Hydrogen Ion Research Articles

Relationships of Jugular Bulb Parameters with Cerebral Perfusion and Metabolism After Resuscitation from Cardiac Arrest: A Post-Hoc Analysis of Experimental Studies Using a Minipig Model.

Cerebral blood flow (CBF) decreases in the first few hours or days following resuscitation from cardiac arrest, increasing the risk of secondary cerebral injury. Using data from experimental studies performed in minipigs, we investigated the relationships of parameters derived from arterial and jugular bulb blood gas analyses and lactate levels (jugular bulb parameters), which have been used as indicators of cerebral perfusion and metabolism, with CBF and the cerebral lactate to creatine ratio measured with dynamic susceptibility contrast magnetic resonance imaging and proton magnetic resonance spectroscopy, respectively. We retrospectively analyzed 36 sets of the following data obtained during the initial hours following resuscitation from cardiac arrest: percent of measured CBF relative to that at the prearrest baseline (%CBF), cerebral lactate to creatine ratio, and jugular bulb parameters, including jugular bulb oxygen saturation, jugular bulb lactate, arterial-jugular bulb oxygen content difference, cerebral extraction of oxygen, jugular bulb-arterial lactate content difference, lactate oxygen index, estimated respiratory quotient, and arterial-jugular bulb hydrogen ion content difference. Linear mixed-effects models were constructed to examine the effects of each jugular bulb parameter on the %CBF and cerebral lactate to creatine ratio. The arterial-jugular bulb oxygen content difference (P = 0.047) and cerebral extraction of oxygen (P = 0.030) had a significant linear relationship with %CBF, but they explained only 12.0% (95% confidence interval [CI] 0.002-0.371) and 14.2% (95% CI 0.005-0.396) of the total %CBF variance, respectively. The arterial-jugular bulb hydrogen ion content difference had a significant linear relationship with cerebral lactate to creatine ratio (P = 0.037) but explained only 13.8% (95% CI 0.003-0.412) of the total variance in the cerebral lactate to creatine ratio. None of the other jugular bulb parameters were related to the %CBF or cerebral lactate to creatine ratio. In conclusion, none of the jugular bulb parameters appeared to provide sufficient information on cerebral perfusion and metabolism in this setting.

The Respiratory Compensation Point: Mechanisms and Relation to the Maximal Metabolic Steady State.

At a point during the latter third of an incremental exercise protocol, ventilation begins to exceed the rate of clearance of carbon dioxide (CO2) at the lungs ( CO2). The onset of this hyperventilation, which is confirmed by a fall from a period of stability in end-tidal and arterial CO2 tensions (PCO2), is referred to as the respiratory compensation point (RCP). The mechanisms that contribute to the RCP remain debated as does its surrogacy for the maximal metabolic steady state of constant-power exercise (i.e., the highest work rate associated with maintenance of physiological steady state). The objective of this current opinion is to summarize the original research contributions that support and refute the hypotheses that: (i) the RCP represents a rapid, peripheral chemoreceptor-mediated reflex response engaged when the metabolic rate at which the buffering systems can no longer constrain the rise in hydrogen ions ([H+]) associated with rising lactate concentration and metabolic CO2 production is surpassed; and (ii) the metabolic rate at which this occurs is equivalent to the maximal metabolic steady state of constant power exercise. In doing so, we will shed light on potential mechanisms contributing to the RCP, attempt to reconcile disparate findings, make a case for its adoption for exercise intensity stratification and propose strategies for the use of RCP in aerobic exercise prescription.

Charge Transfer Mechanisms of Adaptive Multicomponent Solutions at Solid-Liquid Interfaces for Real-Time Coolant State Monitoring.

