Source Of Cr Research Articles

Characteristics, Health Risks, and Source Analysis of Heavy Metal Pollution in Surface Soil in Shanxian County

Soil heavy metal （HM） pollution is a prominent global environmental problem. Understanding the risk characteristics and quantitative analysis of potential sources of soil HM pollution is of great significance for accurate prevention and control, scientific management, and safe utilization of soil resources. In the surface soil of Shanxian County, the contents of eight HMs, such as As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn, were collected and identified in 330 surface soil samples. The HM pollution degree was evaluated using the accumulation index and enrichment index. The carcinogenic and non-carcinogenic risks of HMs were evaluated using the health risk model designated by the Ministry of Ecology and Environment. The sources of HMs in topsoil were analyzed using correlation analysis, principal component analysis, cluster analysis, absolute principal component score-multiple linear regression （APCS-MLR）, and other qualitative and quantitative methods. The results showed that all eight HM elements in the surface soil samples were lower than the background values and the screening values of agricultural land soil pollution risk in Heze City. According to Igeo and EF evaluation, only approximately 5% of Hg samples were slightly polluted, and the other seven HMs were non-polluted or slightly polluted. The carcinogenic risk and non-carcinogenic risk of As for adults and children in surface soil were at tolerable levels, and the carcinogenic risk and non-carcinogenic risk of the other seven HMs for adults and children could be ignored. The main sources of Cd, Cu, Zn, Ni, and As in the surface soil were natural background sources； the main sources of Cr and Hg were agricultural breeding sources and industrial coal sources, respectively； and the main pollution sources of Pb included other unknown sources and natural background sources. The average contribution rates of natural background sources, agricultural breeding sources, industrial coal sources, and other unknown sources were 51.69%, 27.18%, 6.83%, and 14.31%, respectively, indicating that the main sources of heavy metals in the surface soil of Shanxian County were natural background sources, followed by agricultural breeding sources.

Occurrence and enrichment mechanisms of groundwater hexavalent chromium in typical loess area of China.

Understanding the geochemical mechanisms governing hexavalent chromium (Cr(VI)) in groundwater is essential for mitigating health risks. However, the processes driving Cr(VI) accumulation and migration in loess regions remain insufficiently understood. This study investigated the occurrence, release, and migration mechanisms of Cr(VI) across different groundwater environmental units (GEUs) in the south-central Loess Plateau, China. This study used combined approach of isotopic analysis, multivariate statistical methods, hydrochemical graphical methods, and GIS technology to reveal the origins and processes influencing Cr(VI) hydrogeochemistry within these GEUs. The results revealed significant spatial variability in Cr(VI) concentrations among the GEUs, ranging from below the detection limit to 300μg/L, with nearly 40% of samples exceeding the WHO limit. Pronounced enrichment of Cr(VI) was observed in the fissure-pore water of the loess tableland and pore water of the alluvial plain. Cr(VI) enrichment and release in the GEUs were facilitated by oxidative conditions (high Eh, SO42-/HCO3-, Mn-oxide presence) and cation exchange processes under slightly alkaline conditions (pH>7.80). Key hydrogeological processes and geomorphological factors, including lateral runoff recharge, slow groundwater flow in the loess tableland, vertical recharge, extensive water-rock interactions, and hydraulic gradients were identified as critical divers of Cr(VI) migration and enrichment across different GEUs. Under reductive conditions, Cr(VI) was reduced to Cr(III), particularly in the pore water of the alluvial plain, but competitive adsorption with nitrate allows the enrichment of Cr(VI) in groundwater, particularly in the fissure-pore aquifer. A conceptual model was developed to elucidate Cr(VI) sources and migration mechanisms in groundwater, offering a framework for risk mitigation and management of groundwater in loess regions.

Heavy metal contamination of vegetables in China: status, causes, and impacts.

