Zn Concentrations Research Articles

Magnetron sputtered Zn-Ta2O5 thin films for electronic, thermoelectric, and optical applications

In the current study, the optical and electronic properties of Zn-Ta2O5 have been investigated as a potential optoelectronic material. Theoretically, the density functional theory was employed to pure and Zn doped Ta2O5 compositions using the Wien2k code. For experimental investigations uniform thin films were fabricated by magnetron co-sputtering technique on the silicon substrate. The optical, thermoelectric, electronic, and morphological properties were studied by relating the outcomes of simulations and experimental results providing the correlation among the findings. Graphs of the total density of states and partial density of states revealed the hybridization between the dopant and host orbitals. The p-d hybridization of O and Ta atoms was shown by the density of states. Structural studies reveal the growth of primary phase identified as orthorhombic Ta2O5. The grain growth of the Zn-Ta2O5 thin films gradually increase as the Zn content was increased and led to more compact film formation. Zn incorporation improves the thermal transport properties by increasing the Seebeck coefficient and reducing thermal conductivity. Band gap values were reduced by increasing the Zn concentration and recorded value was observed as 3.07 eV for Ta2O5 and 1.77 eV for maximum zinc concentration. Optical characteristics are measured in relation to photon energy which shows enhancement by the Zn doping. The outcomes of the current study manifest that these materials provide great potential for thermoelectric and optoelectronic applications.

Heavy metal accumulation and interaction dynamics in Brachidontes pharaonis: a bioindicator study in the Red Sea.

This work evaluates utilizing the native mussel Brachidontes pharaonis as a bioindicator and sentinel organism for monitoring heavy metals Cu, Zn, and Cd along the Red Sea coast of Egypt. Samples were collected from four coastal locations, and the concentrations of heavy metals in the mussels' tissues, shells, seawater, and sediments were analyzed. Subsequently, bioassay experiments were conducted by exposing the organisms to single, binary, and tertiary metal mixtures, and the accumulation of heavy metals was determined to elucidate the dynamics of metal-metal interactions. Field samples revealed significant variations in heavy metal concentrations in the mussels' soft tissues across different locations, with Zn ranging from 58.1 to 121.0µg/g dw (dry weight), Cu ranging between 18.3 and 36.7µg/g dw, and Cd ranging from 0.3 to 1.04µg/g dw. Conversely, the shells exhibited minimal spatial variations, with much lower contents of Cu (ranging from 1.9 to 2.8µg/g dw) and Zn (ranging from 1.8 to 1.9µg/g dw). However, the shells accumulated Cd at higher levels (ranging from 1.4 to 2.1µg/g dw) compared to the soft tissues. Following a 96-h bioassay experiment, the soft tissues displayed a linear accumulation of metals with increasing exposure dose, with Cd showing the highest accumulation rate (approximately threefold) followed by Zn (twofold) and Cu (1.7-fold). In binary and tertiary exposures, the metals exhibited a general antagonistic interaction, affecting each other's accumulation. On the other hand, the accumulation of heavy metals in the shells after the 96-h bioassay exposure did not follow a consistent linear pattern, suggesting that accumulation during this short experimental period occurs primarily through adsorption rather than the biological pathway.

Variability in mineral composition of Canadian lentil genotypes

Lentils are a good dietary source of essential minerals for the proper functioning of the human body. We evaluated 34 cultivars and elite lentil lines representing the breadth of the Canadian breeding program. Trials were established in 10 site-years across Saskatchewan. Concentrations of 27 minerals were quantified with an inductive coupled argon plasma emission spectrometer in whole and dehulled lentil seeds. Lithium (Li), vanadium (V), chromium (Cr), cobalt (Co), arsenic (As), silver (Ag), cadmium (Cd), tin (Sn), lanthanum (La), mercury (Hg), and lead (Pb) had concentrations below the quantification limit and were excluded from further analysis. The effects of site year, tissue type (whole and dehulled), and lentil genotypes were analyzed using a mixed model. Mineral concentrations of iron (Fe), zinc (Zn), magnesium (Mg), sodium (Na), potassium (K), phosphorus (P), sulfur (S), manganese (Mn), copper (Cu), molybdenum (Mo), boron (B), nickel (Ni), selenium (Se), aluminum (Al), and barium (Ba) was different among genotypes and across environments. Most minerals except Cu had significantly different concentrations between whole and dehulled seeds. Ca, Fe, Mg, Mn, B, Al, and Ba were more concentrated in whole seeds, while K, S, and Ni were higher in dehulled seeds. Among the 34 genotypes, CDC Impala had the highest Fe, Zn, K, P, S, and Cu concentrations. Lentil genotypes with a higher composition of several minerals could be a starting point for enhancing mineral composition in lentils.

