, 98.34, 64.19, 26.53, and 257.32 mg·kg-1, respectively, with a moderate to high degree of variation. Except for Ni concentration, the soil concentrations of other heavy metal elements exceeded the background values of soil in Guangdong Province to a certain extent, and the concentrations of Cd and Zn exceeded the national secondary standards, resulting in severe heavy metal pollution; the main sources of heavy metals were industrial sources, and natural parent materials, lead battery manufacturing, transportation, artificial cultivation, and pesticide and fertilizer inputs also had an undeniable impact on the accumulation of heavy metals in the soil. Heavy metals in the soil had a certain degree of tolerable carcinogenic health risk for both children and adults, whereas non-carcinogenic risks could be ignored. The potential health risk of children was greater than that of adults, and the main exposure route was through oral intake. The input sources of pesticides and fertilizers and As should be the main controlling factors for the health risks of heavy metals in the city's soil, followed by mixed sources and Cr. There were differences in the spatial distribution characteristics and relative pollution levels of heavy metals, and it is necessary to deepen zoning monitoring and control, strengthen soil pollution prevention and control, and reduce human input of heavy metals in soil.

Influencing Factors, Risk Assessment, and Source Identification of Heavy Metals in Purple Soil in the Eastern Region of Guang’an City, Sichuan Province, China

Soil heavy metal contamination poses a significant threat to both environmental health and ecological safety. To investigate the influencing factors, ecological hazards, and sources analysis of heavy metals in purple soil, 27 sets of soil samples were collected from varying genetic horizons within Guang’an City, and the contents of As, Cd, Cu, Cr, Hg, Ni, Pb, and Zn were analyzed. The results indicated higher concentrations of heavy metals in soil A horizon, compared to that of C horizon. The relevance analysis indicated that the soil’s heavy metals were strongly correlated with the soil’s physicochemical properties. The enrichment factor, pollution load index, and potential risk index highlighted slightly to severely polluted levels of soil Cd and Hg, which significantly contribute to the ecological hazards posed by soil heavy metals. The potential source of heavy metals analyzed using the APCS-MLR model identified both anthropogenic inputs and natural sources as primary contributors to heavy metal presence in soils. The Cu, Cr, Ni, Pb, and Zn contents in the samples from different genetic horizons were chiefly influenced by natural sources, such as soil matrix erosion and weathering, while the concentrations of Cd and Hg were largely affected by anthropogenic activities, specifically coal combustion and agriculture. Conversely, the As content was found to be influenced by a combination of both factors. Anthropogenic activities greatly impacted soil heavy metals at various depths within the study area, thereby underscoring the importance of monitoring these heavy metals. The findings gained from this research can give a scientific basis for the potential utilization of purple soil.

Impact of Heavy Metal Pollution on the Environment

Pollution of the environment by the toxic heavy metals is a global issue of concern and affects the natural quality of the air, water, and soil. Anthropogenic activities are largely responsible for the widespread pollution of heavy metals in the environment, which is having a harmful impact on human health. Rapid urbanization, industrialization, population explosion, and use of advanced technology in developing countries have resulted in huge rise in waste production. Waste generation and disposal along with landfills is a serious global environmental threat resulting in heavy metal contamination of the soils, water, and plants. Heavy metals reaching in the atmosphere result to the deterioration of the quality, and contamination of the soil and groundwater along with damage to the living organisms. The present review describes the analysis of heavy metal pollution of the environment with respect to air, animals, aquatic ecosystem, plants, and soil. Special emphasis is provided on sources of heavy metals in the environment, harmful impacts of heavy metals on the environment and strategies to control heavy metal pollution of the environment. Present study is based on critical review and analysis of scientific information published by academic and professional researchers who studied the impact of heavy metal pollution on the environment. Research articles on impact of heavy metal pollution on the environment published in high impact factor journals were referred for collection of databases. This study notices that there is an urgent need for continuous monitoring of various environmental elements for heavy metals in different open dumpsites. It also recommends that nanomaterials, such as metal oxide nanoparticles, graphene and its derivatives, magnetic nanoparticles, and carbon nanotubes should be used to remove the toxic heavy metals from the air, water and soil.