Exposure to heavy metals from vegetable consumption poses a serious health risk to the Chinese population. The lack of knowledge on the overall status of vegetable contamination at the national level hinders the development of national regulations on preventing heavy metal exposure. To address this issue, the study presents an overview of heavy metal contamination in vegetables across China based on 96 peer-reviewed studies published over the past 20years. The average concentrations of As, Cd, Cr, Cu, Mn, Ni, Pb, and Zn in the edible parts of vegetables are 3.7 ± 12.9, 1.6 ± 4.0, 4.3 ± 10.3, 18.6 ± 27.6, 164 ± 281, 4.5 ± 5.5, 7.7 ± 23.7, and 105 ± 283mgkg-1 (dry weight), respectively. The associated daily exposures are 0.1-5.7, 0.1-1.7, 0.6-4.2, 4.1-20.5, 26-107, 0.7-3.0, 0.4-16.0, and 13-93μgkg-1 d-1, respectively. General linear models explained 80%, 44%, 83%, 79%, 64%, 81%, 65%, and 55% of the total variance in As, Cd, Cr, Cu, Mn, Ni, Pb, and Zn concentrations in vegetables, respectively, based on vegetable type and selected geological, meteorological, economic, and environmental factors. Agroforestry is the main source of heavy metal contamination, accounting for 3%-30% of the total variance in heavy metal concentrations in vegetables. Mining, smelting, refining, metalworking, and electrical equipment manufacturing are important source of As, Cr, Cu, Mn,Ni, and Pb, accounting for 7%-17% of the total variance.

A novel layered culture device reveals spatial dynamics of root element uptake and optimal silicon application site for mitigating chromium uptake by rice

Understanding root uptake mechanisms for various elements is crucial for optimizing heavy metal remediation strategies and enhancing plant-nutrient interactions. However, simple and effective methods to differentiate the contributions of specific root segments in element uptake are lacking. Here, we developed a layered culture device consisting of a culture box and a plant suspension mechanism, which isolates different root segments through solid media and waterproof coating. Then, we used the device to investigate the roles of distinct root segments (0–1 cm and 1–2 cm from the tip) in heavy metal chromium (Cr) and beneficial element silicon (Si) uptake in rice. The results indicated that the 0–1 cm root segment contributed approximately 58% of leaf Cr(VI), with higher efflux compared to the 1–2 cm segment. Conversely, the 1–2 cm root segment served as the primary source of leaf Si and Cr(III), accounting for 62% and 54%, respectively. The translocation factors for Cr(VI) were similar for both segments (0.039 and 0.032), while the Cr(III) translocation factor for the 0–1 cm root segment (0.061) was 2.8 times that of the 1–2 cm segment. Notably, Si application to the 0–1 cm segment most effectively alleviated Cr (III) and Cr (VI) stress, boosting shoot length, fresh weight, and chlorophyll concentration and reducing Cr concentrations in roots and leaves by 24.7%–65.7%. In contrast, Si application to the 1–2 cm segment had minimal impact on rice growth or Cr uptake. These results suggest a deep Si application strategy for remediating Cr-contaminated soil. The innovative device provides a scientific foundation for distinguishing element uptake contributions of different root segments and enhancing the utilization efficiency of remediation materials and nutrient management in agriculture.

Pollution and Ecological Risk Assessment of Potentially Toxic Elements in Sediments Along the Fluvial-to-Marine Transition Zone of the Don River

The quality of sediments in the mixing zone of river freshwater and marine saline water as an important geochemical barrier for potentially toxic elements (PTEs) remains poorly understood. This study aims to analyze the current pollution with PTEs and associated ecological risks in sediments of the Don River delta and the surrounding area of the Taganrog Bay of the Sea of Azov (Russia). The PTE content was determined in fifty-four collected samples using the WDXRF and assessed using geochemical and ecotoxicological indicators. The source of Cr, Mn, Ni and Pb is mainly river runoff, and Cu, Zn and Cd are from a variety of anthropogenic sources. As shown by the assessment of the geoaccumulation index (Igeo), single pollution index (PI) and contamination factor (CF), these elements are the priority pollutants. According to these estimates, high and very high contamination of sediments in the estuarine zone of the Don River with Cd and Pb was detected in 72–94% and 2–57% of samples, respectively. However, environmental risks are determined almost exclusively by the level of Cd. Total contamination as assessed by the Nemerow pollution index (NPI), modified degree of contamination (mCd) and metal pollution index (MPI) is of concern in 83–98% of the samples studied. The most heavily polluted sediments are in the vicinity of residential areas of the Taganrog Bay. Despite the lower average pollution levels of deltaic sediments, freshwater biota are exposed to higher potential toxic risks of adverse effects by PTE, particularly from Ni and Pb. Thus, the complex hydrological regime and uneven anthropogenic impact predetermine the geochemical state of the sediments of the estuarine zone of the Don River.