Effect of zinc management on yield, nutrient content, and acquisition of zero-tilled wheat (Triticum aestivum)

A field experiment was conducted during the winter (rabi) season 2018–19 and 2019–20 at Khalsa College, Amritsar, Punjab to find out the effect of soil and foliar application of ZnSO4 .7H2 O on zero till wheat. The experi- ment was conducted in a randomized complete block design with three replications. Treatments were control (noZn), soil application of 12.5, 25, 37.5, 50 kg/ha zinc sulfate heptahydrate (ZnSO4 .7H2 O), and foliar application of 0.5% Zn as one spray at heading initiation (5% ear emergence), one spray at 100% heading (complete ear emergence) and two sprays at heading initiation and 100% heading with a recommended dose of fertilizer. Results showed that the soil application of 50 kg Zn/ha with two foliar sprays of 0.5% zinc sulfate heptahydrate at heading initiation and 100% heading produced the highest yield attributes and grain yield of wheat. Application of 50 kg Zn/ ha with two foliar sprays of 0.5 % Zn at heading initiation and 100% heading registered ~25% higher grain yield over control. Grain Zn content (41.77ppm) percent increase was 33.9 with 50 kg Zn/ha with two foliar sprays of 0.5 % zinc at heading initiation and 100% heading over control (31.20 ppm).Likewise, application of 50 kg Zn/ha with two foliar sprays of 0.5 % Zn at heading initiation and 100% heading recorded the highest net returns among the Zn treatments. Overall, soil application of 50 kg Zn/ha with two foliar sprays of 0.5 % zinc at heading initiation and 100% heading improved the yield, uptake, and profitability of zero-tilled wheat in zinc-deficient soils.

Stable isotopes analysis combined with X-ray absorption spectroscopy reveal the fate of organic waste-borne copper and zinc in amended soils

Copper (Cu) and zinc (Zn), two potentially toxic trace elements, are commonly abundant in organic wastes (OWs) recycled in soils as fertilizer. Yet current knowledge on the long-term behavior and fate of Cu and Zn in soil following OW spreading is scant. We addressed this issue by studying the fate of OW-borne Cu and Zn in amended soils from four different long-term field experiments. By combining the stable isotope analysis and X-ray absorption spectroscopy, we identified changes in Cu and Zn concentrations, speciation and isotopic compositions in the amended soils only when OW had been applied at high rates over long periods. Under these conditions, we highlighted that: (i) all OW-derived Cu and Zn had accumulated in the topsoil layer regardless of the soil and OW type; (ii) the amended soil isotopic signatures were the result of the mixing of OW-borne and natural Cu and Zn; and (iii) Cu and Zn exhibited distinct speciation patterns in amended soils. Indeed, the unprecedented persistence of OW-borne crystallized Cu(I)-sulfide in the amended soils contrasted with the complete transformation of pig slurry-borne nanosized Zn-sulfide or household compost-derived amorphous Zn phosphate and Zn complexed by organic matter.

Geochemical fractionation of trace elements in ostreid and gastropod shells: A potential proxy for heavy metal pollution in Ghana’s coastal environment