Differentiating anthropogenic effects from natural metal(loid) levels in residential soil near a zinc smelter in South Korea.

Metal(loid)s pose a significant hazard due to inherent toxicity. Individuals are particularly exposed to metal(loid)s in soil through direct or indirect contact. Identifying metal(loid) sources in soil is required for exposure mitigation to anthropogenic metal(loid)s, while metal(loid)s are natural constitutes of soil. Metal(loid) concentrations and Pb isotopes were determined in residential soil profiles impacted by a Zn smelter to distinguish the anthropogenic effect from natural levels. One hundred sixty-nine core soil samples were collected from depths down to 5.5m below ground level at 19 sites and were divided into Zn-Cd-As- and As-contaminated groups based on the worrisome level (WL) of soil contamination. The Zn-Cd-As-contaminated group (n = 62) was observed at depths < 1m, showed high Zn levels (mean of 1168mg/kg) and Cd and As frequently exceeding WLs, and had low 206Pb/207Pb ratios close to the Zn smelter. In contrast, the As-contaminated group (n = 96) was observed at depths > 1m, did not have other metals exceeding WLs, and showed a wide range of 206Pb/207Pb ratios far away from the Zn smelter. The results indicated that the pollution sources of Zn-Cd-As- and As-contaminated soils were fugitive dust emissions from smelter stacks and geology, respectively. The metal(loid)s in host rock set geochemical baselines in soil profiles, while smelting activities affected the upper layers over 50years. This study demonstrated the effectiveness of utilizing the vertical distribution of metal(loid) concentrations and Pb isotopes in soil profiles for distinguishing between anthropogenic and geogenic origins, in combination with baseline assessment.

Using Hg isotopes and trace elements to constrain the origin of the Ordovician Xiangquan Tl deposit, South China

Sediment-hosted stratiform sulfide (SHSS) deposits commonly contain large amounts of strategic metals, such as Tl, Hg, Cd, Ge and Ga, however, sources of these metals remain debate. Here we present new elemental and Hg isotopic data to constrain the metal sources for the Xiangquan Tl deposit (South China), a unique SHSS deposit with 250 t Tl at an average grade of 928 ppm. Stratiform pyrite orebodies are hosted in the Ordovician marine sedimentary succession of mostly limestone with minor mudstone. Pyrite, the dominant ore mineral, is rich in Hg (up to 1360 ppm). Bulk ores and pyrite separates from this deposit have significant variations of δ202Hg (−5.48 to −0.65 ‰) and Δ199Hg (−0.01 to 0.36 ‰). The Δ199Hg values are mostly positive, similar to those of seawater and marine sediments. Ore petrography, trace element enrichment coefficients, rare earth element patterns, Re-Os ages (478 ± 33 Ma) and S isotope compositions of pyrite indicate that Hg and other metals were derived from hydrothermal fluids venting at the seafloor. We suggest that the ore-forming fluids of the Xiangquan deposit were predominantly originated from large-scale circulation of evolved seawater, which leached Hg and Tl from the marine country rocks. These metal-rich fluids migrated upward, vented to the seafloor, and mixed with anoxic H2S-rich seawater to precipitate Hg- and Tl-rich pyrite. Our study highlights that the combined application of Hg isotopes and trace elements could be used to trace the sources of metals in hydrothermal ore deposits such as SHSS deposits.

Holistic Perilous Index-Based Environmental Appraisal of Metal(oid)s in the Sole Coral-Bearing Island of Northeastern Bay of Bengal

