Inorganic Constituents Research Articles

Chemical Fingerprinting of PM2.5 via Sequential Speciation Analysis Using Electrochemical Mass Spectrometry.

Chemical fingerprinting to characterize the occurrence state and abundance of organic and inorganic constituents within fine particulate matter (PM2.5) is useful in evaluating the associated health risks and tracing pollution sources. Herein, an analytical strategy for the rapid analysis of metal and organic constituents in PM2.5 was developed employing a combination of sequential chemical extraction coupled with mass spectrometry detection. H2O, CH3OH, EDTA-2Na, electrochemical oxidation, and electrochemical reduction were sequentially utilized to extract the chemical constituents in PM2.5 samples on a homemade device employing simultaneous online detection using two linear trap quadrupole mass spectrometers (LTQ-MS) with electrospray ionization (ESI) in positive and negative modes. After a single analytical procedure, dozens of metals (e.g., Pb, Cr, and Cu), organic compounds (e.g., amines, polycyclic aromatic hydrocarbons, and aliphatic acids), and negative ions (e.g., NO3-, NO2-, and Cl-) were comprehensively detected in the water-soluble, liposoluble, insoluble, oxidizable, and reducible fractions of PM2.5 samples, and their physical and chemical relationships were established.

Applications of hydroxyapatite-based polymeric scaffolds in bone tissue engineering: An update

Bone tissue is a comprising of an organic and inorganic environment, in which the collagen element and the mineral part are structured into complex and spongy constructions. Hydroxyapatite (HAp) is the chief inorganic constituent of human bone. HAp is extensively utilized in bone tissue regeneration for its bioactivity and biocompatibility, and a rising number of investigators are discovering ways to recover the physical belongings and biological roles of HAp. However, this biomimetic material has poor mechanical properties, such as low tensile and compressive strength, which make it not suitable for bone tissue engineering (BTE). For this reason, HA is frequently utilized in a mixture with diverse polymers to increase their mechanical strengths and the general performance of the implantable biomaterials advanced for orthopedic usage. In this review, we attempt to contribute a brief and inclusive outline of HAp-based natural and synthetic polymer materials as reinforcing components and their applications in bone tissue engineering.

Niger Delta Oilfields Produced Water Characteristics and Treatment Technologies: Challenges and Solutions

The Nigerian Niger Delta oilfields have high water-to-oil ratio ranging from 50% to 95% water content, due to its secondary and tertiary production phases. Oil and gas producers could shut-in such wells, or develop cost effective approach for Produced Water, PW handling to meet reinjection or environmental permissibility. Thus, the study investigated the compositions and treatment techniques of Niger Delta oil and gas fields PW, and proffered solutions for actualizing minimal hazardous contaminants in PW. Characterization of PW from a Flow Station, an Oil processing and a Gas processing facilities showed biogeochemical homogeneity in the PW compositions with high organic and inorganic constituents, which are above injection and disposal specifications. The results of treated PW from the extant PW treatment (PWT) techniques showed that the total dissolved solids (TDS) concentration (6105.9 mg/l) from the Flow Station PW treatment facility did not meet the required specifications for injection into depleted wells or disposal into the environment (2,000.00 mg/l for inland, and 5,000.00 mg/l for nearshore). The salinity contents in the treated PW from the three PWT configurations were 2411.0 mg/l, 2218.6 mg/l, and 2165.4 mg/l, respectively, which were slightly above Nigerian Upstream Petroleum Regulatory Commission (NUPRC) specification (2000.0 mg/l) for nearshore disposal. The chemical oxygen demand (COD) concentration in the treated PW from the three PWT configurations were 153.0 mg/l, 148.1 mg/l, and 141.2 mg/l, respectively, which were above the NUPRC standard (125.0 mg/l). The oil and grease (O&G) concentration in the treated PW were 84.7 mg/l, 51.5 mg/l, and 58.0 mg/l, respectively, which also were above regulatory stipulation (30.0 mg/l) for nearshore disposal. The modular Bio-Unit + Ultra/Nanofiltration achieved more than 95% removal of both organic and inorganic constituents in the PW. Therefore, this study suggests that reconfiguring the extant PW treatment equipment with this cost-effective innovation would be the solution to PW treatment challenges in the Niger Delta oil and gas operations.