In-situ reaction-generation self-healing superior antioxidation layer induced by Al-Y sol-gel film on the AISI304 steel

In this study, an Al-Y sol-gel film is prepared on the AISI304 steel and its effect on the high temperature oxidation resistance is evaluated by the cycle oxidation at 900 ℃ in the air. The resulting intact oxide layer, composed of (Al, Cr)2O3 and MnCr2O4 phases, effectively slowing down the oxidation rates at 900 ℃. The general cracks in the sol-gel film during the oxidation process are found to be self-healed by a growing spinel MnCr2O4 phase from the substrate, attributed to its low Gibbs free energy and the sufficient Cr source from the adjacent substrate. Furthermore, the oxide layer originates from the interaction between sol-gel film and the substrate which enhances the binding between the oxide layer and the substrate. Thus, it could be confirmed that a self-healing superior antioxidation layer is generated on the surface of AISI304 steel through an in-situ reaction induced by the Al-Y sol-gel film during high-temperature oxidation procedure.

Pollution Characteristics, Risk Assessment, and Source Analysis of Heavy Metals in Soil from a Typical Abandoned Antimony Smelting Factory

Considering the surface soil （0-20 cm） from a typical abandoned antimony smelting factory area in Dachang Town, Qinglong County, Guizhou Province, as a case study, a total of 14 soil samples were systematically collected from both within and outside the smelting factory area. The analysis focused on the pollution status, distribution characteristics, and potential ecological risks of heavy metals such as Sb, As, Cd, Cr, Pb, Cu, Zn, Ni, and V in the soil. Additionally, an evaluation and analysis of pollution sources were conducted. The results showed that the mean concentrations of heavy metals including ω（Sb）, ω（As）, ω（Cd）, ω（Cr）, ω（Pb）, ω（Cu）, ω（Zn）, ω（Ni）, and ω（V） in the surface soil of the abandoned antimony smelting factory ranged from 4.58 to 15 049.33 mg·kg-1. With the exception of Cr and Ni, all values exceeded the background values of soils in Guizhou province. The single factor pollution indices of Sb and As were 83.61 and 7.01, respectively, indicating severe contamination. In contrast, Pb fell within the non-polluted to slightly polluted range. The comprehensive potential ecological risk of soil heavy metals was characterized by severe potential ecological risk levels for Sb, As, and Cd, while the remaining heavy metals fell within a range of moderate to substantial potential ecological risk levels. The assessment of the geoaccumulation index revealed that the soil in the study area was primarily contaminated by Sb and As, predominantly exhibiting contamination levels ranging from moderate to severe. The results from the RAC method suggested that Sb was the dominant focus for remediation in this abandoned smelting factory. The two primary pollutants, Sb and As, exhibited elevated levels in leachate toxicity, acid-soluble fraction, available fraction, gastric phase, and intestinal phase in terms of bioavailable content, indicating a certain potential hazard. Further, correlation analysis indicated a certain correlation between the total amount of heavy metals and leachate toxicity, available fraction, acid-soluble fraction, reducible fraction, oxidizable fraction, gastric phase extractable fraction, and intestinal phase extractable fraction. The APCS-MLR model indicated that the sources of Sb, As, Zn, Cu, and Cd were primarily industrial, while the sources of Cr and V were mainly natural, and Pb originated mainly from mixed sources.

A framework integrating affinity propagation algorithm and spatial bivariate analysis for enhanced identification and localisation of soil heavy metals pollution sources.