Charge-transfer mechanisms in adaptive multicomponent solutions at liquid-solid interfaces with triboelectric probes are crucial for understanding chemistry dynamics. However, liquid-solid charge transfer becomes unpredictable, due to the components or interactions in solutions, restricting its potential application for precise monitoring of liquid environments. This study utilizes triboelectric probes to investigate the charge transfer of chemicals, applying this approach to real-time coolant state monitoring. Analysis of electrical signal dynamics induced by ethylene glycol and its oxidation byproduct, oxalic acid, in ethylene glycol solutions reveals that hydrogen bond and ion adsorption diminishes the efficiency of electron transfer at the liquid-solid interface. These findings promote the engineering of the triboelectric probe that enhances coolant quality with remarkable sensitivity (detection limit: 0.0001%) and a broad freezing point operational range (0 to -49 °C). This work advances the precise control of the charge dynamics and demonstrates the potential of triboelectric probes for interdisciplinary applications.

Establishing the Thermodynamic Cards of Dipine Models' Oxidative Metabolism on 21 Potential Elementary Steps.

Dipines are a type of important antihypertensive drug as L-calcium channel blockers, whose core skeleton is the 1,4-dihydropyridine structure. Since the dihydropyridine ring is a key structural factor for biological activity, the thermodynamics of the aromatization dihydropyridine ring is a significant feature parameter for understanding the mechanism and pathways of dipine metabolism in vivo. Herein, 4-substituted-phenyl-2,6-dimethyl-3,5-diethyl-formate-1,4-dihydropyridines are refined as the structurally closest dipine models to investigate the thermodynamic potential of dipine oxidative metabolism. In this work, the thermodynamic cards of dipine models' aromatization on 21 potential elementary steps in acetonitrile have been established. Based on the thermodynamic cards, the thermodynamic properties of dipine models and related intermediates acting as electrons, hydrides, hydrogen atoms, protons, and two hydrogen ions (atoms) donors are discussed. Moreover, the thermodynamic cards are applied to evaluate the redox properties, and judge or reveal the possible oxidative mechanism of dipine models.

Химический состав и качественные показатели говядины бычков мясных пород

Purpose. To study the effect of the genotype of bulls on the chemical composition and commodity-technological parameters of beef. Materials and Methods. The object of research is 18–month-old crossbred bulls, obtained as a result of industrial crossing of Kazakh white-headed cattle bulls with heifers of Kalmyk breed (group I), Kazakh white-headed bulls with heifers of Hereford breed (group II) and Kazakh white-headed bulls with heifers of Aberdeen-Angus breed (group III). Purebred bulls of the Kazakh white-headed breed were used as a control group. The slaughter qualities of the experimental animals were determined by control slaughter of three bulls from each group. Chemical analysis of beef samples was carried out according to the following methods and GOST standards: moisture content was determined by drying the sample to a constant mass at a temperature of 100-105°C according to GOST 9793-2016; protein content – by the amount of protein nitrogen by the Kjeldahl method according to GOST 25011-2017; fat content – according to GOST 23042-2015; ash content – according to GOST 31727-2012; amino acid composition was determined according to the method of measuring the mass fraction of amino acids by the CE method on the Kapel-105M system, the concentration of hydrogen ions (pH) was determined according to GOST R 51478-99. Results. It was found that the highest slaughter qualities were possessed by crossbred bulls of the III experimental group. The highest dry matter content was in the average sample of meat of bulls of the III experimental group – 35.13%, which is 0.63% more than in the control; the difference in fat content was 0.23% in favor of the control group. In terms of protein content, the largest amount was recorded in the meat of bulls of the III experimental group – 20.07%, which is higher than in the samples of the control, I and II experimental groups, respectively, by 0.60, 0.84 and 0.77%. The protein-quality index in the samples ranged from 6.30 to 6.48. The pH value of the meat varied slightly – from 5.60 to 5.77. Conclusion. The conducted research has allowed us to establish that the industrial crossing of the Kazakh white-headed cattle with different meat breeds contributes to an increase in productivity, quality indicators, and the beef produced. This is explained by good compatibility of crossed breeds and high breed qualities of studied breeds.