Chemical speciation and oxidative potential of PM10 in different residential microenvironments: Bedroom, living room and kitchen

Exposure to particulate matter (PM) and its chemical constituents in residential microenvironments has become a major health concern worldwide. The oxidative potential (OP) has been proposed as a metric for estimating the PM capacity to induce oxidative stress and, consequently, health effects. In the present study, PM10 was daily monitored simultaneously in the bedroom, living room and kitchen of three dwellings for one week in a small town of Portugal, to perform a detailed characterisation of its organic and inorganic constituents and the determination of the OP. Bedrooms (B) were found to be a hotspot of PM10 concentrations (B1 = 22.7 μg m−3; B2 = 19.5 μg m−3; B3 = 68.1 μg m−3). PM10-bound elements varied significantly between microenvironments in all dwellings. Lower molecular weight polycyclic aromatic hydrocarbons (PAHs) were found to be between 14 and 72 times higher than high molecular weight PAHs in bedrooms. The mean volume-normalised OP determined by the dithiothreitol and ascorbic acid assays varied within the 0.01–0.38 nmol min−1 m−3 and 0.03–0.53 nmol min−1 m−3 ranges, respectively. Quinones, oxy-aromatic, aromatic and alkyl-aromatic compounds stood out in bedrooms. Strong and significantly positive relationship between OP and black carbon, Cu and Br were observed, indicating common redox active species mainly associated with traffic emissions. Sr, Fe, Zn and Zr presented higher concentrations in dwelling 3, exhibiting excellent positive correlation with OP, indicating that the Sahara dust intrusion recorded in that house may have contributed to the formation of more redox active species thought to drive antioxidant depletion responses.

Investigations on performance of gasifier engine integration using three different biomasses as feedstocks

The integration of a downdraft gasifier with modified internal combustion engines presents a feasible solution for heat and power production, such as off-grid areas. This study conducted an experimental analysis to evaluate combustion in a modified engine. The morphological characteristics of the agricultural residue used in the gasifier were analyzed using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy (SEM), along with an examination of the slagging inorganic constituents. The engine used in the experiments was a modified single-cylinder design paired with a downdraft gasifier. Three types of biomass feedstocks—eucalyptus, corncob, and pearl millet in pellet form —were tested. The performance of the downdraft gasifier was stabilized, and the engine was run independently on each type of producer gas at a constant speed under different loads to determine the optimum load. Cylinder pressure measurements were taken to estimate the heat release rate.The study found that power generation was lower than typical woody biomasses due to the lower calorific value of the producer gas from the tested feedstocks. Additionally, lower cylinder pressures and heat release rates were recorded, along with longer combustion durations. The varying proportions of producer gas affected combustion stability. Among the studied ashes, pearl millet corncob (PMC) exhibited the highest slagging tendency, followed by corncob (CC). Morphological analysis indicated that the eucalyptus residue's increased porosity was caused by the volatiles changing, forming pores and tube-like structures. An aliphatic C–H peak (3000–2500 cm⁻1) is absent from the residue, indicating that the aliphatic structure was disturbed during thermochemical conversion. During the gasification process, the residue's crystallinity reduced as it split down.

Authentication of edible herbal materials and food products using mass spectrometry based metabolites and inorganic constituents

Medicinal food homologous (MFH) substances not only provide nutrition but also serve as a traditional means to overcome many health issues. Authentication of these products verifies their efficacity and assures consumers of a genuine product. In this review paper, we focus the determination of MFH authenticity including geographical identification and adulteration detection using mass spectrometry (liquid and gas chromatography) based metabolites and inorganic constituents (muti-elements and stable isotopes). The application of these techniques to determine product identification characteristics combined with chemometrics are discussed, along with the limitations of these techniques. Multi-elements, stable isotopes, and metabolite analysis are shown to provide an effective combination of techniques to resolve the origin of various MFH products. Most organic compounds from MFH products are identified using chromatographic separation techniques (HPLC, GC) combined with different detection methods. Chemometric analysis of organic and inorganic fingerprints offers a robust method to detect and classify mislabeled and suspected fraudulent samples of different MFH products.