The accurate identification of pollutant sources and their spatial distribution is crucial for mitigating soil heavy metals (SHMs) pollution. However, the receptor model struggles to effectively categorize pollutant sources and pinpoint their locations and dispersion trends. We propose a novel comprehensive framework that combines a receptor model, random forest (RF), affinity propagation (AP) algorithm, and bivariate local indicator of spatial association (BLISA), to optimize the traditional approach for tracing SHMs sources in industrial regions. We apportioned SHMs sources using a receptor model combined with RF, while BLISA combined with AP methods were employed to accurately locate the source areas and identify their dispersion tendencies. The results revealed that SHMs originated from mixed sources of equipment manufacturing agglomeration and agricultural activities (59.0%), geological background (30.5%), and emissions from heavily-polluting industries (10.5%). The pollution sources of soil Cd and Pb were located near specific industries, showing characteristics of multi-site concurrent pollution diffusion influenced by their proximity to industrial sites. The spatial distribution of Cr, Cu, and Zn sources was concentrated in high-density urban industrial areas, transitioning from point to nonpoint sources, with diffusion patterns influenced by the spatial agglomeration effect of industries. Our enhanced framework accurately identifies the location of SHMs sources and their dispersion tendencies, thereby improving regional soil pollution management.

Content, Sources, and Ecological Risk Assessment of Heavy Metals in Soil of Typical Karst County

Soil heavy metals in karst areas have obvious high background value characteristics. Conducting county-level soil heavy metal ecological risk assessment and identifying heavy metal sources in karst areas are of great significance for soil pollution control and land resource management. Taking Pingguo City, a typical karst county in Guangxi Province, as the study object, 3 151 surface and deep soil samples were collected using the grid method and combined to form 785 analytical samples. The contents of eight heavy metal elements, including As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn, were determined. The content characteristics and sources of heavy metals were analyzed using statistical analysis, interpolation analysis, factor analysis, and the absolute principal component-multiple linear regression model （APCS-MLR）. Using the content of heavy metal elements in deep soil （150-200 cm） as background values, the ecological risk assessment of heavy metals in surface soil （0-20 cm） in the study area was conducted using the geo-accumulation index （Igeo） and potential ecological risk index （RI） methods. The results showed that the average content of heavy metal elements in the deep soil of the study area was significantly higher than the background value of the C layer soil in Guangxi Province, and the average content of heavy metal elements in the surface soil was significantly higher than the background value of the A layer soil in Guangxi Province. The spatial distribution of soil heavy metal element content generally showed the characteristics of high in karst areas and low in non-karst areas. The main sources of As, Cr, Ni, Pb, and Zn were soil parent materials, with contribution rates of 74.36%, 84.59%, 93.69%, 79.67%, and 78.17%, respectively. The main sources of Cd were soil parent material sources and unknown sources, with contribution rates of 37.33% and 31.05%, respectively. The main sources of Cu were soil parent materials and unknown sources, with contribution rates of 59.07% and 40.23%, respectively. The main sources of Hg were tectonic activity and mineralization, as well as unknown sources, with contribution rates of 52.49% and 30.65%, respectively. The geo-accumulation index （Igeo） showed that the surface soil was mainly polluted by Cd, with mild or above pollution accounting for 47.78%. The potential ecological risk index （RI） showed that the proportion of surface soil heavy metal comprehensive potential ecological hazards with mild, moderate, strong, and very strong levels was 80.78%, 14.97%, 2.51%, and 1.64%, respectively.

(Digital Presentation) Reactive Evaporation of Cr Vapors from Chromia-Alkaline Oxide Mixtures Generated in 800℃ Air and Subsequent Condensation Onto Aluminosilicate Fibers