This study aimed to evaluate the concentration, distribution, along with the environmental and human health impact of eight heavy metals—Pb, Cr, Cu, Cd, Zn, Mn, Ni, and As—on St. Martin's Island in the northeastern Bay of Bengal, and in doing so to help implement new legislations to protect the island. Focusing on the island's significance as a tourist destination, with seafood being a prominent dietary component, three sample types (sediment, seawater, and crustaceans) were selected for a comprehensive assessment, considering seasonal variations. Concentration of metals was observed to be lower than the established standards in sediment samples, but in seawater samples, Pb, Cr, Cd and Zn were higher than US-EPA values for natural marine water. The metals displayed a decreasing trend of Zn > Ni >Pb> Cu >Mn> As > Cd > Cr in crustacean samples for both seasons. Crustacean samples displayed higher metal concentrations in winter than in monsoon. Pb exceeded the maximum allowable limit for crustaceans with a concentration of about 3 and 4 mg kg-1 in monsoon and winter respectively; being more than 6-8 times the standard for Bangladesh which is only about 0.5 mg kg-1. Health indices displayed that although adults may suffer less from carcinogenic/non-carcinogenic health effects, the risks are far greater for children. For both age groups, As and Ni displayed possibilities of developing cancer. Principal Component Analysis (PCA)shed light on the sources of metals and showed that most of them were from anthropogenic sources. Overall, this study found that the quality of the environment of the island was better in comparison to previous studies made before the pandemic, and so, if the trend continues, it may lead to a better environment for the organisms around the island and help to keep the negative physiological impacts from the consumption of these organisms to a minimal.

Polyoxometalate Coupled Polymers Induced Molybdenum Phosphide with Large Surface Area for Efficient Hydrogen Evolution

Developing highly active hydrogen evolution reaction (HER) electrocatalysts possesses great significance for the green renewable energy conversion and storage. Here, through the electrostatic attraction between polyoxometalate (PMo12) and ammonium polyphosphate (APP) and the coordination with polyallylamine hydrochloride (PAH), the precursor was constructed, and then nitrogen-doped graphite carbon layer-coated MoP active particles (MoP@NC) were successfully prepared by high temperature carbonization. For HER, the overpotential of η10 for MoP@NC is 119 and 126 mV in acidic and alkaline electrolyte. Furthermore, in alkaline solution, when the current density reaches a certain degree (≥110 mA cm−2), the hydrogen production activity of the catalysts are the same as that of the industrial Pt/C catalysts, or even have a slight advantage. The synergistic interaction of active particles (MoP) and graphitic carbon layers and high specific surface area ensure the excellent activity of HER. N-doped porous carbon layers also protect MoP@NC working for 24 h. Moreover, the catalysts prepared in the same experimental environment with ammonium molybdate as metal source also showed good HER performance in acidic and alkaline environments. This study opens a general way to develop earth-rich Mo-based phosphide electrocatalysts with high activity for hydrolysis applications.

The advances in the recovery process for precious metals from nickel slag, a review

The creation of nickel-smelting products including important metals like nickel, cobalt, and copper is a persistent issue in the nickel mining business. Another secondary source of precious metals is nickel slag. In addition, the massive amounts of nickel slag generated by the nickel smelter sector will pollute the environment, particularly the soil, since the smelting slag contains hazardous materials. This study examines techniques for recovering precious metals from nickel slag by reviewing publications from Springer Link, Google Scholar, MDPI, ScienceDirect, Membrane Journal, and other authors. The two types of metal recovery techniques from nickel slag that were examined were hydrometallurgical and pyrometallurgical techniques. This review article describes a pyrometallurgical method that involves roasting and selective reduction. In the meantime, the hydrometallurgical techniques were examined in the high-pressure oxidative acid leaching process, the atmospheric acid leaching method, and the bioleaching process. A roadmap for research designs that can be used to recover valuable metals from nickel slag sustainably has been created due to the completed literature evaluation.