Mixed contaminant exposure in tapwater and the potential implications for human-health in disadvantaged communities in California

Water is an increasingly precious resource in California as years of drought, climate change, pollution, as well as an expanding population have all stressed the state's drinking water supplies. Currently, there are increasing concerns about whether regulated and unregulated contaminants in drinking water are linked to a variety of human-health outcomes particularly in socially disadvantaged communities with a history of health risks. To begin to address this data gap by broadly assessing contaminant mixture exposures, the current study was designed to collect tapwater samples from communities in Gold Country, the San Francisco Bay Area, two regions of the Central Valley (Merced/Fresno and Kern counties), and southeast Los Angeles for 251 organic chemicals and 32 inorganic constituents. Sampling prioritized low-income areas with suspected water quality challenges and elevated breast cancer rates. Results indicated that mixtures of regulated and unregulated contaminants were observed frequently in tapwater throughout the areas studied and the types and concentrations of detected contaminants varied by region, drinking-water source, and size of the public water system. Multiple exceedances of enforceable maximum contaminant level(s) (MCL), non-enforceable MCL goal(s) (MCLG), and other health advisories combined with frequent exceedances of benchmark-based hazard indices were also observed in samples collected in all five of the study regions. Given the current focus on improving water quality in socially disadvantaged communities, our study highlights the importance of assessing mixed-contaminant exposures in drinking water at the point of consumption to adequately address human-health concerns (e.g., breast cancer risk). Data from this pilot study provide a foundation for future studies across a greater number of communities in California to assess potential linkages between breast cancer rates and tapwater contaminants.

Elevated effect of hydrothermal treatment on phosphorus transition between solid-liquid phase in swine manure

The morphology and composition of phosphorus in biomass wastes are key factors in determining its potential for utilization. However, the morphological distribution and evolutionary mechanism of phosphorus during the hydrothermal conversion of biomass wastes are still unclear. In this study, swine manure was investigated as the research subject, and the changes in its solid-phase organic components, such as lignocellulose, and inorganic constituents, including metals and phosphorus, during the hydrothermal carbonization (HTC) processes were analyzed in relation to hydrothermal reaction severity (LnR0). A significant linear correlation in Phase II was observed between the solid-phase yield of swine manure and the LnR0. The rapid decline in the solid-phase yield during the initial phase (LnR0 < 9.72) was primarily attributed to the hydrolysis of hemicellulose and similar components. Similarly, solid phase phosphorus showed a very significant phase II with the decrease of solid phase yield. In the first stage, inorganic phosphorus and metal ions (calcium ions, magnesium ions) transferred to the liquid phase (LnR0<9.41). When LnR0 > 9.41, and the driving force of inorganic phosphorus and metal ions into solid phase is enhanced. As the LnR0 was further increased, the HTC could fix over 90 % of the total phosphorus content. XANES analysis indicated that hydroxyapatite emerged as the predominant phosphorus fraction in the solid-phase products, comprising more than 60 %, while magnesium ammonium phosphate components also appeared. This research elucidates the underlying mechanisms of component interaction and phosphorus transformation, providing a solid foundation for enhancing the reuse efficiency of phosphorus in wastes.

In Situ Inorganic/Organic Protective Layer on Carbon Paper as Advanced Current Collector for Robust Li Metal Anode.

Lithium (Li) metal is regarded as the most promising anode for next-generation batteries with high energy density. However, the uncontrolled dendrite growth and infinite volume expansion during cycling seriously hinder the application of Li metal batteries (LMBs). Herein, an inorganic/organic protective layer (labeled as BPH), composed of in situ formed inorganic constituents and PVDF-HFP, is designed on the 3D carbon paper (CP) surface by hot-dipping method. The BPH layer can effectively improve the mechanical strength and ionic conductivity of the SEI layer, which is beneficial to expedite the Li-ion transfer of the entire framework and achieve stable Li plating/stripping behavior. As a result, the modified 3D CP (BPH-CP) exhibits an ultrahigh average Coulombic efficiency (CE) of ≈99.7% over 400 cycles. Further, the Li||LiFePO4 (LFP) cell exhibits an extremely long-term cycle life of over 3000 cycles at 5 C. Importantly, the full cell with high mass loading LiFePO4 (20mgcm-2) or LiNi0.8Co0.1Mn0.1O2 (NCM, 16mgcm-2) cathode exhibits stable cycling for 100 or 150 cycles at 0.5 C with high-capacity retention of 86.5% or 82.0% even at extremely low N/P ratio of 0.88 or 0.94. believe that this work enlightens a simple and effective strategy for the application of high-energy-density and high-rate-C LMBs.