The content of trace elements from Crassostrea tulipa (Ostreidae, Bivalvia) from four localities (Pra Estuary, Densu Estuary, Kpone Beach, and Anyanui Creek) along the coast of Ghana has been used as a bioindicator of environmental pollution. The lowest values of heavy metals correspond to the Crassostrea shells from Densu Estuary and Anyanui Creek, whereas the highest contents are recorded in the shells from Pra Estuary and Kpone Beach. Densu Estuary and Anyanui Creek are located in areas not affected by major industries, and only Densu is located in a densely urbanized setting. Crassostrea shells from Densu Estuary are only enriched in Ni. However, the Total Organic Carbon content of the sediments of the Densu Estuary indicates anthropogenic organic pollution not evidenced by the composition of Crassostrea shells. The Crassostrea shells from the Pra Estuary show enrichment in most of the analysed trace elements (Li, Be, V, Cu, Cr, Zn, Ga, Y, Sn, Pb, U, Th, ∑REE, and As) compared with other studied sites. This enrichment is related to heavy metals influx to the Pra River by the mining activities, extensive forest clearance, and loss of soil minerals. The Crassostrea shells from Kpone Beach present comparatively high content of some trace elements (Be, Ba, Cu, Zn, Nb, Pb, and REE). The metal pollutants are related to the input of the Heavy Industrial Area of Tema (located around 3.5 km west of Kpone Beach) and urban effluences from the Greater Accra Region. The high content of Ba, Cu, Zn, and Pb in Crassostrea is directly related to high phytoplankton productivity (mainly for diatoms) linked to the input of trace metals transferred into the marine food webs. In addition, some analyses of gastropod shells from Kpone Beach indicate that Cerithium and Nerita are more sensitive to accumulating Ni and As than Crassostrea. The values of trace metals from the Crassostrea shells of the Densu Estuary and Anyanui Creek are comparatively low. Considering the role of Crassostrea shells as bioindicators for heavy metals pollution, the less polluted localities are Anyanui Creek and Densu Estuary, whereas Pra Estuary and Kpone Beach are affected by anthropic activities such as mining, urban effluents, and industry.

Assessment of potentially toxic element contamination in wetland sediments of Boracay Island, Philippines

Boracay Island, Philippines, famous for its white sand beaches, has wetlands increasingly threatened by human activities. This study evaluated the ecological state of Boracay Island's wetlands and assessed the consequences of anthropogenic activities on sediment quality. Results showed that sediments from Wetland Nos. 3 and 4 have higher concentrations of potentially toxic elements (PTEs) than Wetland No. 1. Comparative analysis with other Southeast Asian wetlands revealed that Boracay's sediments contain the highest average values of As, Cd, Cu, Ni, Zn. Enrichment factor values suggest that the moderate enrichment of Cd, Cr, Cu, Mo, Pb, and Zn in the wetland sediments can be attributed to anthropogenic activities on the island. Elevated concentrations of Cr, Cu, and Zn above interim sediment quality guidelines indicate occasional adverse biological effects on aquatic biota. These findings provide a crucial baseline for future pollution monitoring and highlight the need for ongoing conservation efforts in Boracay's wetlands.

B-164 Comparison of Analytical Performance of Two Processing Methods for Measurement of Zinc and Copper on Triple Quadrupole Inductively Coupled Plasma Mass Spectrometer

Abstract Background Copper (Cu) and zinc (Zn) are essential cofactors of enzymes involved in several metabolic processes required for the development of tissue structures and immune response, especially in pediatrics and pregnant women. Triple quadrupole inductively coupled plasma mass spectrometer (ICP-QQQ) enables simultaneous precise quantification of multiple elements with high throughput, sensitivity, and specificity. Samples are introduced into ICP-QQQ as a liquid and converted to fine aerosol with the help of a nebulizer and spray chamber. The precision and sensitivity of measured metals are dependent on the sample preparation thus, this study focuses on comparing the analytical performances between two sample preparations: 0.5% nitric acid (HNO3) as the only diluent (Diluent A) versus a combination of 0.5% HNO3 along with 1% ethanol, 0.5% Ammonium hydroxide, 0.02% TritonX-100, and 0.1% HNO3 (Diluent B) for Cu and Zn metal analysis in serum using ICP-QQQ. Methods Twenty deidentified randomly selected patient serum samples were prepared with either diluent A or diluent B and analyzed by ICP-QQQ (Agilent 8900). Data were analyzed using EP Evaluator. Bland-Altman analysis was used to determine the agreement between the two sample preparations. Deming regression analysis was used to determine other analytical performances, such as the proportional and constant bias of Zn and Cu concentration. Results There was a bias of -4.8 and -3.0 between the two sample preparation methods when analyzing Cu and Zn, respectively. The mean of Cu-Diluent B versus Cu—Diluent A was 125.2 ± 28.3 µg/dL and 120.4 ± 29.8 µg/dL, respectively, with a slope of 1.070. Conversely, the Zn comparison study shows a lower slope (0.769) with a mean of 71.0 ± 20.5 and 68.0 ± 16.1 µg/dL for Zn-Diluent B and Zn-Diluent A, respectively. Conclusions Samples prepared with nitric acid solution only (Diluent A) appeared to show negative bias compared to Diluent B solution containing triton-X for both metals. However, the bias is within the total allowable error for zinc and copper. Importantly, Zn-sample analysis with diluent A (HNO3 only) shows a 23% proportional bias, which is absent with copper sample analysis. A larger study is needed to further compare several methods of sample preparation in ICP-QQQ analysis while leveraging simple preparation without compromising analytical sensitivity. Overall, this study shows that both methods of sample preparation can be effectively used in the ICP-QQQ analysis of serum copper and zinc.

