Search Results (2,247)

The increasing accumulation of microplastics (MPs) in soils necessitates a better understanding of their effects on soil chemistry and trace element behavior. This study examined the influence of three MPs—low-density poly(ethylene) (LDPE), polypropylene (PP), and poly(ethylene terephthalate) (PET)—on cadmium (Cd) and copper (Cu) mobility in four clayey–sandy soils with similar organic matter content but differing pH, representing acidic and alkaline terrestrial matrices. Soils were incubated with 1% (w/w) MPs at 60% water-holding capacity for 30 and 90 days. Total Cd and Cu concentrations remained largely unaffected; however, time-dependent changes in metal availability and distribution were observed. Extractability (CaCl₂ and DTPA), sequential BCR fractionation, and environmental risk indices (CF, Igeo, RAC, MF, and PLI) indicated slight increases in Cd availability after 30 days, which became more pronounced after 90 days, particularly in acidic soils (pH 5.5). The magnitude of the MP effect followed the trend PET > PP > LDPE in all cases. Among the two target metals, Cd exhibited substantially higher mobility than Cu, as reflected by RAC and MF values. Specifically, Cd RAC (6–35%) and Cd MF (28–63%) values were considerably higher than those of Cu (1.1–3.8% and 15–28%, respectively). Overall, although the general pollution indices remained relatively stable, MPs altered the extractability and geochemical partitioning of the examined heavy metals—particularly Cd—indicating their potential role as vectors in soil environments. These results demonstrate that incubation time, polymer type, and soil pH jointly regulate MP-induced change in Cd and Cu mobility, with important implications for soil ecosystem risk. Full article

Background/Objectives: Mass spectrometry-based multi-attribute methods (MAM) have the potential to transform therapeutic protein analysis by enabling comprehensive monitoring of multiple quality attributes in a single assay. However, the widespread adoption of MAM is hindered by significant challenges, most notably artificial oxidation during sample preparation and analysis. This report summarizes long-term operational observations and several case studies that substantiate this concern. Methods: A tryptic digest, high-resolution LC-MS MAM workflow was applied to an Fc-fusion protein and multiple antibody-based therapeutics, with a frozen reference standard analyzed in each run for system suitability and longitudinal trending. Oxidation excursions were investigated by comparing laboratories, consumables, LC-MS configurations, and other method parameters. Results: In a seven-year trending record, apparent total methionine oxidation in the Fc-fusion protein reference standard showed an abrupt, sustained increase (up to ~5-fold); the shift was traced to a specific bag of microcentrifuge-tubes used during buffer exchange and resolved after those tubes were discontinued. In an antibody–drug conjugate, observed methionine oxidation was strongly influenced by the sample preparation procedure. In other antibodies, variability of observed methionine oxidation was attributed to on-column oxidation, which produced a broad and noisy peak that interferes with automated peak integration. EDTA flushing reduced this feature, implicating exposure to metal ions. Conclusions: While advances continue to address many MAM challenges, artificial oxidation remains unpredictable and constitutes a major obstacle to robust implementation in regulated QC environments. Enhanced control strategies and further research are urgently needed to ensure reliable therapeutic protein analysis. Such control strategies include consumable qualification and change control, system suitability/trending using a reference standard, metal management across LC flow path/column lifecycle, reduction of trifluoracetic acid (TFA) exposure, data analysis to safeguard excessive on-column oxidation, etc. Full article