Effect of HTC and Water-Leaching of Low-Grade Biomasses on the Release Behavior of Inorganic Constituents in a Calcium Looping Gasification Process at 650 °C.

The release of alkali metals (K, Na) and nonmetals (S, Cl) during a calcium looping (CaL) gasification process of waste derived-hydrochars, water-leached samples, and CaO-biomass blends was investigated. Special attention was paid to biomasses that are not particularly promising for gasification requirements but have a large occurrence in Europe, including Grape Bagasse, Organic Fraction of Municipal Solid Waste (OFMSW), Green Waste, and Out-of-use woods from construction debris and discarded furniture. The release experiments were performed at 650 °C in a flow channel reactor to investigate the behavior of inorganic trace substances. Hot-gas analysis was performed by Molecular Beam Mass Spectrometry (MBMS). Thermodynamic equilibrium calculations via FactSage indicate H2S, carbonyl sulfide (COS), KCl, NaCl, and HCl as the main inorganic impurities. Thus, the focus of the experiments was placed on these species. It was found that the concentrations of trace elements released during gasification at 650 °C, such as H2S, SO2, KCl, and NaCl, are hardly affected by intense water-leaching. In contrast, carbonaceous materials from hydrothermal carbonization exhibit a higher concentration of trace potassium substances (K, KCl, and K2Cl+). When biomass samples are combined with CaO, the total amount of inorganic trace compounds (K, Na, and S compounds) in the resulting syngas could be decreased.

Understanding Partial Denitrification-hydroxyapatite (PD-HAP) coupled granules to enhance process stability and phosphorus removal by investigating the size effect of granules

The innovative Partial Denitrification-hydroxyapatite (PD-HAP) coupled granule offers a promising biotechnology for supplying nitrite to Anammox while simultaneously removing phosphorus. This study systematically examined the characteristics, biomass activity, and microbial community of PD-HAP granules of various sizes to enhance system stability and phosphorus removal efficiency. The results showed that larger granules had higher inorganic mineral and extracellular polymeric substances (EPS) content. These factors contributed to their denser structure, smoother surfaces, and better settling velocities compared to smaller granules. In contrast, smaller granules exhibited higher denitrification activity due to their greater biomass content and more efficient mass transfer. Calcium and phosphorus were identified as the primary inorganic constituents, mainly in the form of HAP, and were especially abundant in larger granules. Granules larger than 3.0 mm demonstrated a higher capacity for phosphorus removal. This was due to their significantly greater tightly bound EPS (T-EPS) content, which led to increased HAP and phosphorus levels. All granule sizes maintained a nitrate-to-nitrite transformation ratio (NTR) above 80 %, primarily due to the dominance of Flavobacterium (65.8 %-74.9 %). Although larger granules had lower denitrification activity, they still achieved an excellent NTR (above 85 %). They also showed superior settling velocity (174.9 m/h) and stronger phosphorus removal capacity (54.1 mg/g SS) compared to smaller granules. Maintaining a dominant proportion of granules larger than 3.0 mm could be an effective strategy to enhance both system stability and phosphorus removal. This study provides valuable insights into the PD-HAP coupled granular process, promoting efficient nitrite production and effective phosphorus removal.

Effect of pH on hydroxyapatite coatings obtained by spray pyrolysis and their use as matrices for antibiotic adsorption by spin coating and release properties.