Variation of grain zinc, phytate concentration and phytate : Zn molar ratio in unpolished and polished rice affected by foliar zinc application among Thai rice varieties

ABSTRACT This study evaluated the variation in grain yield and Zn concentration in rice after foliar application of Zn and the impact on its phytate : Zn molar ratio among 21 rice varieties. Rice varieties were grown under field conditions using a randomized complete block design with four replications over two cropping years in 2020 and 2021 during the rainy season. Foliar Zn application varied grain yield from −26.0 to 13.6% in 2020 and −14.7 to 30.4% in 2021 compared with non-foliar Zn. Grain Zn was varied from 0.5 to 31.1% in 2020 and from −5.9 to 47.8% in 2021 in unpolished rice and from 9.4 to 47.0% in 2020 and from 8.2 to 163.0% in 2021 in polished rice. The phytate : Zn molar ratio was decreased when foliar Zn was applied to the unpolished and polished rice, with a lower ratio in the polished rice. The phytate : Zn molar ratio decreased exponentially with increasing grain Zn concentration in the unpolished rice, while decreasing linearly with increasing grain Zn concentration in the polished rice. The results of this study suggest that foliar Zn application is a promising way to improve the grain Zn concentration and decrease the phytate : Zn molar ratio, thus being beneficial for human diets, but the effects of rice variety, cropping season, and the polishing process should be considered.

Co-occurrence of microplastics and microparticles containing Cu and Zn and other heavy metals in sea-surface microlayer in Osaka Bay, Japan

Antifouling biocides such as Cu, Zn, and organic compounds not only inhibit adhesion of sessile organisms on ship hull but also possess toxicity to non-sessile organisms in marine environment. Thus, we firstly investigated the heavy metals and polymer types of anthropogenic microparticles (MPs) floating in the sea-surface microlayer (S-SML) in Osaka Bay. 7 types of MPs containing different metals (Cu, Cu-Zn, Zn, Ti, Sn, Ba and Fe-Mn-Ni) were found. The polymer type for 97.8 % of Cu and Cu-Zn MPs (41 samples) and 52.6 % of Zn MPs (19 samples) was acrylic resins which are widely used as binders in contemporary antifouling paints for ships; concentrations of 511–54,000 mg/kg for Cu and 95.1–13,200 mg/kg for Zn were found in these MPs. The high metal concentrations found the co-existence of acrylic polymers point towards an origin from antifouling paint particles (APPs). Furthermore, to quantify Cu and Zn concentrations in these MPs based on X-ray fluorescence spectroscopy (μ-XRF), calibration curves obtained from standard paint particles containing different Cu and Zn concentrations and different particle sizes made with similar matrix used in commercial antifouling paint were firstly established, according to which highly reliable Cu and Zn concentrations in MPs were obtained.

Sonochemical synthesis of mesoporous ZnyCd1-yS quantum dots: Composition-dependent optical, electrical, dielectric, and hydrogen-generation characteristics

Mesoporous ZnyCd1-yS quantum dots (QDs) with mixed cubic–hexagonal phases prepared by sonochemical technique at varying Zn content. Incorporating Zn ions in the CdS lattice reduced the crystalline size and enhanced the corresponding surface areas at increasing Zn contents. The increase of Zn content in ZnyCd1-yS QDs increased the bandgap from 2.52 eV to 3.83 eV and enhanced the corresponding Urbach energy from 72 meV to 279 meV. ZnyCd1-yS QDs exhibited small electrical activation energies ranging from 249 mV to 361 mV. The effect of Zn content on the catalytic activity of ZnyCd1-yS QDs toward hydrogen production through NaBH4 hydrolysis was investigated at different temperatures. Ternary alloys ZnCdS QDs exhibited higher catalytic activity than pure ZnS and CdS QDs, with Zn0.5Cd0.5S QDs displaying the highest hydrogen generation rate of 96 mL∙min−1∙g−1. The increase of reaction temperature from 30°C to 60°C enhanced the rate constant of hydrogen production from 0.071 to 0.36 min−1. Based on the pseudo-first-order equation, the estimated apparent activation energy of Zn0.5Cd0.5S QDs was 45.3 kJ∙mol−1. Overall, the obtained results underscored the potential of ZnyCd1-yS QDs as promising catalysts for hydrogen generation.