Dynamics of proton intercalation into Al3+-doped vanadium oxide in an aqueous magnesium-containing electrolyte

Al3+-doped vanadium oxide (AlxV2O5) with x = 0.072 was synthesized by hydrothermal method. The presence of Al3+ ions in the layered structure of AlxV2O5 agglomerated in the form of “nanoflowers” was confirmed. The mechanism of electrochemical intercalation processes in AlxV2O5 cathodes in Mg2+-containing aqueous electrolyte was studied. The dynamics of the near-electrode electrolyte pH during charge–discharge processes was investigated by in situ pH measurements. The cyclic evolution of the electrolyte pH during the charge–discharge process suggests the direct involvement of hydrogen ions in the intercalation processes along with Mg2+-intercalation.

The unique allosteric property of crocodilian haemoglobin elucidated by cryo-EM

The principal effect controlling the oxygen affinity of vertebrate haemoglobins (Hbs) is the allosteric switch between R and T forms with relatively high and low oxygen affinity respectively. Uniquely among jawed vertebrates, crocodilians possess Hb that shows a profound drop in oxygen affinity in the presence of bicarbonate ions. This allows them to stay underwater for extended periods by consuming almost all the oxygen present in the blood-stream, as metabolism releases carbon dioxide, whose conversion to bicarbonate and hydrogen ions is catalysed by carbonic anhydrase. Despite the apparent universal utility of bicarbonate as an allosteric regulator of Hb, this property evolved only in crocodilians. We report here the molecular structures of both human and a crocodilian Hb in the deoxy and liganded states, solved by cryo-electron microscopy. We reveal the precise interactions between two bicarbonate ions and the crocodilian protein at symmetry-related sites found only in the T state. No other known effector of vertebrate Hbs binds anywhere near these sites.

Long-term trends of pH, alkalinity, and hydrogen ion concentration in an upwelling-dominated coastal ecosystem: Ría de Vigo, NW Spain

The present study focuses on the Ría de Vigo (NW Spain), a coastal embayment influenced by the Canary Current Upwelling System, which is among the world’s significant Eastern Boundary Upwelling Ecosystems. The research assesses historical changes in the marine carbonate system by generating 25-year weekly time series at six stations . Assessing ocean acidification in the region is complex due to diverse factors influencing coastal carbon dynamics, making predictions more challenging. To capture the specific dynamics in Ría de Vigo, ensembles of Neural Networks were applied. These networks were trained with a data set obtained in several oceanographic cruises, in order to retrieve pH, hydrogen ion concentration and alkalinity, achieving a root mean square error of 0.0272 pH units, 0.588 nmol kg-1\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {kg}^{-1}$$\\end{document}, and 10.6 μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}mol kg-1\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {kg}^{-1}$$\\end{document}, respectively. Subsequently, time series of the selected variables were generated, applying data of predictors measured at the aforementioned stations . An increase in normalized alkalinity was observed for all stations, except in the surface layer at the innermost location. A decrease in pH and an increase in hydrogen ion concentration were observed for all points, with trends that exceed reported rates of ocean acidification in the open ocean.

Modification of soybean lipophilic protein based on pH-shifting and high-pressure homogenization: Focus on structure, physicochemical properties and delivery vehicle

High-pressure homogenization and pH-shifting can be used to modify soybean lipophilic protein (SLP), and to enhance its ability to deliver vitamin B12. The structural changes of SLP were analyzed by multispectral techniques and the results showed that secondary and tertiary structures of SLP were altered by modification. The modification unfolded the SLP structure, released more free hydrogen ions, and increased positive charge density on the protein surface. Also, the solubility of modified SLP increased by maximum of 34.75 %. Furthermore, molecular docking showed that complexes were formed between SLP and vitamin B12 mainly through hydrogen bonding and hydrophobic interactions, and the encapsulation rate of modified SLP was maximally increased by 2.3 %. In vitro digestion showed that modified SLP enhanced stability and bioaccessibility of vitamin B12. This study provides theoretical basis for modification of SLP and effective delivery of bioactive substances.

