Fe Values Research Articles

In situ activation of Sn(OH)4 catalyst for efficient CO2 electroreduction to formate

Electroreduction of CO2 into the highly valuable fuel formic acid (HCOOH) has been considered an ideal method for converting renewable energy and addressing environmental challenges. Herein, we present a straightforward and rapid method for preparing Sn(OH)4 catalysts specifically designed for electroreducing CO2 to formate. The Sn(OH)4 catalyst obtained through in-situ electrochemical reduction transforms from bulk morphology to nanoporous form, featuring numerous grain boundaries and a high hydroxyl content, enhancing its stability and availability of active sites.The resulting electrocatalyst demonstrates a remarkable formate faradaic efficiency (FEformate) exceeding 80 % across a broad potential range (−0.9 to −1.9 V). Notably, a peak FE value of 92 % is achieved for HCOOH production at −1.7 V vs RHE. This study presents a novel and effective method for developing high-performance Sn-based catalysts.

Effect of Poor Post-Slaughter Handling on Physicochemical and Microbial Quality of Fresh Broiler in Bangladesh

The slaughtering method and post-handling play an important role in meat processing. Countries followed different slaughtering methods, post-handling, and preservation techniques for post-slaughtered meat. Stress-oriented slaughtering, unhygienic handling, processing, and improper preservation are triggering factors of rapid oxidation and microbial proliferation in meat during storage. Bangladesh is a Muslim-oriented country but many vendors do not follow the halal slaughtering, and handling of meat in an unhygienic way due to a lack of food safety knowledge. Thus, the study aims to assess the effect of poor post-slaughtering handling practices on the physiochemical properties which include moisture, ash, protein content, fat content, drip loss, cooking loss, water holding capacity, pH, fat oxidation, color, heme iron, mineral content, and microbial qualities of fresh samples by total plate count during 0 days, 15 days and 30 days frozen storage at -18ºC. The live broiler was purchased randomly and slaughtered instantly from different slaughter shops in Jashore City, Bangladesh. The laboratory analysis was performed following the standard method of meat sample analysis. The outcome of this study revealed that heme iron content, minerals like Ca, Fe, Zn, and lightness values decreased significantly (p < 0.05) during 30 days of storage at -18 ºC. Post-handling had no significant effect (p > 0.05) on protein and ash content at 0 and 15 days of storage but slowly decreased with increasing storage time. The continuous increase in pH, cooking loss, and TBARS value indicate rises in lipid oxidation noticed in all samples, especially during 16-30 days of frozen storage (p < 0.05). The total viable count significantly raised (p < 0.05) and reached the highest value of 7.27 log10 CFU/g and 7.44 log10 CFU/g respectively after 15 days and 30 days of frozen storage compared to fresh condition. Bacteriologically meat samples were of very poor quality during storage compared to fresh ones.

Influence of an iron dextran injection in various diseases on hematological blood parameters, including serum ferritin, neonatal dairy calves

BackgroundFeeding milk substitutes with low iron content or whole milk without iron supplementation is considered a major factor in developing iron-deficiency anemia in neonatal dairy calves. Young calves are often supplemented with iron dextran injections on the first day of life to prevent anemia. However, the effects of preventive treatment and the presence of disease on serum iron (Fe) concentrations, serum ferritin levels, and hematological blood parameters during the early neonatal stages have not been examined in detail. Therefore, we examined and evaluated the effects of iron dextran injections and health status on the development of hematocrit (Ht), red blood cells (RBC), hemoglobin concentration (Hb), erythrocyte indices (mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration), Fe, and serum ferritin concentrations in dairy calves within the first 10 days of life. The suitability of serum ferritin as a reliable indicator of anemia in very young calves was evaluated by correlating ferritin concentrations with known laboratory diagnostic parameters of anemia.ResultsIron supplementation significantly increased Fe levels (P = 0.048) but did not affect serum ferritin levels in neonatal calves. Fe concentrations were significantly lower in diseased than healthy calves (P = 0.0417). Iron supplementation significantly affected the health status, as observed in Ht (Ptreat=0.0057; Phealth=0.0097), RBC (Ptreat=0.0342; Phealth=0.0243), and Hb (Ptreat=0.0170; Phealth=0.0168). Serum ferritin levels did not significantly correlate with Fe levels. Both groups showed marked differences in ferritin levels, with the highest levels measured on day 2. Fe concentrations showed weak negative correlations with Hb and Ht levels on day 3 (ρ=-0.45; P = 0.0034 and ρ=-0.045; P = 0.0032, respectively). RBC count showed strong positive correlations with Hb and Ht levels (ρ = 0.91 and ρ = 0.93; P < 0.001).ConclusionIron dextran injections increased Fe concentrations but reduced Ht level, RBC count, and Hb level. The presence of diseases led to a reduction in Fe and higher values of Ht, RBC, and Hb in moderate disease than in severe disease. Due to physiological fluctuations during the first 3 days of life, serum ferritin level seems unuseful for evaluating iron storage before day 4 of life.