This research aims to improve fundamental understanding of the reactive evaporation and condensation of Chromium (Cr) vapors, which are generated from Cr containing alloys used in many high-temperature (>500℃) process environments and can form potentially problematic condensed hexavalent (Cr(VI)) species downstream. This study focuses on the effects of alkaline oxides present in the Cr source on the resultant Cr evaporation and condensation. Vapor species were generated by flowing high-temperature (800℃) air containing 3% water vapor over chromia (Cr2O3) and mixtures of chromia with calcium oxide (CaO) or magnesium oxide (MgO) powders. Lab-grade quartz and alumina fiber samples were positioned downstream from the Cr-alkaline oxide source where the temperature decreases (<500℃) to collect condensed vapor species. Total condensed Cr and ratios of oxidation states were measured using inductively coupled plasma optical emission spectroscopy (ICP-OES) and diphenyl carbazide (DPC) colorimetric/direct UV-VIS spectrophotometric analyses. Preliminary results indicate a decrease in partial pressures of generated Cr vapor species as well as a decrease in condensed Cr species on the aluminosilicate fibers when alkaline oxides are present in the Cr source compared to a pure Cr source. These results also indicate presence of hexavalent Cr (Cr(VI)) species condensed on all samples investigated. Computational thermodynamic equilibrium modelling corroborated the experimental results showing partial pressures of produced vapor species in the presence of alkaline oxides as well as stabilities of condensed Cr compounds on the fiber samples. Comparative results and analyses are presented and discussed to help inform mechanistic understanding and future related research and engineering efforts. Figure 1

Characterization and Source Analysis of Heavy Metal(loid)s Pollution in Soil of an Industrial Park in Kunming, China

This study investigated the characteristics and sources of heavy metal(loid) pollution in the soil of a key industrial park in Kunming, China. In total, 60 soil samples (40 from agricultural land and 20 from construction land) were collected from and around the park. The soil pH and contents of Arsenic (As), lead (Pb), copper (Cu), zinc (Zn), cadmium (Cd), mercury (Hg), nickel (Ni), and chromium (Cr) were measured. The contents of the eight heavy metal(loid)s were analyzed using the background values of heavy metal(loid)s in the Kunming soil. The pollution load, geoaccumulation, and Nemero Comprehensive Pollution Indices were used for environmental risk evaluation. Cluster and principal component analyses were used to resolve heavy metal(loid) sources. Cd was enriched in construction and agricultural soils. As, Hg, Cd, Pb, Cu, and Zn exhibited large spatial differentiation and were significantly affected by the external environment. A regional pollution load index of 3.02 indicated overall heavy pollution. The pollution load index for each heavy metal(loid) indicated light pollution. The geoaccumulation index indicated relatively severe As, Cd, Cu, Pb, and Zn pollution. The Nemero Composite Pollution Index value showed that the study area was heavily polluted, with construction land being mildly polluted by Cd, and agricultural land being moderately polluted. The results of the spatial distribution show that there were high levels of contamination in the center. Correlation and principal component analyses showed that the pollution sources of the eight heavy metal(loid)s varied. Hg, Cd, and Pb originate primarily from industrial and agricultural pollution. Traffic sources significantly impacted Cu, Pb, Cd, and Cr. Natural sources are the main sources of Cr, Ni, and Cd. Ni is also affected by industrial sources, whereas Zn and Cu are affected by agricultural pollution. The influences of As, Cd, and Pb on the surface soil in the study area were more serious. Cd is more widely polluted and should be a priority in controlling soil heavy metal(loid)s.

Contamination Characteristics and Source Apportionment of Heavy Metal in the Topsoil of a Small Watershed in South Taihang