Calcium phosphate materials, particularly hydroxyapatite (HA), are extensively used in biomedical applications because of their prominence as primary inorganic constituents of human hard tissues. This study investigates the synthesis of HA coatings via spray pyrolysis using various precursors, including HA derived from bovine bone. The effects of pH on the formation and properties of HA coatings were systematically examined. Samples exposed to acidic conditions or left without pH adjustment led to the formation of HA, contrasting with the outcomes observed through dissolution methods. Different characterization techniques, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD), were employed to evaluate the quality and crystallinity of the coatings. Among the samples, those exhibiting superior crystallinity and nanostructured features, including bovine HA, were selected for further surface functionalization with the antibiotic enrofloxacin using spin coating. As expected, the antibiotic loading on each material's surface depended on the amount of HA deposited on the substrate. However, the desorption results indicated that, in all cases, desorption persisted beyond 38 h, implying that HA-loaded matrices could be effective systems for controlled and prolonged drug release, which could be useful in dental or orthopedic implants for inhibiting the growth of bacterial biofilms.

Vapor Growth of All-Inorganic 2D Ruddlesden-Popper Lead- and Tin-Based Perovskites.

The 2D Ruddlesden-Popper (RP) perovskites Cs2PbI2Cl2 (Pb-based, n = 1) and Cs2SnI2Cl2 (Sn-based, n = 1) stand out as unique and rare instances of entirely inorganic constituents within the more expansive category of organic/inorganic 2D perovskites. These materials have recently garnered significant attention for their strong UV-light responsiveness, exceptional thermal stability, and theoretically predicted ultrahigh carrier mobility. In this study, we synthesized Pb and Sn-based n = 1 2D RP perovskite films covering millimeter-scale areas for the first time, utilizing a one-step chemical vapor deposition (CVD) method under atmospheric conditions. These films feature perovskite layers oriented horizontally relative to the substrate. Multilayered Cs3Pb2I3Cl4 (Pb-based, n = 2) and Cs3Sn2I3Cl4 (Sn-based, n = 2) films were also obtained for the first time, and their crystallographic structures were refined by combining X-ray diffraction (XRD) and density functional theory (DFT) calculations. DFT calculations and experimental optical spectroscopy support band-gap energy shifts related to the perovskite layer thickness. We demonstrate bias-free photodetectors using the Sn-based, n = 1 perovskite with reproducible photocurrent and a fast 84 ms response time. The present work not only demonstrates the growth of high-quality all-inorganic multilayered 2D perovskites via the CVD method but also suggests their potential as promising candidates for future optoelectronic applications.

Inorganic Characterization of Feeds Based on Processed Animal Protein Feeds.

The potential of utilizing inorganic constituents in processed animal proteins (PAPs) for species identification in animal feeds was investigated, with the aim of using these constituents to ensure the quality and authenticity of the products. This study aimed to quantify the inorganic content across various PAP species and assess whether inorganic analysis could effectively differentiate between PAP species, ultimately aiding in the identification of PAP fractions in animal feeds. Four types of PAPs, namely bovine, swine, poultry, and fish-based, were analyzed and compared to others made up of feathers of vegetal-based feed. Also, three insect-based PAPs (Cricket, Silkworm, Flour Moth) were considered in this study to evaluate the differences in terms of the nutrients present in this type of feed. Ionic chromatography (IC) was used to reveal the concentrations of NO3-, NO2, Cl-, and SO42-, and inductively coupled plasma optical emission spectroscopy (ICP-OES) to detect Al, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, Ni, P, Si, Sr, Ti, and Zn. The application of multivariate chemometric techniques to the experimental results allowed us to determine the identification capability of the inorganic composition to identify correlations among the variables and to reveal similarities and differences among the different species. The results show the possibility of using this component for discriminating between different PAPS; in particular, fish PAPs are high in Cd, Sr, Na, and Mg content; swine PAPs have lower metal content due to high fat; feathers and vegetal feed have similar Al, Si, and Ni, but feathers are higher in Fe and Zn; and insect PATs have nutrient levels comparable to PAPs of other origins but are very high in Zn, Cu, and K.