Crystal growth and characterization of Fe1+δSe1-xTex (0.5 ≤ x ≤ 1) from LiCl/KCl flux

An eutectic LiCl/KCl flux method in a horizontal configuration has been used to grow a series of homogeneous Fe1+δSe1-xTex single crystals of high quality with 0.5 ≤ x ≤ 1. Compared with previously used melt-growth method, the stable crystallization process in LiCl/KCl flux below their peritectic temperatures results in better homogeneity and crystalline perfection identified by energy dispersive spectrometer and x-ray diffraction. The interstitial Fe value δ remains small within 0.5 ≤ x ≤ 0.85 where the superconducting temperature TC is not sensitive to the Te content with sharp superconducting transition widths ΔTC < 1 K and a maximum of TC = 14.3 K at x = 0.61. The value δ starts to increase quickly accompanied by a deviation of linear behavior of crystal lattice parameters as well as the broadening of ΔTC = 2.1 K at x = 0.91, then suddenly rises up to δ > 0.1 followed by the disappearance of superconductivity and emergence of antiferromagnetic order at x ≥ 0.96. We also observed a metallic to semiconducting transition in the normal state resistivity of Fe1+δSe1-xTex with increasing Te content which is related to a localized electronic state induced by the interstitial Fe. The interstitial Fe value δ might be a key physical parameter to understand various properties of Fe1+δSe1-xTex system.

Highly oxidized intraplate basalts and deep carbon storage.

Deep carbon cycle is crucial for mantle dynamics and maintaining Earth's habitability. Recycled carbonates are a strong oxidant in mantle carbon-iron redox reactions, leading to the formation of highly oxidized mantle domains and deep carbon storage. Here we report high Fe3+/∑Fe values in Cenozoic intraplate basalts from eastern China, which are correlated with geochemical and isotopic compositions that point to a common role of carbonated melt with recycled carbonate signatures. We propose that the source of these highly oxidized basalts has been oxidized by carbonated melts derived from the stagnant subducted slab in the mantle transition zone. Diamonds formed during the carbon-iron redox reaction were separated from the melt due to density differences. This would leave a large amount of carbon (about four times of preindustrial atmospheric carbon budget) stored in the deep mantle and isolated from global carbon cycle. As such, the amounts of subducted slabs stagnated at mantle transition zone can be an important factor regulating the climate.

Water-Insoluble Copper Complexes As Electrocatalysts for CO2 Reduction

The electrochemical reduction of carbon dioxide (CO2R) constitutes a promising CO2 utilization technology, allowing the production of valuable fuels and chemicals by using electrical energy from renewable sources. Nevertheless, poor selectivity and high required overpotentials hamper practical applications of the CO2R, which highlights the need for the development of more efficient electrocatalysts. Different copper-based materials have been extensively studied as electrocatalysts for CO2R. Particularly, copper complexes exhibited interesting properties under operational conditions: many of them undergo structural modifications (e.g. changes in oxidation state and/or coordination number), which potentially affect activity, selectivity and stability. Interestingly, some complexes exhibit reversible restructuring under specific conditions, which can be an interesting property to reach higher stability. In this presentation, we will show the results obtained for the electrocatalysis of water-insoluble copper complexes for the CO2R. The activity, selectivity and stability of both [Cu(bzimpy)Cl2] and [Cu(pyrben)2(NO3)]NO3 were investigated in K2SO4 0.1 mol L-1 (CO2 sat.) under different electrochemical conditions. Here, bzimpy and pyrben stand for 2,6-bis(2-benzimidazolyl)pyridine and 2-(2-pyridyl)benzimidazole, respectively. Qualitative EC-MS (Electrochemistry Coupled to Mass Spectrometry) analysis evidenced that both complexes are active for CO2 reduction and that product distribution changes according to the applied potential. Quantitative gas chromatography measurements revealed that, at -1.24 V vs. RHE, [Cu(bzimpy)Cl2] promotes the formation of H2, CO, CH4 and C2H4 with faradaic efficiencies of 26, 3.4, 9.2 and 31%, respectively. On the other hand, [Cu(pyrben)2(NO3)]NO3 shows FE values of 24, 8.8, 15 and 24% for H2, CO, CH4 and C2H4, respectively. After 1.6 h of electrolysis, the former exhibited stable current and FE of ~42% towards ethylene formation.