With the rapid development of industrialization and urbanization, the issue of soil environmental pollution is becoming more and more prominent, especially concerning heavy metal contamination, which has garnered significant scholarly attention. The surface watershed formed by waterline is influenced by various factors such as topography, industrial emissions, and agricultural runoff, resulting in a complex process of migration and accumulation of heavy metal elements from multiple sources. In this study, the pollution characteristics and sources of heavy metal elements Hg, As, Pb, Ni, Cd, Cr, Cu and Zn in 165 surface soil samples from the Manghe River watershed in Jiyuan City were comprehensively analyzed using a variety of methods, including statistics, geostatistics, enriched factor analysis and the Positive Matrix Factorization Model (PMF). The results showed that the concentrations of Hg, Cd, As, Cu, Pb and Zn exceeded their corresponding background values with varying degrees of enrichment. Notably, the average contents of Cd, Hg and Pb were 26.70 times, 3.69 times and 4.49 times higher than those in Chinese soils on average, respectively, showing obvious enrichment characteristics. Moreover, there were distinct spatial distribution patterns for each heavy metal element; Ni and Cr exhibited similar trends mainly controlled by the parent material, while human activities significantly affect the other six elements forming high-value areas around mining and related industries. It is noteworthy that Cu, Hg and Zn were influenced by dominant wind direction in autumn and winter, forming sub-high-value zones in southern forested areas; meanwhile, Cu and Zn were also influenced by agricultural fertilizer application as well as surface runoff, leading to secondary high-value areas in the dryland areas. Further analysis revealed a significant positive correlation among these heavy metal elements, suggesting that they may share common sources. Through the PMF Model, four main factors were identified, with factor 2 (36.25%), factor 1 (23.00%), factor 3 (21.20%) and factor 4 (19.55%) ranked in descending order of contribution rate. The heavy metal pollution in the study area was attributed to anthropogenic activities and natural factors, accounting for 63.75% and 36.25%, respectively. Coal mining, chemical industry smelting, vehicle emissions and excessive use of agrochemicals were identified as the main sources of heavy metal pollution. These pollutants entered the soil through direct emissions, atmospheric deposition, transportation and agricultural activities, exerting a significant impact on the soil environment. Therefore, delving into the spatial distribution pattern of soil heavy metal pollution and precise analysis of its sources are of great importance for effective treatment and remediation of soil heavy metal pollution in small watersheds, maintaining healthy soil ecology and safeguarding human health.

Control of paleoclimate and paleoweathering on chromium contents in a non-ultramafic aquifer hosting high chromium groundwater.

Cr(VI) is a carcinogen with proven mutagenic and genotoxic effects. The effects of the depositional environment (e.g., paleoweathering, paleoclimate, and paleoredox condition) on Crenrichment in non-ultramafic aquifer solids are unclear. In this study, we presented the sedimentary characteristics of a borehole from a typical non-ultramafic aquifer with high Cr groundwater in Jingbian, central Ordos Basin, China. Chromium was enriched in the K1h sandstone aquifer, especially at depths of 400-500m, with the highest value of mass transport coefficient (τAl,Cr) up to 92.13% and τAl,Fe up to 33.5%. The provenance of aquifer Cr was predominantly intermediate and felsic igneous rocks with a mafic rock mixture. This mafic source was inferred from Cr-rich granodiorite and mafic/ultramafic rocks in the Yinshan (Daqingshan-Wulashan) Block, northern Ordos Basin. The Cr-rich aquifer in K1h was developed due to a moderate chemical index of alteration (CIA) (mean, 56.7) under relatively warm and humid paleoclimate, as evidenced by high CIA-temperature (CIA-Temp) (mean, 6.79°C) and paleoclimatic index values (mean, 0.40). Fe-Mn redox cycling in the oxic to suboxic environments contributed to aquifer Cr accumulation. Using path analysis, we identified that paleoclimate created favorable weathering conditions and enrichment of Fe contributed to the formation of high-Cr aquifers. The study reveals the formation of positive Cr anomalies in non-ultramafic aquifers, which is the potential source of groundwater Cr, and highlights the effects of depositional factors on Cr accumulation during aquifer deposition or early diagenesis. It can provide new insights into the natural processes of high-Cr sediments occurring in non-ultramafic aquifers.

Distribution and Comprehensive Risk Evaluation of Cr, Cd, Fe, Zn, and Pb from Al Lith Coastal Seawater, Saudi Arabia

Seawater contamination is a global challenge due to its hazardous effects on marine organisms and human health. Twenty-three surface seawater samples were collected from the Al Lith intertidal area along the Saudi Red Sea coast to evaluate the ecological risks and document the potential sources of Cr, Cd, Fe, Zn, and Pb. Contamination factor (CF), contamination degree (Cd), water quality index (WQI), and heavy metal pollution index (HPI), as well as multivariate tools were applied. The average concentrations of HMs (μg/L) had the following order: Zn (6.616) &gt; Pb (0.284) &gt; Cd and Cr (0.268) &gt; Fe (0.197). CF results showed moderate contamination of seawater with Cd and low contamination of Cr, Fe, Zn, and Pb. However, 26.09% of the samples showed considerable contamination with Cd. Average Cd values revealed low contamination with HMs, while 17.39% of the samples showed moderate contamination. HPI average values indicated medium pollution of Al Lith seawater, while 13 samples reported high pollution. The higher HPI values were reported in samples characterized by higher concentrations of HMs, particularly Cd and Zn. Correlation matrix and principal component analysis suggested anthropogenic sources for Pb and Zn, mostly from industrial and agricultural effluents, landfilling, and domestic wastewater, apart from their natural sources.