Trends of water composition and discharge in the Ramganga River, Ganga Basin over the last 40 years signal enhanced nitrate flux

Studying long-term trends in river water chemistry is critical to assessing the impacts of human activities and climate change on water resources. This is of particular importance in the Indian subcontinent such as the Ganga River Basin – home to nearly 500 million people. As previous studies are mostly focused on seasonal to annual scale variabilities, the long-term riverine changes in the hydrochemistry of the rivers draining the Ganga Basin remain poorly constrained. Here we present the river chemistry and discharge data of Ramganga Basin, a major sub-catchment of Ganga River, for three hydrological stations between 1981 and 2020. Our results indicate that the total concentration of dissolved solids (TDS) within the Ramganga basin varies from 123 to 1170 mg/L and does not show a systematic spatiotemporal trend. However, we found that the fluxes of certain dissolved inorganic constituents from Ramganga Basin have significantly increased in the last 40 years with NO3– having the highest trend followed by Ca2+, Cl−, K+, SiO2, F−, and PO43−. The concentration-discharge (C–Q) analysis suggests a dominant dilution behaviour for most of the major solutes in the basin at longer timescales. We find that the cations and anions riverine loads are primarily dominated by Ca2+ and HCO3– ions, respectively, controlled by rock weathering processes, whereas the fluxes of NO3–, PO43−, and SO42− are controlled by anthropogenic processes. In summary, the long-term dataset for the Ramganga River revealed significant variability in river water chemistry, solute fluxes, and C–Q relationships over the last 40 years controlled by natural and anthropogenic processes.

Migration of copper(II) ions in humic systems—effect of incorporated calcium(II), magnesium(II), and iron(III) ions

The mobility of heavy metals in natural soil systems can be affected by the properties and compositions of those systems: the content and quality of organic matter as well as the character of inorganic constituents. In this work, the diffusion of copper(II) ions in humic hydrogels with incorporated calcium(II), magnesium(II), and iron(III) ions was investigated. The methods of instantaneous planar source and of constant source were used. Experimental data yielded the time development of the concentration in hydrogels and the values of effective diffusion coefficients. The coefficients include both the influence of the hydrogel structure and the interaction of diffusing particles with the hydrogel. Our results showed that the presence of natural metal ions such as calcium, magnesium, or iron can strongly affect the diffusivity of copper in humic systems. They indicate that the mobility of copper ions depends on their concentration. The mobility can be supported by higher contents of copper in the system. While the incorporation of Ca and Mg resulted in the decrease in the diffusivity of copper ions, the incorporation of Fe(III) into humic hydrogel resulted in an increase in the diffusivity of Cu(II) in the hydrogel in comparison with pure humic hydrogel.

Optimization of Biologically Inspired Electrospun Scaffold for Effective Use in Bone Regenerative Applications.

Human bone is composed of organic and inorganic composite materials, contributing to its unique strength and flexibility. Hydroxyapatite (HAP) has been extensively studied for bone regeneration, due to its excellent bioactivity and osteoconductivity, which makes it a highly valuable biomaterial for tissue engineering applications. For better therapeutic effects, composite nanofibers containing polyvinyl alcohol (PVA) and polyvinyl Pyrrolidone (PVP) were developed using an electrospinning technique in this study. Herein, hydroxyapatite (a major inorganic constituent of native bone) concentrations varying from 5 to 25% were reinforced in the composite, which could alter the properties of nanofibers. The as-prepared composite nanofibers were characterized by SEM, TEM, XRD, and FT-IR spectroscopy, and a bioactivity assessment was performed in simulated body fluid (SBF). The ICP-OES analysis was used to determine the concentration of Ca2+ and PO42- ions before and after SBF immersion. To optimize the material selection, the nanofibrous scaffolds were subjected to cell proliferation and differentiation in MG-63 osteoblast cell lines, but no significant toxicity was observed. In conclusion, HAP-PVA-PVP scaffolds exhibit unique physical and chemical properties and ideal biocompatibility, with great promise to serve as effective candidates for bone tissue applications.