Evaluation of Oxidative Stress, Thyroid Hormones, Trace Elements and Some Biochemical Markers in Goats Naturally Infected with Theileria ovis.

Theileriosis is a tick-borne disease caused by protozoon species in the Theileria genus of the Theileriidae family. The biochemical changes induced by infection are considered to be an important understanding of the pathophysiology of caprine theileriosis. In this study, it was aimed to determine oxidative stress, thyroid hormones, trace elements, and biochemical parameters in theileriosis infection. A sample of 14 goat was used for this purpose, of which 7 were healthy and 7 were infected with Theileria ovis. Theileria infection was diagnosed from the polymerase chain reaction (PCR). Sera from blood samples was tested for total antioxidant capacity (TAC), total oxidant capacity (TOC), oxidative stress index (OSI), alanine aminotransferase (ALT), aspartate transaminase (AST), gamma glutamyl transferase (GGT), total protein, albumin, triglyceride, cholesterol, high density lipoprotein (HDL), low density lipoprotein (LDL), urea, blood urea nitrogen (BUN), creatinine, triiodothyronine (T3), thyroxine (T4), copper (Cu), zinc (Zn), cobalt (Co), manganese (Mn), selenium (Se), iron (Fe). TOC, OSI, AST, ALT and GGT values were higher in the patient group than in the healthy group (P < 0.05). On the other hand, there were decreases in TAC, T3, T4, total protein, albumin, creatinine, Cu, Zn, Se, and Co values (P < 0.05). However, there was not found to be a statistical difference between the healthy and patient groups in terms of triglyceride, cholesterol, HDL, LDL, urea, BUN, Mn, and Fe values (P > 0.05). It can be stated that oxidative stress is a complication of caprine theileriosis and it may be accompanied with hypothyroidism and deficits in trace minerals.

Stable production of hydrogen peroxide over zinc oxide @ zeolitic imidazolate Framework-8 composite catalysts

A promising method of producing hydrogen peroxide (H2O2) is the electrochemical two-electron water oxidation reaction (2e− WOR). In this process, it is important to design electrocatalysts that are both earth abundant and environmentally friendly, as well as offering high stability and production rates. The research of WOR catalysts, such as the extensively used transition metal oxides, is mainly focused on the modification of transition metal elements. Few studies pay attention to the protective heterostructure of metal oxides. Here, we demonstrate for the first time an organometallic skeleton protection strategy to develop highly stable WOR catalysts for H2O2 generation. Unlike the pure ZnO and zeolite imidazole framework-8 (ZIF-8) catalysts, ZnO@ZIF-8 enabled the production of hydrogen peroxide at high voltages. The experimental results demonstrate that the ZnO@ZIF-8 catalyst stably generates H2O2 even under a high voltage of 3.0 V vs. RHE, with a yield reaching 2845.819 μmolmin−1 g−1. ZnO@ZIF-8 shows a relatively low overpotential, with a current density of 10 mA cm−2 and an overpotential of 110 mV. The ZnO@ZIF-8 catalyst’s maximal FE value was 4.72 %. Moreover, the ZnO@ZIF-8 catalyst exhibits remarkable durability even after an extended 60-hour stability test. Operando Raman and theoretic calculation analyses reveal that the metal–organic skeleton being encapsulated on the metal oxide surface synergizes with each other, not only expanding the electrochemical surface area, but also adjusting the catalyst metal sites’ adsorption capacity. A novel approach to the modification of 2e− WOR metal oxide catalyst is presented in this work.

Machine learning-based prediction of cadmium pollution in topsoil and identification of critical driving factors in a mining area.

Mining activities have resulted in a substantial accumulation of cadmium (Cd) in agricultural soils, particularly in southern China. Long-term Cd exposure can cause plant growth inhibition and various diseases. Rapid identification of the extent of soil Cd pollution and its driving factors are essential for soil management and risk assessment. However, traditional geostatistical methods are difficult to simulate the complex nonlinear relationships between soil Cd and potential features. In this study, sequential extraction and hotspot analyses indicated that Cd accumulation increased significantly near mining sites and exhibited high mobility. The concentration of Cd was estimated using three machine learning models based on 3169 topsoil samples, seven quantitative variables (soil pH, Fe, Ca, Mn, TOC, Al/Si and ba value) and three quantitative variables (soil parent rock, terrain and soil type). The random forest model achieved marginally better performance than the other models, with an R2 of 0.78. Importance analysis revealed that soil pH and Ca and Mn contents were the most significant factors affecting Cd accumulation and migration. Conversely, due to the essence of controlling Cd migration being soil property, soil type, terrain, and soil parent materials had little impact on the spatial distribution of soil Cd under the influence of mining activities. Our results provide a better understanding of the geochemical behavior of soil Cd in mining areas, which could be helpful for environmental management departments in controlling the diffusion of Cd pollution and capturing key targets for soil remediation.