Distribution, Source, and Contamination of Heavy Metals in Coastal Sediments of Jeddah, Red Sea, Saudi Arabia.

The study investigates heavy metal (HM) contamination in coastal sediments of Jeddah along Red Sea coast, analyzing spatial distribution and sources. 24 samples underwent (ICP-AES) for Fe, Al, Mn, Ni, Pb, Zn, Cu, Cr, Co, Sr, V, and As. HM averages followed Fe ˃ Al ˃ Sr ˃ Mn ˃ Zn ˃ V ˃ Cu ˃ Ni ˃ Cr ˃ As ˃ Co ˃ Pb. Contamination indices revealed severe Sr enrichment, minor As and Co enrichment, and no enrichment for other HMs. Sediment quality guidelines suggest Ni, Cu, Zn, and As risks to benthic communities at some sites, while Cr and Pb pose minimal risk. Multivariate analysis indicates natural sources for Fe, Al, Mn, Ni, Zn, Cu, Cr, Co, and V, and anthropogenic sources for Sr, As, and Pb, linked to agriculture, industry, and urbanization. Increased Sr values may stem from seawater acidification impacting calcitic corals and molluscs.

Grinding siderite with ferric sulfate to generate an active ferrous source for Cr(VI) reduction

Activated siderite, endowed with excellent properties, was simply prepared by co-grinding with Fe sulfate to enhance its high reducing ability for Cr(VI). Batch experiments were conducted to investigate the main affecting parameters, such as material ratio, pH, temperature, etc. The removal of Cr(VI) by activated siderite was completed within 4 h of the reaction. The activated siderite maintained a high removal effect of Cr(VI) within a wide pH range (3–9). Various analytical methods, including XRD, SEM/EDS, XPS, etc., were employed to characterize the samples and discover variations before and after the reaction. The Fe (Ⅱ) in activated siderite becomes highly active, and it can even be released from the solid phase in the mildly acidic liquid phase to efficiently reduce Cr(VI) and mitigate its toxicity. These findings introduce an innovative approach for activating various minerals widely distributed in nature to promote the recovery of the ecological system.

Concentration, Pollution Level, and Sources of Heavy Metals from Household Dust in Ramadi City, Iraq

Researchers and environmental managers have been interested in household dust pollution because exposure to heavy metals has a detrimental effect on health. This study aims to determine heavy metals concentrations (Cd, Cr, Cu, Ni, Pb and Zn), pollution level, and their potential sources in the household dust of Ramadi City, Iraq. The dust was collected from 35 houses. The atomic absorption spectrophotometry method was used to measure concentrations of heavy metals in the dust. The following was the order of the heavy metal mean concentration: Zn &gt; Ni &gt; Cu &gt; Pb &gt; Cr &gt; Cd. These metals’ mean concentrations are below background guidelines. The descending order of the EF values for the measured metals is as follows: Ni (6.35) &gt; Cu (5.40) &gt; Pb (1.53 &gt; Cr (1.24) &gt; Zn (1.14) &gt; Cd (0.84). Results of the calculation of CF for metals measured in house dust in Ramadi City showed values of less than 1 (CF &lt; 1 indicating a minimum contamination level. Based on the results of multivariate statistics (correlation matrix, cluster and principle components analysis), sources of Cr, Cu, Ni and Zn are indoor anthropogenic sources while the sources of Cd and Pb are outdoor anthropogenic.