Heavy metal migration and enrichment in desulfurization wastewater during low-temperature triple effect evaporation process

Zero discharge of desulfurization wastewater from coal-fired power plants has become important. Desulfurization wastewater and gypsum from different stages of the low-temperature triple-effect evaporation process of a coal-fired power plant were collected and investigated. The results showed that after low-temperature triple-effect evaporation, the concentrations of Na+, Mg2+, K+, and Cl− in the desulfurization wastewater increased by 7.91, 7.15, 8.49, and 8.35 times, respectively. With the progress of low-temperature triple effect evaporation process, the concentrations of As, Cd, Co, Cr, Cu, Mn, Se, and Zn in the wastewater after the triple effects were 5.85, 75.44, 1.28, 2.34, 13.66, 5.58, 8.59, and 4.35 times higher than those in the raw wastewater. Mn and Se exceeded the emission limits by 40 and 10 times, respectively. After triple-effect evaporation, the concentrations of As, Cd, Co, Cr, Cu, Pb, Se, and Zn in gypsum decreased to 46%, 26%, 66%, 41%, 35%, 97%, 39%, and 51% of the raw gypsum, respectively. Compared with that of other metal sulfates, the solubility of PbSO4 was extremely low under low-temperature conditions, and some PbSO4 precipitated during the triple-effect evaporation process, leading to a gradual decrease in the Pb concentration in the liquid phase. The mercury compounds in gypsum after the first and second effects were the same as those in raw gypsum, both of which were HgS and HgO. After third effect, the mercury compound in gypsum also included HgSO4. In addition, owing to the promoting effect of the pH of desulfurization wastewater approaching 5.50 on the generation of HgS, the proportion of HgS gradually increased, and the proportion of HgO gradually decreased from the raw gypsum to the third effect gypsum. Therefore, the stability of the mercury compounds in gypsum was enhanced. It can provide a good reference for the migration and enrichment of heavy metals in the low-temperature triple-effect evaporation process, which is beneficial for the clean production and efficient utilization of coal.

Interaction Effects of Phosphorus and Zinc Application on Their Availability and Growth of Rice (<em>Oryza sativa</em>) in an Alfisol of Sri Lanka

This study investigated the interactive effects of phosphorus (P) and zinc (Zn) application on P and Zn availability, and growth of rice (Oryza sativa) in an Alfisol. In a laboratory incubation experiment, soil samples were supersaturated with treatment solutions with all possible combinations of four P levels (0, 6, 12, and 24 mg kg-1 equivalent to 0, 10, 20, and 40 kg ha-1, respectively) and three Zn levels (0, 1.2, and 2.4 mg kg-1 equivalent to 0, 2, and 4 kg ha-1, respectively), and then allowed to air-dry. Available P and Zn contents in soil increased as the application rates were increased but P×Zn rate interaction effect was not significant. In a pot experiment, rice (var Bg 358) was grown for 10 weeks with all possible combinations of three P levels (0, 5.5, and 16.5 mg kg-1) and three Zn levels (0, 1, and 2 mg kg-1). Initial soil P was higher than the critical level (12 mg kg-1), but available Zn was below the critical level (1.5 mg kg-1). The main effect of P rate did not significantly affect the number of tillers and shoot dry matter content while Zn application decreased them. Root dry matter, and root and shoot P concentrations were significantly (P<0.05) influenced by P×Zn rate interaction effect. While, plant P uptake was significantly decreased due to P and Zn application, plant Zn uptake was not affected. Therefore, for a better growth of rice plant, the soils with high available P and low Zn contents should be carefully fertilized with P and Zn fertilizers.