Genesis and Related Reservoir Development Model of Ordovician Dolomite in Shuntogol Area, Tarim Basin

The Ordovician thick dolostone in Shuntogol area of the Tarim Basin has the potential to form a large-scale reservoir, but its genesis and reservoir development model are still unclear. Starting from a sedimentary sequence, this study takes a batch of dolostone samples obtained from new drilling cores in recent years as the research object. On the basis of core observation and thin section identification, trace elements, cathodoluminescence, carbon and oxygen isotopes, rare earth elements, and X-ray diffraction order degree tests were carried out to discuss the origin of the dolomite and summarize the development model of the dolostone reservoir. The analysis results show that the Ordovician dolomite in the study area had a good crystalline shape, large thickness, high Fe and Mn values, and mostly showed bright red light or bright orange–red light under cathode rays. The ratio of δ18O values to seawater values at the same time showed a negative bias; the δCe values were negative anomalies, the δEu values were positive anomalies, and the order degree was high. This indicates that the dolomitization process occurred in a relatively closed diagenetic environment. The Ordovician carbonate rocks in the study area were low-lying during the sedimentary period, and with the rise of sea level, the open platform facies continued to develop. When the Middle and Lower Ordovician series entered the burial stage, the main hydrocarbon source rocks of the lower Cambrian Series entered the oil generation peak, and the resulting formation overpressure provided the dynamic source for the upward migration of the lower magnesium-rich fluid, and the dolomitization fluid entered the karst pore system in the target layer to produce all the dolomitization. This set of dolostone reservoirs is large in scale and can be used as a favorable substitute area for deep carbonate exploration for continuous study.

Ferric Iron in Eclogitic Garnet and Clinopyroxene from the V. Grib Kimberlite Pipe (NW Russia): Evidence of a Highly Oxidized Subducted Slab

Abstract Estimates of oxygen fugacity of eclogitic rocks are linked to the redox evolution of the oceanic protolith during subduction and its residence in the lithospheric mantle, and, based on knowledge of pressures and temperatures, allow modelling of the speciation of volatile elements and diamond (or graphite) versus carbonate stability. To date, the oxygen fugacity of mantle eclogites has been shown to vary between −6 (Kasai, Congo and Udachnaya, Siberia) and −0.1 (Udachnaya, Siberia) log units (relative to the fayalite–magnetite–quartz buffer, FMQ), linked to the low Fe3+ contents of garnets. In this study, we investigated the Fe oxidation state of coexisting garnet and clinopyroxene hand-picked out of 17 diamond-free high-MgO and low-MgO mantle eclogites (dated at 2.84 Ga) from the Grib kimberlite pipe (East-European platform). Measured Fe3+/∑Fe values range between 0.03 and 0.19 for garnet and 0.18–0.38 for clinopyroxene, the former being higher than what was measured previously in garnets equilibrated at mantle conditions. The Fe3+/∑Fe of the reconstructed bulk rock ranges between 0.10 and 0.15 for high-MgO eclogites and 0.10 and 0.24 for low-MgO eclogites (with uncertainties of ± 0.02 and ± 0.03 in both cases). Thermobarometric calculations result in equilibration pressures and temperatures of 3.0–5.2 (± 0.4) GPa and 720–1050 (± 60) °C for both high-MgO and low-MgO eclogites, slightly lower than previous P–T estimates of mantle eclogites from the Udachnaya kimberlite pipe (Siberian craton). At these conditions, ∆logfo2 (FMQ) calculated using the available oxythermobarometric model varies from −1.7 to −0.6 log units for high-MgO eclogites and from −2.9 to 0.9 log units for low-MgO eclogites. Samples recording ∆logfo2 (FMQ) ≤ −1 log units overlap with North Slave, West Africa and Udachnaya eclogites, with no difference among eclogite types. The average values of −1.2 (± 0.4) log units for high-MgO and −0.6 (± 1.1) log units for low-MgO eclogites suggest different redox conditions of basaltic protoliths during subduction worldwide. Previous geochemical studies on the same rock samples reported evidence of cryptic metasomatism in both garnet and clinopyroxene that we demonstrate being not recorded by their major elements, while modal metasomatism evidenced by the presence of phlogopite as a product of interaction with a kimberlitic melt only affects the MgO of the bulk rock. Therefore, we suggest that high Fe3+/∑Fe ratios for garnet (&amp;gt; 0.10) and for reconstructed bulk rocks in the case of both low-MgO and high-MgO samples cannot be due to metasomatic interaction with an oxidized fluid, but rather are the consequence of Fe3+ redistribution in an unusually oxidized mafic protolith upon metamorphism. Our results highlight the redox variability of eclogites of Archaean age at conditions more oxidized than present-day mid-ocean ridge basalts (MORBs) and imply an oxidizing nature of the convective mantle source where magma was formed with consequent speciation of C in the form of carbonate fluid explaining, therefore, the lack of eclogitic diamonds in V. Grib kimberlite pipe.