The concentration of heavy metals in the environment has been steadily increasing, raising concerns about their adverse effects on ecosystems and human health. Fine-grained particulate matter is of particular concern due to its enhanced mobility, bioavailability, and potential for inhalation exposure. Facilities involved in the mechanical processing of electronic waste (e-waste) represent a significant potential source of metal-containing fine particles. In this study, crushed e-waste components containing precious metals were separated into particle-size fractions ranging from 3.0 to 0.15 mm using a vibratory sieving system. The elemental composition of the individual fractions was determined by energy-dispersive X-ray fluorescence spectrometry (ED-XRF), while the spatial distribution of selected metals in fine fractions was further investigated using scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM–EDS). The results demonstrate that e-waste contains a wide range of heavy non-ferrous metals whose distribution is strongly dependent on particle size. A pronounced enrichment of metals was observed in the finest fractions, particularly below 0.25 mm. Compared to the coarse fraction (>3 mm), the zinc concentration increased by approximately one order of magnitude, while chromium, nickel, and cadmium exhibited increases of up to approximately 20-fold. Lead showed particularly high enrichment, reaching approximately 2 wt.% in the finest fraction (<0.15 mm), corresponding to nearly fiftyfold enrichment relative to the coarse fraction. Tin concentrations also increased markedly, in some cases by up to two orders of magnitude. Trace amounts of arsenic and selenium were detected in the finest fractions, whereas mercury was not detected. The combined ED-XRF and SEM–EDS results confirm that fine-grained e-waste fractions are the dominant carriers of hazardous metals and respirable particles generated during mechanical processing. These findings highlight the dual character of fine fractions as both a critical environmental and occupational risk and a potentially valuable secondary resource. The study emphasizes the importance of controlled handling, effective dust management, and targeted processing strategies to minimize human exposure while enabling efficient recovery of valuable metals from e-waste. Full article

Tungsten is an extremely durable metal with a wide range of industrial applications and its toxicity is relatively low, although chronic exposure to its compounds can lead to adverse health effects. This paper proposes a method for the determination of trace amounts of tungsten using cathodic stripping voltammetry (CSV). A hybrid structure based on a mixture of multi-walled carbon nanotubes and spherical glassy carbon was used as the working electrode, on the surface of which a film of lead was formed during the measurement to increase the efficiency of the determination. A comprehensive optimization of the analytical parameters, including accumulation potential and time, signal recording conditions and electrolyte solution composition, was carried out to maximize sensitivity and improve the signal-to-noise ratio. The method developed achieved a detection limit for tungsten of 3 × 10⁻¹⁰ mol L⁻¹, demonstrating its high sensitivity. The working electrode showed selectivity, signal reproducibility and resistance to the presence of potential interferences. The reliability and applicability of the proposed solution were confirmed by applying the method to the analysis of real environmental samples and certified reference materials, with satisfactory results. The presented analytical procedure represents a promising tool for the routine determination of tungsten in complex real matrices. Full article

Trace metals are persistent stressors in coastal ecosystems, yet most marine algal toxicity assessments still rely on freshwater model species and growth-based endpoints that provide limited mechanistic resolution. Here, we quantified the sensitivity of two ecologically contrasting marine diatoms—the benthic Cylindrotheca closterium and the planktonic Thalassiosira weissflogii—to ten environmentally relevant metals using a dual-endpoint approach that integrates chlorophyll fluorescence (photosystem function) and Nile Red-based lipid-body fluorescence (metabolic reallocation). Fluorescence-based EC₁₀ values revealed distinct species- and metal-specific patterns, with C. closterium consistently responding at lower concentrations and Hg producing the strongest inhibition in both species (EC₁₀ ≈ 0.04–0.06 mg L⁻¹). Lipid-body accumulation detected earlier metabolic disturbance for several metals, particularly Hg, As, Cr(VI), and Cd, and frequently occurred at concentrations where fluorescence remained minimally affected. These sequential thresholds indicate that pigment impairment and metabolic reallocation represent mechanistically distinct stages of the cellular stress response that differ among metals and between diatom guilds. Comparison with published toxicity data shows that the dual-endpoint sensitivities observed here fall within, or slightly above, the upper range of reported microalgal responses, underscoring the pronounced susceptibility of benthic diatoms to redox-active and thiol-reactive metals. The strong agreement between fluorescence-based EC values and traditional growth-derived benchmarks for key metals further supports fluorescence as an operationally efficient endpoint suitable for integration into emerging ISO marine algal bioassays. Overall, this study demonstrates that pairing a rapid functional marker with a mechanistically informative metabolic biomarker enables metal-specific toxicity fingerprinting and provides an ecologically grounded basis for incorporating benthic diatoms into coastal metal risk assessment frameworks. Full article