Comprehensive recycling of slag from the smelting of spent automotive catalysts

Spent automotive catalyst is a valuable source of platinum group metals (PGMs), making them crucial secondary resources. Currently, the main process for recovering PGMs from these catalysts is metal capture method. The smelting process would produce a significant amount of residual slags containing various components like SiO2, Al2O3, CaO, Fe2O3, Na2O, as well as high levels of heavy metals including Cr, Pb, and Ni. These slags are considered either solid waste or hazardous waste and usually disposed of in landfills, which can have detrimental effects on the environment. Furthermore, the smelting slags also contain approximately 2–5 % rare earth elements and trace amounts of precious metal elements. In this study, vacuum carbothermal reduction is employed to pretreat the smelting slags. This method not only successfully removes the heavy metal element lead, but also efficiently achieves the recovery of rare earths, and the enrichment of platinum group metals by mineral phase transformation of cerium-zirconium solid solution and in-situ iron capture. The lead removal rate exceeded 99 %, and the grade of precious metals in the enrichment process was approximately 12 times higher than the original material, with a recovery rate more than 90 %. The leaching rate of rare earths also increased from less than 50 % to more than 95 % after vacuum carbothermal reduction. The effect of vacuum carbothermal reduction pretreatment on the smelting slag phase was systematically studied, and the mechanism behind the increasing rare earth leaching rate due to this pretreatment was further analyzed.

Heavy metals in surface sediments of lake patria wetland, southern Italy, and environmental risk

The study investigated the presence of heavy metals in the surface sediments of one of the most important wetlands in south Italy, Lake Patria, and the related environmental risk. Surface sediments were analyzed for particle size and shape, total organic carbon and As, Cd, Cr, Cu, Fe, Hg, Ni, Pb and Zn levels. Mean total organic carbon was high, 3.1 %, with a peak of 5.9 % near the input of freshwater channel whereas sediments appeared to be mainly composed of sand and/or gravel and significantly polluted by metals especially Cr, Cu and Zn. Data from heavy metals spatial distribution, Pearson correlation, principal component analysis and geochemical indices suggested dominant anthropogenic source for most metals. Mean Igeo values of Cr, Cu and Ni were in the range of 4.6–7.3 of strongly polluted class while their relative mean enrichment factors were largely exceeding the threshold of the anthropic pollution, 1.5. A very high pollution situation was also outlined when considering the Cf indices, with Cr, Cu and Ni possessing mean values from an order of magnitude of ten to hundred times higher the very high polluted class, 6 ≤ Cf. On the overall, the integrated indices of modified contamination degree, pollution load and ecological risk revealed a serious pollution scenario. The mean comprehensive ecological hazard index was fivefold the most critical limit, ≥600, in almost all the lagoon and especially in the locations close to channel.

Klang River Water Quality Assessment and Its Effects on Human Health Using Chemometric Analysis

Introduction: River water pollution has been a significant hazard to human health and is associated with severe health risks. This study evaluates water quality and heavy metal levels in the Klang River, analyzing their health risks through chemometric analysis. Methods: Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) was used to analyse the heavy metal contents in river water samples obtained from 9 sampling stations. Chemometric statistical techniques (principal component analysis (PCA) and hierarchical cluster analysis (HCA)) are employed to identify the sources of physicochemical properties and heavy metals. The human health risk was evaluated using statistical analysis, apart from hazard quotient (HQ), hazard index (HI), and carcinogenic risk (CR). Results and Discussion: Results showed that the physicochemical parameters were within acceptable limits. The concentration of heavy metals was found to follow a decreasing order of As &gt; Ni below permissible levels, except at P9 and P8. PCA and HCA showed important connections among parameters, emphasizing that COD, NH3N, and TDS are key factors affecting Klang River water quality. Conclusion: The study assesses pollution risks in the Klang River, offering crucial insights for sustainable estuary management. It highlights significant changes in temperature, pH, TDS, BOD, DO, and NH3N levels, along with specific trends in heavy metal concentrations. The Health Risk Assessment indicates acceptable HQ and Target Cancer Risk values. However, the study's limited sample sites and focused timeframe might hinder understanding long-term patterns and regional differences. Extended data collection and additional information are necessary to improve water quality management and protect public health

Pollution Characteristics and Risk Assessment of Heavy Metals in the Sediments of the Inflow Rivers of Dianchi Lake, China