A Comparative Approach to Sustainable Fish Meal: Prussian carp meal (Carassius gibelio Bloch, 1782)

In the present study, the usability of Prussian carp (Carassius gibelio) meal (PCM) as an alternative animal protein source in fish feeds was investigated by comparing it with anchovy (Engraulis encrasicholus) and sprat (Sprattus sprattus) meals in terms of their biochemical, fatty acid, amino acid and element compositions. Prussian carp were obtained by fishing and made into a meal (PCM). Anchovy (AM), and sprat (SM) meals were purchased from a commercial company. The amino acid analysis results show that PCM's total, essential, and non-essential amino acid values were lower than that of AM and SM (P &amp;lt; 0.05). The polyunsaturated fatty acids (PUFA) and Omega-6 values of PCM were higher than AM and SM; and lower than saturated fatty acids (SFA), Omega-3, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), atherogenicity index (AI) values (P &amp;lt; 0.05). According to the element analysis, the P and Ca values of the PCM were higher than the AM and SM (P &amp;lt; 0.05), and the Na, K, Fe, Cu, Zn and Se values were lower. According to the results of the present study, PCM can be utilized in the feed industry to boost the sustainability of fish meals used in feed production, which in turn will reduce the foreign dependency on vegetable and fish meals, and lower feed costs.

Trace element concentrations and chemical zoning of spodumene from magmatic and hydrothermal origins

Spodumene is a major lithium ore mineral mined from granitic pegmatites and can crystallize (1) from magma, (2) from hydrothermal fluid in miarolitic cavities or fracture-filling units, or (3) as a product of petalite breakdown. Although spodumene’s purity influences the economic value of lithium ore, its trace-element geochemistry is not entirely understood. This study investigated 24 unaltered spodumene samples from 21 localities formed through each of these three modes of origin. The chemical zoning of each spodumene sample was characterized using cathodoluminescence (CL), micro-X-Ray fluorescence mapping (µXRF), and/or qualitative laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) line scans, whereas the concentrations of trace elements were quantified using LA-ICP-MS point analyses. Intra-crystalline chemical zoning was present in all three spodumene types as either oscillatory growth bands and/or sector zoning. For the four most abundant transition and post-transition metals analyzed (Fe, Mn, Ga, Sn), the concentrations ranged from below detection to 10510 ppm (Fe), 1850 ppm (Mn), 300 ppm (Ga), 320 ppm (Sn), whereas Rb and Cs were below detection. Magmatic spodumene had the highest mean concentrations of Fe (2345 ppm) and Sn (94 ppm), hydrothermal spodumene had the highest mean concentrations of Mn (641 ppm) and Ga (94 ppm), and spodumene formed from the breakdown of petalite consistently had the lowest mean concentrations, though there was significant overlap in the datasets. In addition, texturally similar spodumene-quartz intergrowths of primary and secondary origins were distinguished via trace-element geochemistry. Principle component analysis of Fe, Mn, Ga, Sn, Ti, and Zn values from all 325 LA-ICP-MS measurements showed discrimination by CL color, as well as color in handsample for gem-varieties of hydrothermal spodumene.