Platinum group elements (PGE) are six rare highly siderophile metals which have similar chemical characteristics and occur together in mineral deposits: platinum (Pt), palladium (Pd), rhodium (Rh), ruthenium (Ru), iridium (Ir) and osmium (Os). In nature, they tend to exist in a metallic state or bond with sulfur and arsenic and occur as trace accessory minerals predominantly in mafic and ultramafic rocks. High industrial demand together with their scarcity in crustal rocks has been reflected in their inclusion in 2025 US Government’s List of Critical Minerals, European Union’s List of Critical Raw Materials and Mongolian List of 11 Critical Minerals. Although Mongolia is not currently a producer, it hosts four types of potentially economic PGE deposits: (1) Podiform chromitites associated with ophiolites; (2) Ni-Cu-PGE sulfide mineralization of rift-related mafic–ultramafic intrusions; (3) Alaskan–Uralian type arc related zoned mafic–ultramafic intrusions; and (4) Placers. Particularly promising are Permian Ni-Cu-PGE sulfide bearing mafic–ultramafic intrusions of the Khangai large igneous province which bear resemblance to mineralized Permian intrusions in Russia (e.g., Norilsk-Talnakh) and N.W. China (e.g., Kalatongke; Tarim basin). In addition, sub-economic ophiolite-hosted PGE mineralization can be extracted as a by-product during chromite mining. There is also the potential for PGE recovery as a by-product in existing gold placer operations in areas hosting ophiolitic massifs and Alaskan–Uralian type intrusions. Mongolia is a promising frontier for PGE exploration and mining. Full article

Cholestasis in children is characterized by impaired bile flow that disrupts hepatic metabolism, nutrient homeostasis, and effects trace element balance. This narrative review summarizes current evidence on the metabolism, biological functions, and clinical implications of key trace elements—zinc, selenium, copper, and manganese—in pediatric cholestatic liver disease. The liver regulates trace element absorption, intracellular trafficking, storage, and biliary excretion; cholestasis alters these processes, leading to deficiencies or toxic accumulation. Zinc and selenium deficiencies are common and contribute to impaired growth, immune dysfunction, oxidative stress, and delayed hepatic regeneration. Conversely, reduced biliary excretion promotes copper and manganese accumulation, potentially exacerbating liver injury and causing manganese-related neurotoxicity. Recent advances in understanding metal-specific hepatic transporters and trafficking pathways have provided mechanistic insight into these alterations. Management strategies emphasize individualized supplementation, monitoring during enteral and parenteral nutrition, and prevention of deficiency and toxicity. Precision-based nutritional approaches may improve outcomes in pediatric cholestatic liver disease. Full article

The recurrent influx of pelagic Sargassum spp. along Caribbean coastlines poses a significant environmental challenge while offering potential as a resource-recovery agricultural input. However, agricultural reuse of Sargassum biomass raises concerns regarding salinity and trace-metal distribution within the soil–plant–food continuum. This study evaluated the short-term elemental response to a Sargassum-Based Liquid Biofertilizer (SBLB) produced via controlled anaerobic fermentation, using tomato (Solanum lycopersicum L.) grown under greenhouse conditions. Raw biomass, fermented biofertilizer, irrigation water, soils, vegetative tissues, and fruits were chemically characterized. Elemental concentrations were quantified by ICP–OES and ICP-MS and treatment effects were analyzed using one-way and two-way ANOVA (p < 0.05). Anaerobic fermentation resulted in lower measured concentrations of sodium, arsenic, and selected trace elements in the liquid fraction relative to raw biomass. SBLB application increased soil macronutrient availability (N, P, K, Ca, Mg), while soil trace-metal concentrations remained within international reference ranges during the experimental period. Metals of concern (As, Cd, Pb, Ni, Cr) showed no detectable short-term enrichment in soils, vegetative tissues, or fruits relative to controls. In tomato fruits, arsenic, cadmium, and lead were below the limit of quantification across all treatments. Within the experimental timeframe, SBLB application was not associated with detectable trace-element accumulation in the soil–plant system. Long-term field studies and detailed soil physicochemical characterization are required to evaluate cumulative effects under repeated applications. Full article