Effects of Nano Silver and Indole Butyric Acid Application on Growth and Some Physiological Characteristics on Hardwood Cutting of Dalbergia sissoo Roxb

Nanosilver (NS) and indole-3-butyric acid (IBA) can improve cutting performance and subsequent growth. This study was performed in Taqtaq city in a randomized complete block design to study the effects of NS (30, 60, and 90 mg/L) and IBA (50, 100, and 200 mg/L) in addition to distilled water as a control on growth and some characteristics of hardwood cutting of Dalbergia sissoo Roxb. Application of IBA enhanced significantly buds sprouting, where the cutting treated with 50 mg/L IBA sprouted after 35.53 days. IBA at 200 mg/L increased plant leaf area significantly to 204.11 dm2 in comparison to the control cuttings (122.00 dm2). Furthermore, IBA at 50 and 200 mg/L increased the number of leaves to 194.66 and 193.00 leaves/plant, compared to control cuttings (158 leaves/plant). The lowest peroxidase activity (902.00 and 903.30 absorbing units/ g fresh leaves) was observed in the cuttings soaked in 30 and 60 mg/L NS, respectively. Both NS and IBA had a significant effect on macro and microelements in the shoot except Mg and Fe. The shoot content of elements was different in response to NS and IBA applications, whereas the high level of IBA decreased significantly K content (25.80 %) it increased significantly the shoot content of Zn (0.22%). However the lowest concentration of NS (30 mg/L) decreased significantly the Cu content (0.02 %) and increased significantly the shoot content of Mn (0.58%). Root response to NS and IBA also was different, where 90 mg/L NS increased significantly each of K (26.40%) and Zn content (0.68 %), whereas it decreased significantly the root content of Fe (8.78%). The enhancement effects of IBA were more than that of NS on most studied characteristics.

Synthesis, characterization, and biological properties of calcium and zinc based ION incorporated amorphous carbonate nanoparticles

In this study, magnesium (Mg), zinc (Zn), and strontium (Sr) incorporated amorphous calcium carbonate (ACC) nanoparticles were synthesized. Results revealed that at low Zn concentrations, Zn and Sr co-incorporated, Mg-stabilized amorphous calcium carbonate (ACMC) nanoparticles were obtained. However, at high Zn concentrations, instead of ACMC, calcium (Ca) and Sr co-incorporated, magnesium-stabilized amorphous zinc carbonate (AZMC) nanoparticles were obtained. Our results demonstrated that Mg could be used to stabilize the amorphous structure of both nanoparticles. The additive ions could be incorporated into the structure of both ACMC and AZMC without impairing their amorphous nature. The synthesized nanoparticles had an average size of about ∼30 nm. Degradation studies suggested that the degradation rate of AZMC nanoparticles could be slower compared to ACMC nanoparticles. Antibacterial tests showed that the number of colony forming units for the Ca and Sr co-incorporated AZMC nanoparticles was lower for both Staphylococcus aureus (S. aureus), and Escherichia coli (E. coli) strains compared to the control group. Cytotoxicity studies revealed that fibroblasts interacting with the ion-incorporated ACMC and AZMC nanoparticles remained viable and proliferated for up to 5 days in vitro. These results demonstrated for the first time that Zn and Sr co-incorporated ACMC nanoparticles were non-toxic, biodegradable, and possessed antibacterial properties. In addition, Ca and Sr co-incorporated AZMC nanoparticles exhibited a stronger antibacterial effect, which makes them promising candidates for antibacterial applications.

Method validation of an inductively coupled plasma mass spectrometry (ICP-MS) assay for the analysis of magnesium, copper and zinc in red blood cells

BackgroundLaboratory measurements of trace elements such as magnesium (Mg), copper (Cu), and zinc (Zn) in red blood cells (RBCs) are essential for assessing nutritional status and diagnosing metal toxicity. The purpose of this study was to develop and validate an ICP-MS method for quantifying these elements in RBCs. MethodsPacked RBCs were aliquoted and diluted in an alkaline diluent solution containing internal standards, 0.1 % Triton X-100, 0.1 % EDTA, and 1 % ammonium hydroxide. The resulting diluted specimen was analyzed using inductively coupled plasma mass spectrometry (ICP-MS) to quantitatively determine the levels of Mg, Cu, and Zn. The method underwent validation for accuracy, precision, method comparison, linearity, analytical sensitivity, and carryover. Additionally, retrospective data were analyzed, and non-parametric reference intervals were calculated. ResultsAccuracy and linearity fell within the expected range of ≤±15 % for all analytes. Within-run, between-run, and total imprecision were ≤15 % coefficient of variation. All other validation experiments met the established acceptance criteria. Retrospective data analysis was conducted on patient samples using the method. The application of Tukey’s HSD test for multiple comparisons revealed statistically significant mean differences (p < 0.05) in Mg, Cu, and Zn concentrations between all pairwise groups of age and sex, except for the mean Cu concentration in adult males versus females and the mean Mg concentrations in adult versus minor males. ConclusionsThe presented method was successfully validated and met the criteria for clinical use. Retrospective data analysis of patient results demonstrated the method’s suitability for assessing nutritional deficiency and toxicity.