Comparative study on the quality of wild and ecologically farmed large yellow croaker through on-site synchronous sampling from the Nanji Archipelago in the East China Sea

With consumers demanding higher quality in fish products, ecologically farmed fish are increasingly favored due to their quality being close to that of wild fish. However, the differences between the ecologically farmed and wild fish remain largely unclear. In the present study, the wild and ecologically farmed large yellow croakers of the same size were captured simultaneously from the same marine area around Nanji islands (27.479°E, 121.052°N). Then, synchronous tests were conducted to evaluate quality to clarify the key quality parameters that differentiate between the wild and farmed fish. We obtained 49 quality parameters after orthogonal partial least squares discriminant analysis (OPLS-DA) with variable importance in projection (VIP) scores >1 and p < 0.05 using 307 indicators related to 121 length ratios, 4 body color indicators, 5 muscle fiber characteristic indicators, 87 nutrition quality parameters, 40 taste parameters, and 50 volatile compounds. Compared to the farmed fish, the wild fish exhibited a more yellow skin color, higher levels of carotenoids, and a more streamlined conical shape. Changes in histology and ultrastructure of muscle fibers were noted, including increased muscle fiber density and the ratio of fiber area to gap, as well as reduced I band width, observed in the wild fish. The wild fish had high nutritional value of fatty acids and minerals and low nutritional value of amino acids, as reflected by higher levels of C22: 6n3 (DHA), Σn-3 PUFA (polyunsaturated fatty acids), Σn-3/Σn-6 PUFA, Na (sodium), K (potassium), Fe (iron), and Se (selenium), and lower values of ΣMUFA (monosaturated fatty acids), Σn-6 PUFA, TI (thrombogenic index), amino acid and chemistry scores of isoleucine, ΣEAA/ΣTAA (essential amino acid/ total amino acid), and ΣTAA/ΣNEAA (total amino acid/non-essential amino acid) in the muscles of the wild fish. The wild fish muscle showed high levels of hydrolyzed glycine and proline and free methionine, and low levels of free glycine and proline, indicating a propensity for collagen synthesis. Despite significant differences in the contents of fourteen flavor substances of free amino acids, 5′-nucleotides, and volatile compounds, their concentrations were notably below the corresponding threshold and contributed minimally to flavor, suggesting that the wild and farmed fish shared similar flavor characteristics. In summary, this study reveals the quality differences between ecologically farmed and wild large yellow croaker based on on-site synchronous sampling, providing a theoretical foundation for further enhancing the quality of this species.

Genealogical structure and genetic variability: A step towards conservation of white Morada Nova sheep in semi-arid region

Morada Nova breed has a low effective herd, and its white variety is in risk of extinction in Brazilian semi-arid region. This study aimed to evaluate white Morada Nova sheep’s genetic variability and population structure in four flocks. These are the only flocks in the world. The assessed parameters of pedigree integrity and a genealogy record of 219 animals. 44.74 % did not have pedigree information on their mother or father, and 50.47 % did not have available information on their grandparents. 52.97 % had a pedigree in their first ancestry (obtained through the average of known parents), 23.74 % in the second, 13.58 % in the third, and 5.33 % in the fourth. The effective size was 10.7, considering the complete equivalent generation. The effective number of founding animals (fe) and ancestors (fa) was 10, indicating the effective participation of all founding animals in the population over the generations, reducing losses of genetic variability. Out of all the ancestors, only 3 explained 50 % of the population’s genetic variability, reflecting the low values of fa and fe. The population’s average inbreeding and kinship coefficients were 2.61 and 4.54. The F statistics of Wright, Fis, Fst, and Fit, were −0.012, 0.016, and 0.003. The genetic conservation index (GCI) had an average of 2.01 ± 1.29, with minimum and maximum values of 1.0 and 6.38, respectively. Approximately, 71 % of the population had GCI below 2.0, while only 5.9 % of sheep had an GCI bigger than 5.0. This indicates the absence of sub-structures inf the population. There is no population subdivision, considering the genealogical structure of the evaluated flocks. The inbreeding and kinship coefficient values are controlled and serve as a starting point for establishing a future management plan for the genetic variability of the flock. It is recommended to use strategies to increase the effective population size, to meet the minimum number recommended by FAO and to promote the conservation and genetic improvement of the breed.

Elucidation of heavy metal content, phenolic profiles, and antioxidant activities of kale (Brassica oleracea L. var. acephala) and arugula (Brassica eruca L.) grown in urban gardens in Istanbul.