To explore the contamination status and identify the source of the heavy metals in the sediments in the major inflow rivers of Dianchi Lake in China, sediment samples were collected and analyzed. Specifically, the distribution, source, water quality, and health risk assessment of the heavy metals were analyzed using correlation analysis (CA), principal component analysis (PCA), the heavy metal contamination factor (Cf), the pollution load index (PLI), and the potential ecological risk index (PERI). Additionally, the chemical fractions were analyzed for mobility characteristics. The results indicate that the average concentration of the heavy metals in the sediment ranked in the descending order of Zn &gt; Cr &gt; Cu &gt; Pb &gt; As &gt; Ni &gt; Cd &gt; Hg, and most of the elements existed in less-mobile forms. The Cfwas in the order of Hg &gt; Zn &gt; Cd &gt; As &gt; Pb &gt; Cr &gt; Ni; the accumulation of Hg, Zn, Cd, and As was obvious. Although the spatial variability of the heavy metal contents was pronounced, the synthetical evaluation index of the PLI and PERI both reached a high pollution level. The PCA and CA results indicate that industrial, transportation, and agricultural emissions were the dominant factors causing heavy metal pollution. These results provide important data for improving water resource management efficiency and heavy metal pollution prevention in Dianchi Lake.

Characterization, Concentration, and Speciation of Metal Elements in Copper Slag: Implications for Secondary Metal Recovery

The treatment of large amounts of copper slag is an unavoidable issue resulting from the high demand for copper during the global transition to a sustainable development path. Metal-rich copper slag might serve as a potential source of metals through secondary recovery. In this study, two copper slags (CS1 and CS2) with different metallurgical properties were characterized, focusing on secondary metal recovery. The X-ray diffraction (XRD) results show that fayalite (Fe2SiO4) and magnetite (Fe3O4) were the main crystalline phases in both CS1 and CS2. In addition, CS2 exhibited a more stable amorphous silicate network than CS1, which was attributed to the differences in the content of Si-O-3NBO linkages. The sequential extraction of Zn, Cu, Fe, and Pb from the slags was also explored, with the Cu content in CS1 being substantially lower than that in CS2. All metals were distributed in the F5 residue fraction. Cu was the most mobile metal as a result of the large proportion of soluble fractions (F1–F3), followed by Zn and Fe. This study explored the chemical speciation of Zn, Cu, Fe, and Pb from copper slags, which has practical implications for secondary metal recovery from such materials.

Iron dissolution from Patagonian dust in the Southern Ocean: under present and future conditions

Although the input of desert dust as a key source of trace metals in the Southern Ocean (SO) has been previously studied, the dissolution process of metals in surface waters, particularly iron (Fe), remain poorly understood. Given the crucial role of Fe in primary production and the biological carbon pump in the SO, we focused on experimental estimations of Fe dissolution from Patagonian dust, the primary natural dust source in the SO. Our study considered both current and projected future conditions, encompassing sea-surface warming, acidification, increased photosynthetically active radiation, and doubled dust inputs. Through controlled laboratory experiments using filtered SO seawater, conducted over 7 days, we assessed changes in particulate Fe (pFe) concentrations, Fe redox speciation (Fe(II)/Fe(III)), and in the mineralogy of Fe-bearing dust in abiotic condition. The predominant minerals in the dust included quartz and aluminosilicates, with silicon (Si), aluminum (Al), and Fe as the major elements. No significant alterations in the mineralogy and the elemental composition of the dust were recorded during the dissolution experiments, neither under present nor under projected future conditions. The particulate Fe(II)/Fe(III) ratio remained consistently at 0.25 during the experiments, unaffected by changed conditions. Consequently, changes in environmental conditions in the SO would therefore not significantly alter the mineralogy and redox speciation of pFe in the Patagonian dust. On the contrary, pFe exhibited a dissolution rate of 3.8% and 1.6% per day under present and future conditions, respectively. The environmental changes anticipated for 2100 in the SO will likely to result in a decrease in the dissolution rate of pFe. Thus, even though a doubling of dust input by 2100 is anticipated, it will unlikely provide significantly more dissolved Fe (dFe) in seawater in the SO. Consequently, the future intensification of Patagonian dust inputs may not alleviate the Fe limitation in the SO.