Genesis of the Kateba’asu gold deposit, Western Tianshan, China: Constraints from pyrite trace element, sulfur isotope, and quartz H-O isotopes

The Kateba’asu gold deposit, situated in the Western Tianshan of China, is one of the most significant discoveries in the world-class Tianshan gold belt. The deposit features two distinct mineralization styles. The early, subordinate skarn-type copper–gold mineralization occurs in the contact zone between monzogranite, diorite, and Silurian limestone, composed of garnet, diopside, epidote, chalcopyrite, pyrite, and gold. The later, primary lode-gold mineralization is hosted in the altered monzogranite characterized by pervasive quartz-pyrite-sericite-chlorite-K-feldspar alteration and a well-develped veining systems.Pyrite is the dominant sulfide mineral related to gold mineralization in the Kateba’asu gold deposit, with four types identified: Py0 from the early skarn copper–gold mineralization, and Py1 to Py3 from the later lode-gold mineralization. All types of pyrite are homogeneous and contain very low levels of lattice-bound gold. Py0 is euhedral and fine-grained, with relatively high Cu, Au, Co, and Ni contents, and displays a magmatic sulfur isotopic signature with δ34S ranging from 0.8 to 4.3 ‰. Py1 occurs as euhedral to subhedral, coarse-grained crystals within pyrite-quartz veins with higher concentrations of Co and Ni. Py2, which develops in the quartz-pyrite veins, is medium to coarse-grained and contains elevated levels of As, Cu, Zn, and Bi relative to Py1. Py3, found in polymetallic sulfide veins of the main lode-gold stage, is anhedral and medium to fine-grained with higher contents of As, Ag, Cu, Zn, Se, Te and lowest Co and Ni concentrations compared to Py1 and Py2. The positive correlations between Au-Te, Au-Bi, Au-Cu, and Pb-Bi across all pyrite types, along with the presence of visible gold in Py3, indicate that most gold occurs as micro-/nano-sized inclusions and as fissure gold. The δ34S values of Py1, Py2, and Py3 (7.6 to 11.8 ‰, 10.1 to 12.6 ‰, and 9.8 to 12.4 ‰, respectively) were attributed to an initial magmatic source and mixed with external sulfur subsequently from the wall rocks. The H and O isotopic compositions (δDH2O = −84.1 to −93.5 ‰; δ18OH2O = 1.8 to 6.6 ‰) of quartz from the lode-gold mineralization imply that ore-forming fluids were predominantly of magmatic origin, with a additional contribution from meteoric water. Taken together, a two-episode mineralization model was proposed for the formation of the Kateba’asu gold deposit. The early skarn mineralization stage is associated with the emplacement of diorite during the Early Carboniferous. In contrast, the subsequent lode-gold mineralization, occurring between the Late Carboniferous and Permian periods, represents a overprinted magmatic-hydrothermal gold system potentially linked to a deep-seated magmatic intrusion.

How does the coupled action of freeze - Thaw and acidification affect the release of toxic elements from indigenous Zn smelting slags?