Portable Buddhist shrines refer to small-scale mobile or assembled shrines, typically made of wood, stone, clay, and metal. They were initially used as temporary ritual sites or ornamental attachments for temples and stupas, later becoming independent objects of devotion. This art form, the origins of which can be traced to ancient India and later diverse regional traditions, has been discovered in significant quantities along the Silk Road and neighboring regions. Previously, scholarly attention centered primarily on exquisite wall shrines, stupa-shaped shrines, and stele-shaped shrines. However, when factors such as the spatial arrangement and ritual functions of mobile ritual sites are taken into account, along with the materials and techniques employed in creating Buddhist shrines, artifacts such as badge-style bronze Buddha statues, painted silk banners, and wooden panel paintings may also be classified as portable Buddhist shrines. Accordingly, portable Buddhist shrines can be divided into three forms: pedestal, hanging, and open–close or mother–child. A key reason for this expanded classification is that all such forms are functionally and stylistically linked to large-scale cave temples. Moreover, these shrines share a common visual grammar, defined by the dynamic integration of images and texts and the mutual imitation and complementarity of statue and painting. This represents a quintessential example of cross-cultural dissemination and the coexistence of local traditions in Buddhist art. Full article

This study evaluated the effects of fly ash (F) and effective microorganisms (EM) on nutrient dynamics and heavy metal transformations during vermicomposting of camel manure (CM). Four treatments (CM, CM + F, CM + EM, and CM + F + EM) were arranged in a completely randomized design and monitored over 12 weeks. Significant (p < 0.05) treatment and time interactions were observed for pH, NH₄-N, Mn, Pb, and Mo. The addition of EM resulted in a greater decline in pH compared to other treatments. After 12 weeks, Olsen P increased from 300.62 to 398.71 mg/kg in CM + EM, while NH₄-N increased markedly from 22.74 to 86.62 mg/kg. In contrast, NO₃/NO₂-N declined in EM-amended treatments but increased in the control and CM + F. Trace metal concentrations generally increased due to mass reduction during vermicomposting yet remained within internationally acceptable limits. Germination index (GI) values varied significantly among crops and treatments, ranging from phytotoxic to non-phytotoxic responses. Although CM + EM produced superior nutrient enrichment, several vegetables exhibited GI values below 50%, indicating potential phytotoxicity for sensitive crops. In case of established crops for which nutrient supply outweighs early phytotoxic concerns, CM + EM represents the most agronomically beneficial option. Future studies should explore blending CM + EM and CM + F with stabilizing amendments such as biochar to optimize nutrient availability while minimizing salinity and phytotoxic risks. Full article

Chronic exposure to heavy metals poses significant health risks. This study analyzed the concentrations of toxic (Cr, Pb, Cd, Ni) and essential (Cu, Zn, Se, Mn) elements in autopsy samples (the frontal pole area of the brain, the 6th intercostal space of the liver, and lungs (average of left and right lung samples) from 45 residents of South-Eastern Poland using ICP-MS. The aim was to determine the average body burden and organ-specific accumulation in a moderately industrialized region. HDBSCAN clustering revealed highly homogeneous elemental profiles, suggesting a unifying influence of local environmental factors. The liver acted as a metabolic hub, showing preferential sequestration (p < 0.0001) of essential elements (Zn, Se, Mn, Cu) regulated by homeostatic mechanisms. Toxic metals exhibited ‘metabolic trap’ patterns, particularly Cd and Pb in the liver and Cr in the lungs, due to their long biological half-lives. Strong positive correlations (Se–Zn, Se–Cu) indicated integrated antioxidant responses, while toxic pairs (Cr–Ni, Pb–Cd) suggested shared exposure pathways and molecular mimicry via transporters such as DMT1. Results confirmed long-term bioaccumulation, with toxic elements in the brain remaining below 0.25 µg/g. In the lungs, the accumulation hierarchy (Pb > Mn > Cd > Cr) reflected inhalation exposure. These findings emphasize the role of organ-specific sequestration in assessing long-term environmental exposure. Full article