Suitable conditions and reduction mechanisms of Cr(VI) contaminated groundwater by in-situ bioremediation with molasses

Molasses is an inexpensive and efficient biological carbon source for Cr(VI) remediation. This study explored the application of molasses in the remediation of contaminated aquifers. Under the conditions of 10–30 °C and pH > 6, molasses was effective for the bioremediation of 50 mg L−1 Cr(VI). Under these conditions, Cr(VI) had a faster remediation rate, and the generated Cr(III) had a lower migration risk. The average removal rate of Cr(VI) doubled when the temperature increased from 10 °C to 20 °C. Considering the remediation efficiency of Cr(VI) and total chromium in groundwater, a concentration limit of injected molasses (<5 g L−1) was proposed. When the molasses concentration exceeded 5 g L−1, >40 % of Cr(III) existed in the form of a complex colloid in the solution, which hindered the precipitation removal of Cr(III). Reduction of Cr(VI) by indigenous microorganisms mainly occurs extracellularly. The results of the simulated tank study showed that molasses can rapidly create in-situ biological reaction zones in the aquifer. Molasses migrated faster in deep aquifers thereby enabling a quicker removal of Cr(VI). In addition, it also has a good removal effect on NO3−. This study is of great significance for the application of molasses to reduce Cr(VI).

Comprehensive analysis of metal(loid)s and associated metal(loid) resistance genes in atmospheric particulate matter

Despite global concerns about metal(loid)s in atmospheric particulate matter (PM), the presence of metal(loid) resistance genes (MRGs) in PM remains unknown. Therefore, we conducted a comprehensive investigation of the metal(loid)s and associated MRGs in PMs in two seasons (summer and winter) in Xiamen, China. According to the geoaccumulation index (Igeo), most metal(loid)s, except for V and Mn, exhibited enrichment in PM, suggesting potential anthropogenic sources. By employing Positive Matrix Factorization (PMF) model, utilizing a dataset encompassing both total and bioaccessible metal(loid)s, along with backward trajectory simulations, traffic emissions were determined to be the primary potential contributor of metal(loid)s in summer, whereas coal combustion was observed to have a dominant contribution in winter. The major contributor to the carcinogenic risk of metal(loid)s in both summer and winter was predominantly attributed to coal combustion, which serves as the main source of bioaccessible Cr. Bacterial communities within PMs showed lower diversity and network complexity in summer than in winter, with Pseudomonadales being the dominant order. Abundant MRGs, including the As(III) S-adenosylmethionine methyltransferase gene (arsM), Cu(I)-translocating P-type ATPase gene (copA), Zn(II)/Cd(II)/Pb(II)-translocating P-type ATPase gene (zntA), and Zn(II)-translocating P-type ATPase gene (ziaA), were detected within the PMs. Seasonal variations were observed for the metal(loid) concentration, bacterial community structure, and MRG abundance. The bacterial community composition and MRG abundance within PMs were primarily influenced by temperature, rather than metal(loid)s. This research offers novel perspectives on the occurrence of metal(loid)s and MRGs in PMs, thereby contributing to the control of air pollution.

Moss as a passive biomonitoring tool for the atmospheric deposition and spatial distribution pattern of toxic metals in an industrial city.

Anthropogenic pollution impacts human and environmental health, climate change, and air quality. Karabük, an industrial area from the Black Sea Region in northern Türkiye, is vulnerable to environmental pollution, particularly soil and air. In this research on methodological aspects, we analyzed the concentrations of six potential toxic metals in the atmospheric deposition of the city using the passive method of moss biomonitoring. The ground-growing terrestrial moss, Hypnum cupressiforme Hedw., was collected during the dry season of August 2023 at 20 urban points. The concentrations of Cr, Cu, Cd, Ni, Pb, and Co were determined in mosses by the ICP-MS method. Descriptive statistical analysis was employed to evaluate the status and variance in the spatial distribution of the studied metals, and multivariate analysis, Pearson correlation, and cluster analysis were used to investigate the associations of elements and discuss the most probable sources of these elements in the study area. Cd and Co showed positive and significant inter-element correlations (r > 0.938), representing an anthropogenic association mostly present in the air particles emitted from several metal plants. The results showed substantial impacts from local industry, manufactured activity, and soil dust emissions. Steel and iron smelter plants and cement factories are the biggest emitters of trace metals in the Karabük area and the primary sources of Cr, Cd, Ni, and Co deposition.