Under complicated field conditions, such as the coupled effects of freeze - thaw cycles (FTs) and acidification, the leaching behavior of potentially toxic element (PTEs) from indigenous Zn smelting slags (ZSS) was intricately connected to the mineralogy (e.g., the composition, assemblage, microstructure of mineral particles). In this study, FTs tests were carried out to explore the interactions between PTEs release and ZSS mineralogy. Subsequently, advanced characterization techniques were adopted to quantify the mineralogy and microstructure of ZSS. The results indicated that ZSS were mainly composed of silicate minerals (e.g., quartz, biotite and chlorite) and secondary Fe (III) oxyhydroxides (e.g., magnetite and limonite), accounting for 67.48% and 24.23%, respectively. The occurrence mode analysis revealed that 81.95% of As, 21.31% of Pb and 7.77% of Zn were hosted in limonite. About 37.89%, 59.34% and 34.50% of Cd, Pb and Zn were associated with carbonate bound fractions. Under FTs interacting with different pH conditions, the leaching concentrations of As, Cd, Cu, Pb and Zn did not significantly increase with the increase in FTs and pH. The microstructure damage of mineral particles in ZSS with the higher porosity was caused by both FTs and proton corrosion. More importantly, the geochemical modeling results suggested that the precipitation of hematite and magnetite might have little impacts on PTEs release under FTs and FTs with acidification. This work would provide a deeper understanding of PTEs release from smelting waste slags under complex physicochemical interactions.

Analysis of the nutritional and antinutritional contents of tubers of Agew potatoes (Plectranthus edulis) grown in the Awi Zone, Amhara regional state of Ethiopia

Plectranthus edulis is one of the most important tuberous plants, is an indigenous plant, and grows in middle- and high-altitude areas. This study investigated the proximate, antinutritional, antioxidant, and mineral compositions of P. edulis (Agew potato) grown in the Dangila, Ankesha, and Banja districts in the Awi zone of the Amhara region, Ethiopia. The proximate composition was determined via the Association of Official Analytical Chemists (AOAC) protocol. The moisture, ash, crude fat, crude protein, crude fiber, carbohydrate, phytate, tannin, TPC, TFC, and DPPH assay results ranged from 70.87 to 74.92 g/100 g, 3.92–4.58 g/10 g, 0.36–0.61 g/100 g, 6.86–9.29 g/100 g, 3.18–3.56 g/100 g, 71.79–78.81 g/100 g, 61.48–108.04 mg/100 g, 8.46–44.15 mg/100 g, 17.53–28.42 mg/g, 2.75–5.71 mg/g, and 52.94–71.49%, respectively. The concentrations of Na, P, Fe, Cu, and Zn ranged from 261.85 to 603.90 mg/kg, 82.02–251.82 mg/100 g, 23.74–65.36 mg/kg, 9.98–16.27 mg/kg, and 17.68–30.20 mg/kg, respectively. The Agew potato from Dangila had a better nutritional content than Banja and Ankesha. Agew potatoes are nutritious and medically important tuber plants used to secure food, especially in undernourished societies.

Concurrent removal of Fe(II), Cu(II), and Zn(II) cations from acid mine drainage by an industrial solid waste - steel slag: Behaviors and mechanisms

Acid mine drainage (AMD) contamination poses a severe environmental threat and is a significant risk to human health. There is an urgent need to develop environmentally sustainable and technically viable solutions for water contamination caused by heavy metals. In this study, steel slag (SS) was used as a secondary resource to concurrently remove Fe(II), Cu(II), and Zn(II) from AMD. Because of the loose and porous structure, abundant functional groups, fast sedimentation velocity, and excellent solid-liquid separation, SS showed exceptional removal performance for heavy metal ions. The adsorption kinetic data of Fe(II), Cu(II), and Zn(II) showed good regression with the pseudo-second-order model. Besides, the adsorption of Fe(II) by SS conformed to the Freundlich model, whereas the adsorption of Cu(II) and Zn(II) followed the Langmuir model, with the maximum adsorption amounts of Cu(II) and Zn(II) being 170.69 and 155.98 mg/g. Furthermore, competitive adsorption was observed among Fe (II), Cu (II), and Zn (II) in a multi-component system, with the adsorption priority being Fe (II) > Cu (II) > Zn (II). The removal mechanism of Fe(II), Cu(II), and Zn(II) in AMD by SS mainly includes electrostatic attraction, chemical precipitation, and surface complexation. Interestingly, the leached concentrations of Fe(II), Cu(II), and Zn(II) from the spent slag after calcination were all within the detection limit of the Chinese emission standard, demonstrating excellent environmental stability. Theoretically, this renders it a viable candidate for use as an additive in construction materials. Meaningfully, the work offers a practical approach for energy-efficient and eco-friendly heavy metal ions adsorption, and the secondary utilization of SS also contributes to the sustainable development of the steel industry. It is beneficial to implement the development concepts of clean production and efficient utilization of industrial solid waste.