The elemental composition of the vitreous humor may reflect physiological and pathological processes occurring in the eye. The objective of this study was to provide a complex multielemental analysis of human vitreous humor. Vitreous humor samples (n = 57) were collected post-mortem during autopsies. Inductively coupled plasma mass spectrometry (ICP-MS) was employed to quantify micro-, trace-, ultra-trace, and toxic elements. The study showed the occurrence of elements at the ppm (Na, K, P, Ca, Mg), ppb (Al, Rb, Zn, Fe, Sr, Cu), and ppt (Ce, La, Nd, Tb) levels. Hierarchical clustering using Ward’s method and k-means analysis revealed four distinct clusters, including two major clusters representing the baseline macro- and microelement profile characteristic for the studied population. Correlations between elements revealed statistically significant (p < 0.05) positive and negative correlations between elements with (I) chemical similarity Ce-La, Cs-Rb, Rb-K, Ca-P, Zn-Cu, and Cs-K; (II) a possible common environmental origin, Cd-P, and Rb-P; (III) involvement in similar biological processes as K-P; and (iv) a common geochemical origin and similar biological functions, i.e., Se-Zn. The study identified several quantitative trends in the demographic and medical characteristics of the participants. Alcohol users had significantly higher Zn concentrations than non-alcohol users; women had significantly higher Ca concentrations than men; higher BMI correlated positively with Cs and negatively with Be and Cr levels; and Cu, Sb, Cd, Se, and Ca concentrations increased with age. The presence of several toxic and potentially toxic elements was identified in the vitreous body: Al (>10 ppb); Cd, Cr, Pb, Ni, Mn; and Ba (<10 ppb); As, Hg, Sb, Tl, Bi, Be (<1 ppb). The study showed that, within a given geographic region, the accumulation profiles of toxic metals are quite homogeneous, indicating common sources of exposure. Full article

Neural interfaces created using thin-film fabrication rely primarily on conductive metal traces for electrical interconnects. Here, we explore the use of tantalum (Ta) metal interconnects as a replacement for noble-metal interconnects such as Au, Pt or Ir. Ta has been investigated previously for interconnect metallization in flexible silicon ribbon cables, but the structure and properties of tantalum for neural device metallization have not been extensively reported. In the present work, Ta metal was sputter-deposited onto amorphous silicon carbide (a-SiC), with and without a base titanium (Ti) adhesion layer, and investigated as interconnect metallization. In the absence of a Ti adhesion layer, resistivity measurements revealed a factor of six difference between Ta resistivity depending on the presence of the Ti base layer, with direct deposition on a-SiC nucleating high resistivity β-Ta (ρ = 197 ± 31 µΩ·cm, mean ± standard deviation) and Ta deposited on Ti nucleating low resistivity α-Ta (ρ = 35 ± 6 µΩ·cm). X-ray diffraction confirmed the existence of the two crystal structures. Ta feature sizes of 2 µm were created using photolithography and reactive ion etching (RIE). Finally, planar microelectrode array test structures using α-Ta and Au trace metallization with low-impedance ruthenium oxide (RuO_x) electrodes were fabricated and investigated by cyclic voltammetry (CV) and current pulsing in saline. These devices underwent 500 CV cycles between −0.6 and +0.6 V without evidence of degradation. In response to charge-balanced, biphasic current pulses at 4 nC/phase, a 21 mV increase in access voltage was observed with α-Ta metallization compared to Au. These results warrant further investigation of Ta as thin-film metallization interconnects for neural interface devices. Full article