Revisiting the statistical equilibrium of H- in stellar atmospheres

The negative hydrogen ion is, almost without exception, treated in local thermodynamic equilibrium (LTE) in the modelling of F, G, and K stars, where it is the dominant opacity source in the visual spectral region. This assumption rests in practice on a study from the 1960s. Since that work, knowledge of relevant atomic processes and theoretical calculations of stellar atmospheres and their spectra have advanced significantly, but this question has not been reexamined. We present calculations based on a slightly modified analytical model that includes H and together with modern atomic data and a grid of 1D LTE theoretical stellar atmosphere models with stellar parameters ranging from T$_ eff = 4000$ to 7000 K, $ g = 1$ to 5 cm/s$^2$, and Fe/H $=-3$ to 0. We find direct non-LTE effects on populations in spectrum-forming regions, continua, and spectral lines of about 1--2<!PCT!> in stars with higher T$_ eff $ and/or lower $ g$. Effects in models for solar parameters are smaller by a factor of 10, about 0.1--0.2<!PCT!>, and are practically absent in models with lower T$_ eff $ and/or higher $ g$. These departures from LTE found in our calculations originate from the radiative recombination of electrons with hydrogen to form exceeding photodetachment, that is, overrecombination. Modern atomic data are not a source of significant differences compared to the previous work, although detailed data for processes on resolved with vibrational and rotational states provide a more complete and complex picture of the role of in the equilibrium of In the context of modern studies of stellar spectra at the percent level, our results suggest that this question requires further attention, including a more extensive reaction network, and indirect effects due to non-LTE electron populations.

Effect of different microplastics on the mobilization of soil inorganic phosphorus by exomycorrhizal fungi

<p>Microplastics (MPs) can affect the phosphorus (P) cycle in soil by changing soil properties and the function of microbial communities, but their impact on soil P availability remains unclear. To explore the effects of different types of MPs on the mobilization of soil inorganic P by exomycorrhizal fungi, Lactarius delicious (Ld) was used as the test strain, and polystyrene microspheres (PS), polypropylene (PP) and poly(lactic acid) (PLA) were used as test materials. The soil was used as the only P source for the media. The effect of different types of MPs on the mobilization of soil inorganic P by exomycorrhizal fungi was studied using liquid culture method. The results showed that exposure to MPs at low to medium concentrations (10 or 100 mg L-1) activated inorganic P in soil by stimulating the secretion of additional organic acids and hydrogen ions by ectomycorrhizal fungi, improving the available P in soil. The effect of mobilizing inorganic P was more significant in the treatment groups exposed to low and medium concentrations of biodegradable PLA. This may be related to the fact that PLA stimulated the ectomycorrhizal fungi to secrete more organic acids, and the release of a large amount of lactic acid after PLA was biodegraded. However, when the exposure concentration of MPs further increased, the growth of ectomycorrhizal fungal mycelium may be inhibited, the secretion of organic acids and hydrogen ions may be reduced, and the mobilization ability of soil inorganic P may be limited. In addition, it should be noted that high concentrations of non biodegradable MPs (PS and PP) had significant limiting effects on the mobilization of soil inorganic P by exomycorrhizal fungi. Therefore, our study results provide evidence that the presence of MPs may reduce the availability of soil P. Further research should focus on maintaining or improving P availability in plant-microbe systems in MP-polluted soil.</p>

Climatological distribution of ocean acidification variables along the North American ocean margins

Abstract. Climatologies, which depict mean fields of oceanographic variables on a regular geographic grid, and atlases, which provide graphical depictions of specific areas, play pivotal roles in comprehending the societal vulnerabilities linked to ocean acidification (OA). This significance is particularly pronounced in coastal regions where most economic activities, such as commercial and recreational fisheries and aquaculture industries, occur. In this paper, we unveil a comprehensive data product featuring coastal ocean acidification climatologies and atlases, encompassing the fugacity of carbon dioxide, pH on the total scale, total hydrogen ion content, free hydrogen ion content, carbonate ion content, aragonite saturation state, calcite saturation state, Revelle factor, total dissolved inorganic carbon content, and total alkalinity content. These variables are provided on 1° × 1° spatial grids at 14 standardized depth levels, ranging from the surface to a depth of 500 m, along the North American ocean margins, defined as the region between the coastline and a distance of 200 nautical miles (∼370 km) offshore. The climatologies and atlases were developed using the World Ocean Atlas (WOA) gridding methods of the NOAA National Centers for Environmental Information (NCEI) based on the recently released Coastal Ocean Data Analysis Product in North America (CODAP-NA), along with the 2021 update to the Global Ocean Data Analysis Project version 2 (GLODAPv2.2021) data product. The relevant variables were adjusted to the index year of 2010. The data product is available in NetCDF (https://doi.org/10.25921/g8pb-zy76, Jiang et al., 2022b) on the NOAA Ocean Carbon and Acidification Data System: https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0270962.html (last access: 15 July 2024). It is recommended to use the objectively analyzed mean fields (with “_an” suffix) for each variable. The atlases can be accessed at https://www.ncei.noaa.gov/access/ocean-carbon-acidification-data-system/synthesis/nacoastal.html (last access: 15 July 2024).