This study was conducted to evaluate the effect of two distances: close (0-10m) and far (60m) from the heavy traffic roadside, at three different cultivation sites (MS: Mevlanakapi-Silivrikapi, SB: Silivrikapi-Belgradkapi, and BY: Belgradkapi-Yedikule kapi) along the road line. First, the phenolic compounds, antioxidant activity, and physicochemical properties in kale and arugula vegetables were examined. Second, heavy metal concentrations in vegetables, soil, and irrigated water were investigated. In both vegetables, the highest total phenolic content was detected in samples obtained from far distance in SB site (3880.3mg/kg) for kale and in BY site (1459.9mg/kg) for arugula, whereas the lowest content was found at the close distance in MS site for both kale (448.5mg/kg) and arugula (586.4mg/kg). The antioxidant activity values [mg Trolox/kg (dw)] ranged from 366.74 to 586.10 and 2349.00 to 3757.4 for kale and from 520.00 to 945.60 and 3323.00 to 5814.70 for arugula in 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) and 2,2-diphenyl-1-picrylhydrazyl methods, respectively. The levels of Cd and Hg in kale and arugula and Fe content in arugula exceeded FAO/WHO permissible limits, making them unsafe for human consumption. Meanwhile, the Pb content in kale and arugula and Fe content in kale were observed to be within acceptable limits set by FAO/WHO. In the irrigated water, the Pb value was below the permissible limit, whereas the Cd value was above it and no Hg and Fe were detected. In the soil samples, the Pb and Fe values were below the limit, whereas the Cd and Hg values were higher.

Geochronology and geochemistry of zircon and columbite–tantalite group minerals from the Weilasituo Sn–polymetallic deposit, northeastern China: Implications for the relationship between mineralization and the magmatic–hydrothermal transition

The Weilasituo Sn–polymetallic deposit, located in the southern portion of the Great Xing'an Range of Inner Mongolia, China, is a super-large Sn deposit associated with abundant Li, Rb, Nb, Ta, Zn, and Cu resources. Despite that previous studies have characterized the age, hydrothermal evolution, and genetic relationship between the alkali feldspar granite porphyry and associated Sn–polymetallic mineralization, the magmatic–hydrothermal evolution and ore–forming processes remain ambiguous. To address these ambiguities and bridge this knowledge gap, this contribution characterizes the texture, geochemistry, and U–Pb isotope composition of zircon and columbite–tantalite group minerals (CGMs) from amazonitized alkali feldspar granite (AMG) and albitized alkali feldspar granite (ABG) in the Weilasituo deposit. Type-I zircon (Zr1) is inclusion-poor, translucent, and is characterized by low light rare earth element (LREE) contents, high (Sm/La)N ratios (mean = 655.7), and low Th/U (mean = 0.21 < 0.3), Zr/Hf (mean = 5.46), and Y/Ho ratios (mean = 4.42), indicating that it formed during the magmatic–hydrothermal transition. Type-II zircon (Zr2) is inclusion-rich, porous, has a low CL response, and is characterized by low Th/U ratios (0.08–0.32, mean = 0.17), high LREE contents, weakly positive Ce anomalies, and low (Sm/La)N ratios (mean = 20.7), indicating that it formed via hydrothermal alteration of Zr1 (i.e., magmatic–hydrothermal zircon). Type-I CGM (CGM1) generally lacks oscillatory zoning, and has similar and positively correlated Ta/(Nb + Ta) and Mn/(Mn + Fe) values (AMG: R2 = 0.93; ABG: R2 = 0.75), indicative of a magmatic origin. Type-II CGMs (CGM2) occur as rims on CGM1 and are characterized by higher Ta/(Nb + Ta) and lower Nb/Ta ratios than CGM1, indicative of precipitation from a hydrosilicate liquid during the magmatic–hydrothermal transition. Based on the characteristics of CGMs, two stages are evident in the evolution of the Weilasituo granite porphyry: an earlier magmatic differentiation stage and a later magmatic–hydrothermal transition stage. Furthermore, the magmatic–hydrothermal transition stage can be subdivided into the AMG and ABG substages within the porphyry system based on petrological and mineralogical characteristics. The U–Pb ages for zircons and CGMs from the alkali feldspar granite porphyry range from 137.2 ± 2.0 Ma to 129.8 ± 1.4 Ma, without a notable age gap. The similarity in U–Pb ages between CGM1–CGM2 and Zr1–Zr2 indicates that the magmatic stage and the magmatic–hydrothermal transition at Weilasituo were continuous processes that occurred during the Early Cretaceous.