The Cândești necropolis is currently the largest excavated Bronze Age necropolis in Romania, with approximately 800 graves. Notably, one grave from an earlier phase of the Monteoru culture (c. 2200–1850 BC) contained a remarkable necklace composed of 22 perforated gastropod shells and a metal pendant. Our investigation adopted an integrated approach, including taxonomic identification, taphonomic, technological and functional analyses, experimental studies, and physico-chemical investigations (Fourier Transform Infrared Spectroscopy and Raman spectroscopy) of the pigment traces present on the shells’s surface. For the metal pendant, X-Ray Fluorescence analysis was conducted to ascertain its elemental composition. The combined analysis yielded unexpected insights: the shells, belonging to the genus Conus, originated from the Mediterranean region. The perforations were not the result of anthropic intervention; rather, they were the result of natural processes, indicating that the shells were collected from thanatocoenoses. The shells were assembled into the necklace using a thread colored with a red pigment. The perforations show signs of prolonged use, suggesting that the necklace was not only a funerary offering. In conclusion, our study indicated that these exotic shells were collected post-mortem already perforated through a rubbing process in the seashore sediments, transported to the site from a distance, and prior to the death of the owner, had been previously worn as personal adornment before being deposited as grave goods. Full article

Magnetite is extensively developed within various alteration zones of the mining district. Some magnetite is closely associated with copper mineralization, possessing significant research value. The Duobuza Cu (Au) deposit is a typical porphyry-type deposit within the Bangong Co-Nujiang metallogenic belt and was the first porphyry Cu-Au deposit discovered in the Duolong copper–gold ore district. Currently, this deposit contains copper resources exceeding 3 million tons @0.46%, with associated gold resources exceeding 80 tons @0.19 g/t. This study focuses on magnetite from the Duobuza deposit. Through field geological logging and microscopic identification combined with electron microprobe analysis (EMPA) and in situ LA-ICP-MS testing, mineralogical and mineral chemical research on magnetite is conducted. This research aims to elucidate the genesis of magnetite in the Duobuza deposit and its implications for mineral exploration. Five magnetite types with different occurrences can be distinguished in the Duobuza deposit: Mt₁ is magmatic magnetite; Mt₂, Mt₃, Mt₄, and Mt₅ are hydrothermal magnetite, with Mt₅ being closely associated with copper mineralization. Mt₁ is relatively enriched in Ti, V, Al, and Cr but depleted in Mn and Si; Mt₂ is relatively enriched in Ti and Al but depleted in Si and Cr; Mt₃ is relatively enriched in Al but depleted in Mg; Mt₄ is relatively enriched in Ti, Al, V, Zn, and Mn; and Mt₅ is relatively enriched in Mg, Si, Ti, Al, Mn, and Zn but depleted in Cr. Based on the Al + Mn vs. Ti + V discrimination diagram, magnetite formed in a medium- to high-temperature environment, with hydrothermal magnetite Mt₄ forming at the lowest temperature. Vanadium (V) content can be used to estimate the oxygen fugacity (fO₂) during mineralization. Mt₁ exhibits the highest V content, indicating relatively low oxygen fugacity, whereas Mt₄ shows the lowest V content, suggesting relatively high oxygen fugacity. Mt₅ has a higher V content compared to other early-stage hydrothermal magnetites, suggesting that a lower fO₂ formation environment favors the precipitation of metal sulfides in the mining district. Trace element analysis of magnetite from the Duobuza, Bolong, and Naruo mining districts reveals that magnetite from all three deposits is enriched in Si and Al and depleted in Ca and Ni. Magmatic magnetite from the Naruo and Duobuza deposits exhibits similar elemental distribution patterns. Hydrothermal magnetite from the Duobuza deposit shows significantly higher Ti and V contents compared to magnetite from the Bolong and Naruo deposits. Full article