Low-energy atomic and molecular hydrogen ion interaction with low-work function electride 12CaO · 7Al2O3

To efficiently generate H− ions from positive atomic or molecular hydrogen beams injected onto a solid surface, it has been suggested to use a material with a low-work function as the target material. However, it is not clear under what conditions the most efficient H− production is realized for incident beam parameters or reflection angles. Therefore, we studied the interaction between low-energy atomic and molecular hydrogen beams (less than 1 keV/nucleon) with a low-work function electride 12CaO⋅7Al2O3 (C12A7). The production ratio of H− to H+ ions from the C12A7 electride was much higher than Mo targets with higher work functions, especially at smaller incident and smaller reflection angles. The H− to H+ production ratio slightly increased as the incident energies were decreased, but there was no significant difference between the electride and Mo targets. These results indicate that smaller incident angles and lower beam energies of the incident hydrogen beam are favorable for the enhancement of the production ratio of H− to H+ ions in C12A7. The higher production ratio appeared at the vertical beam energies less than on the order of 100 eV, where quantum mechanical processes may become important.

Spin-Polarization Control of Photoelectrons Using Poincaré Fields.

Efficient helicity transfer from Poincaré fields to electrons of hydrogenic ions is revealed for the first time by four-dimensional relativistic simulations. The magnetic multipole class of Poincaré fields is chosen due to its fundamental role in light-matter spin coupling, and the calculation is demonstrated for Ne^{9+} ion irradiated by single and multimode x-ray pulses. Photoelectrons of both helicities emerge synchronously from the ion ensemble, and their directionality is controllable through the radiation mode numbers. The helicity density distributions display novel structures composed of jets, spirals, and rings, among others, that are unique to the combination of atomic and field parameters. Our approach to generate spin-polarized leptons using Poincaré fields may provide a new platform for helicity characterization based on advanced numerical capabilities.

New insights into kinetics and mechanisms of acid sulphite delignification of Eucalyptus globulus wood

The kinetics of Eucalyptus globulus wood delignification in Mg-base acid sulphite pulping of dissolving pulp was studied using a pilot-scale batch digester simulating the industrial process. The behavior of lignin during impregnation, heating-up and bulk delignification at the final temperature was evaluated by the analysis of acid-insoluble lignin in wood and wood residue after pulping. The dynamics of lignin dissolution was followed by its structural analysis in solid residues and in solution by wet chemistry and 1D and 2D nuclear magnetic resonance (NMR) spectroscopy. About 30 % and 20 % of the lignin were removed in the impregnation and heating-up pulping steps, respectively. About 45 % of the lignin was removed at the final pulping temperature in bulk and 3 % in the residual delignification stages. The kinetics of bulk delignification followed a pseudo-first-order kinetics with an effective activation energy of 138.4 kJ/mol in the temperature range of 140–148 °C. Bulk delignification follows an undefined overall order in the hydrogen and bisulfite ions and depended on the partial pressure of SO2 at ca. 0.60 order within the range of combined SO2 in pulping acid of 1.14–1.66 % and total SO2 loads of 6.2–7.0 %. Minimum degree of lignin sulphonation to be dissolved in the pulping liquor was suggested to be about 0.35 sulphonic groups per one phenyl propane unit. Lignin removal during pulping showed dependence on its location in different morphological parts of the fibers and related structural characteristics, which were discussed accordingly. A role of the polysaccharide complex in the accessibility of lignin was highlighted. A noticeable cleavage of β-O-4 linkages occurred in lignin already dissolved in pulping liquor at the end of cooking.