Non-carcinogenic risk assessment and sources apportionment of heavy metals in pomegranate in Anhui, China

This study examined the concentrations, sources, and health risks associated with 7 heavy metals in Chinese pomegranates. The results showed that the heavy metal in pomegranates was within standard limits, and the accumulation of heavy metals was low. PCA showed that Cd and Hg in pomegranates originate from irrigation water, Zn, As, and Cu from soil, and Cr and Pb from fertilizers. MLR and Monte Carlo sensitivity analysis showed that soil and irrigation water were the primary sources of heavy metals in pomegranates, with Zn, As, Cu, and Pb primarily originating from soil, and Cd, Cr, and Pb predominantly coming from irrigation water. The presence of organic matter and Ca in soil influenced heavy metal accumulation in pomegranates, other properties (Mg, Fe, and pH value in soil) have minor effects. The TTHQ for both adults and children remained below 1, while the TTRisk exceeded 1×10−4, mainly due to the hazardous impact of As in water. The upper 95% uncertainty limit indicated that residents were exposed to both non-carcinogenic and carcinogenic risks, primarily due to the toxicity of Cr in soil and As in water. Strengthening heavy metal screening in soil and water and enhancing pollution management policies are imperative.

Geochemical characteristic and B isotopic compositions of tourmaline from the Chaqiabeishan Li-rich pegmatite in the Quanji Massif, NW China

The Chaqiabeishan Li-rich pegmatite deposit is located in Tianjun County, Qinghai Province. Due to the complex magmatic evolution, there are still numerous controversies surrounding the diagenetic and metallogenic mechanisms of pegmatites. In this study, we investigated tourmalines from pegmatites in Chaqiabeishan by means of analyzing the in situ major element compositions, trace element contents, and boron isotopes. The collected samples can be classified into two types: pegmatitic tourmaline (Tur 1) and fine tourmaline (Tur 2). Based on the observation of geological characteristics, specimens, and microphotographs, the tourmalines have a basically paragenetic relationship with the predominant lithium-bearing mineral (spodumene), tourmalines and spodumenes would crystallize at a late magmatic stage of the pegmatitic sequence. Both tourmalines have similar geochemical characteristics, and Tur 1 crystallized earlier than Tur 2. The major elements show that both tourmalines belong to the alkali group, schorl series, and Li-poor pegmatite. Additionally, they have ∑(Mg + Fe) values less than 3 apfu, and redundant Al (0.04–0.89 apfu, average of 0.61) in the Y-site occupancy. The trace elements show that both tourmalines are characterized by enrichment in LREE relative to the MREE, with a slight negative Eu anomaly, indicating that they are of magmatic origin. The high Li/Sr ratios ranging from 38.56 to 6292.28 (average of 701.01 ppm) further support the magmatic origin. The δ11B values of all tourmalines range from −13.86 to −12.46 ‰, with an average of −13.14 ‰, indicating that the boron in the pegmatites was derived from S-type granitic magma or Dakendaban Group mica schist basement. The δ11B values of Tur 1 (average of −13.13 ‰), the rim of Tur 1 (average of −12.95 ‰), the core of Tur 1 (average of −13.25 ‰), and Tur 2 (average of −13.19 ‰) show a slight variation, indicating that the tourmalines have a consistent boron source and basically no foreign B-rich fluids involved. In conclusion, the petrological and geochemical characteristics suggest that the pegmatites in Caqiabeishan are likely the direct products of anatexis, and the tourmalines and spodumenes were formed in secondary faults at the late magmatic stage.

Hazardous impacts of heavy metal pollution on biometric and biochemical composition of pearl oyster Pinctada radiata from five sites along Alexandria coast, with reference to its potential health risk assessment

This study investigated the effect of heavy metals on the pearl oyster Pinctada radiata from 5 sites along the coast of Alexandria, with focus on its ecological health and potential risks to human consumption. Pollution results showed that Abu-Qir had the highest Cu and Cd values. Montaza and Eastern Harbor had the highest Fe and Pb values, respectively. Statistically, differences in metal concentrations among study sites were significant (p < 0.05). Non-carcinogenic risk (TTHQ) of tested metals and carcinogenic ones of Cd and Pb showed “high risk” on human health by consuming pearl oysters. Morphometric measurements and condition indices were studied to assess growth patterns and health in relation to heavy metals exposure. Key findings showed detectable declines in size and condition index in Eastern Harbor, whereas Abu-Qir recorded the highest values. This condition index performance presented Abu-Qir, Mammora, and Miami as ideal locations for spat collection and oyster rearing, potentially enhancing Egyptian pearl farming. Average values of spatial proximate contents of pearl oyster showed that it was rich in proteins (33.07–58.52%) with low fat content (1.39–1.87%) and carbohydrates (9.72–17.63%). Biochemical composition of pearl oyster demonstrated its high nutritional value which supported its promotion as a functional food for human consumption. The calorie content of pearl oyster was less than 2 Kcal, making this species an alternative source of healthy food to reduce obesity. Regression analysis indicated that Cu, Cd, and Pb had significant effect on 2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity, calories, vitamins, and pigment content of the collected oysters.