Concentrations and probable health risks of potentially toxic metals (Pb, Cd and Cr) in some Nigerian lipstick products

BackgroundLipstick is one of the widely used cosmetic items that are produced from both natural and processed materials and they are one of the sources of metals and metalloids released among the users. This study measured concentrations of Pb, Cd and Cr in some brands of Nigerian lipstick products and assessed their probable health risks to the users. MethodsA total of twenty (L1 - L20) brands of lipstick products were purchased from the central cosmetic stores and the samples were prepared, digested and concentrations of Pb, Cd and Cr were determined using Atomic Absorption Spectrometry (AAS). The probable health risk was assessed via average daily dose (ADD) by ingestion route, hazard quotient (HQ), hazard index (HI), cancer risks (CR), and relative intake index (RII). ResultsThe ranges of concentrations of Pb, Cd and Cr were 5.6 - 25.1, 2.5 - 21.5 and 5.0 - 61.7 μg g−1, respectively. The ranges of ADD values of Pb, Cr and Cd were 1.2 × 10−3 - 5.7 × 10−3; 1.3 × 10−3 - 5.7 × 10−3 and 5.1 × 10−3 - 1.4 × 10−3 µg day−1, respectively. Among the samples Cr had HQ values 1.3 to 9.6. The HQ values of Cd for L2, L6, L12 and L14 ranges between 1.1 and 1.5. Then HQ values of Pb for L1 -L20 were 1.0 - 4.1. The HI values of Pb, Cr and Cd in each lipstick brands range from 2.8 to 12.5, indicating a non-carcinogenic health risk. The CR values for Cr and Cd are from 6.6 × 10−4 to 6.9 × 10−4 and from 2.0 × 10−2 to 2.5 × 10−2, respectively and they were within the acceptable limit value of 1.0 × 10−4. The RII of Pb, Cd and Cr were 4.50 - 20.1, 2.0 – 19.2 and 1.9 – 23.0 %, respectively. ConclusionAll the health indices indicated non-carcinogenic health risks. The continuous exposure and unintentional ingestion of such lipstick products can pose high risks to the users due to bioaccumulation of Pb, Cd and Cr which may lead to negative health conditions.

Determination of Heavy Metal Sources in an Agricultural Catchment (Poland) Using the Fingerprinting Method

This study investigates the heavy metal contamination of soils and suspended sediments in the Nurzec River catchment (Eastern Poland), focusing in particular on the effects of catchment land use. The fingerprinting technique has been combined with the classic, Igeo, and EF index-supported contamination analysis to identify heavy metals sources. A wide range of elements (31 chemical elements including heavy metals) allowed the author to analyse the pathways and to identify the pressures of heavy metal contamination. The developed statistical models of heavy metal source distribution displayed results at a statistically significant level. The results have revealed the significant impact of land use connected with urban areas (URBAN) and pastures (PAST), which together constitute less than 20% of the river catchment area. These results are relevant to the local authorities and stakeholders, as they highlight the significant impact of low-density urban areas that are not locally considered as the major sources of heavy metal pollution. These results will contribute to sustainable decisions in the field of contaminated catchment area remediation.

Metal-for-Amber in the European Bronze Age

Abstract Baltic amber is often considered the principal Scandinavian commodity exchanged for metal from ore-rich regions in Europe. If correct, this may explain the astonishing metal wealth of the Nordic Bronze Age and the modest social consumption of amber locally. The hypothesis of a metal-for-amber principle behind the trade is here for the first time assessed on scales from micro to macro. Amber finds were charted across Europe, and the result was then compared to evidence for regular shifts in copper ore preferences/availability, as found in the systematically changing isotopic/elemental composition of Nordic metal objects in c. 2100–1200 BC. Comparisons indicate that amber and metal followed similar spatiotemporal trajectories with major reorganizations at the turn from the Early to the Middle Bronze Age. Shifts in amber distribution correlate with the geography of metal sources used in both periods and flows of metal to Scandinavia and amber to Europe appear to be contingent even in subperiods. Major European amber tracks – and the crossroads hubs controlling them – were identified for the transfer of goods, yet again revealing major changes at the transition to the Middle Bronze Age. The social roles and meanings of amber among Nordic communities were likewise examined, suggesting that bearers of amber played a role in exercising social control of this resource. It is concluded that amber almost certainly was exchanged for metal.