The Decline of Paget’s Disease of Bone and Domestic Coal Use—A Hypothesis

The cause of Paget’s disease of bone (PDB) is unknown. It emerged as a distinct entity in Britain in the late nineteenth century when it was prevalent, and florid presentation not uncommon. Epidemiological surveys in the 1970s showed that Britain had a substantially higher prevalence of PDB than any other country. Studies in the late twentieth and early twenty-first centuries have documented an unexplained change in presentation, with a greatly reduced prevalence and less severe disease than formerly. The emergence of PDB in Britain coincided with rapid industrialization which, in turn, was driven by the use of coal for energy. In the home, bituminous coal was customarily burnt on an open hearth for heating. Using data on coal production, population size, and estimates of domestic use, the estimated exposure to domestic coal burning rose threefold in Britain during the nineteenth century and began to fall after 1900. This pattern fits well with the decline in PDB documented from death certification and prevalence surveys. Colonists moving from Britain to North America, Australia and New Zealand established coal mines and also used coal for domestic heating. PDB was found in these settler populations, but was largely absent from people indigenous to these lands. In all parts of the world PDB prevalence has fallen as the burning of coal in open hearths for domestic heating has reduced. The nature of the putative factor in coal that could initiate PDB is unknown, but possible candidates include both organic and inorganic constituents of bituminous coal.

Delineating the mechanisms controlling groundwater salinization using chemo-isotopic data and meta-heuristic clustering algorithms (case study: Saguenay-Lac-Saint-Jean region in the Canadian Shield, Quebec, Canada).

This study employed meta-heuristic clustering algorithms to determine the source and mechanism of groundwater salinization in Quebec's Saguenay-Lac-Saint-Jean (SLSJ) region, utilizing hydrogeochemical (38 inorganic constituents, including minor, major, and trace elements) and isotopic data (δ18O and δ2H). A total of 382 groundwater and precipitation samples were examined. Among the meta-heuristic algorithms, Artificial Bee Colony K-Means (ABCKM), Differential Evolution K-Means (DEKM), Harmony Search K-Means (HSKM), Particle Swarm Optimization K-Means (PSOKM), and Genetic K-Means (GKM) were used and investigated, and finally, PSOKM displayed superior performance and was chosen for further investigation. Analysis of diverse plots and hydrogeochemical modeling unveiled the impact of the Laflamme Sea invasion on groundwater chemistry. PSOKM1, PSOKM4, and PSOKM5 exhibited notable carbonate and silicate dissolution, with PSOKM4 demonstrating predominant carbonate dissolution. Cation exchange was identified through binary plots and Chloro Alkaline Index (CAI), with reverse cation exchange predominantly observed in most PSOKM4 samples, while positive values suggested direct cation exchange in other clusters. Spatial dynamics analysis using HFE-D indicated that salinization occurs as groundwater flows through crystalline bedrock aquifers, resulting in a transition from HCO3- dominance in PSOKM4 to Cl- dominance in the remaining clusters. Interaction between groundwater and rock along this path facilitated a transformation towards a Na-Cl end-member. The closely aligned stable isotopes with the Global Meteoric Water Line (GMWL) indicated a blend of meteoric water and seawater as the groundwater source.

Comparative functional characterization and in vitro immunological cross-reactivity studies on Daboia russelii and Craspedocephalus malabaricus venom.

Snake venom is a complex mixture of organic and inorganic constituents, including proteins and peptides. Several studies showed that antivenom efficacy differs due to intra- and inter-species venom variation. In the current study, comparative functional characterization of major enzymatic proteins present in Craspedocephalus malabaricus and Daboia russelii venom was investigated through various in vitro and immunological cross-reactivity assays. The enzymatic assays revealed that hyaluronidase and phospholipase A2 activities were markedly higher in D. russelii. By contrast, fibrinogenolytic, fibrin clotting and L-amino acid oxidase activities were higher in C. malabaricus venom. ELISA results suggested that all the antivenoms had lower binding potential towards C. malabaricus venom. For D. russelii venom, the endpoint titration value was observed at 1:72 900 for all the antivenoms. In the case of C. malabaricus venom, the endpoint titration value was 1:2700, except for Biological E (1:8100). All these results, along with the avidity assays, indicate the strength of venom-antivenom interactions. Similarly, the western blot results suggest that all the antivenoms showed varied efficacies in binding and detecting the venom antigenic epitopes in both species. The results highlight the need for species-specific antivenom to better manage snakebite victims.