Polymer and micellar catalysis in d-fructose oxidation by imidazolium fluorochromate: A kinetic and mechanistic study

This work investigated the oxidation of d-fructose using imidazolium fluorochromate (IFC) as an oxidant and analyzed how sodium dodecyl sulfate (SDS) and polyethylene glycol (PEG-400) affected the reaction kinetics. The process exhibited a unit-order dependence on IFC, d-fructose, and perchloric acid concentration. Perchloric acid was the primary source of hydrogen ions in the reaction mixture. The stoichiometry of the reaction indicated that 3 mol of d-fructose requires 4 mol of IFC. Acrylonitrile, a radical-generating species, did not impact the reaction rate, indicating the absence of a free radical intermediate. The reaction rate decreases as the Mn (II) ions concentration increases, suggesting the involvement of Cr (IV) species in the reaction. The dielectric value of the reaction medium (D) had an inverse effect on the rate, and the outcomes were consistent with the Amis (log k1 and 1/D) and Kirkwood plots (log k1 and (D-1/2D+1)), indicating the presence of dipole-dipole interactions in the process. SDS and PEG-400 catalyzed the reaction. The reaction showed significant catalysis before reaching the critical micelle concentration (CMC). However, the observed rate constants stabilized at higher SDS concentrations exceeding the CMC. Piszkiewicz's cooperativity model was employed to describe the surfactant catalysis, while the Benesi-Hildebrand equation was utilized to explain polymer catalysis. The activation parameters are ΔH† = 44.3 ± 1.3 kJ mol−1, and ΔS† = −133.4 ± 4.3 J K−1 mol−1. The products of the reaction have been identified by spectral analysis as d-arabinoniclactone and formic acid. The formation of an ester complex followed by its decomposition was proposed as the rate-limiting step in the proposed mechanistic reaction pathway.

Transition metal catalysts coordinated with electrochemistry for preparation of graphene

It is still crucial to produce mass high-quality graphene through simple and low-cost methods for its wide applications. Herein, a simple and fast method by combining inexpensive transition metal catalysts with electrochemistry to exfoliate natural flake graphite is reported. The electrode is prepared in a sandwich structure, where the titanium mesh will enwrap the nickel net coated with graphite powder. This method can quickly achieve the large-scale preparation of graphene within 15 min. The quality of graphene with large lateral size and few layers has been characterized by XRD, SEM, TEM, Raman, and AFM. The possible electrochemical exfoliation mechanism has been proposed. Oxygen evolution reaction occurs at the anode due to the transition metal catalysts, and hydrogen ions (H+) are generated along with oxygen, H+ and SO42− ions will form a local strong acid. The formation of strong acidic H2SO4 in-situ around electrode will oxidize the edge of the graphite, allowing the intercalation of SO42−, H2O, SO2 and O2 into the graphite sheets, which will inflate the graphite and exfoliate of graphite into graphene. This strategy is reliable, environmentally friendly, and suitable for industrial production.

Central Region of the С-250 Cyclotron

The peculiarities of modeling of the central region and hydrogen ion beam dynamics for the cyclotron C-250 designed for operation in a wide energy control range of 30-250 MeV are considered. On the basis of modeling of ion beam dynamics in the energy control range, the optimal configuration of the central region of the accelerating system of the C-250 cyclotron is determined. The developed central region fulfills the requirements to ensure sufficient vertical focusing of particles by the electric field while capturing the beam in a wide phase range. The deviation of the centers ofparticle orbits from the geometric center of the cyclotron is 2-3 mm for the whole range of regulation of the cyclotron magnetic field.

Assessment of groundwater fluoride and human health effects in a hard rock province of south India: Implications from Pollution Index Model (PIM) and GeographicalInformationSystem (GIS) techniques.

This research examines whetherthe groundwater in the Sivakasi Region of South India is suitable for consumption, and assesses the possible health hazards for various age demographics including infants, children, teenagers, and adults. A totalof 77 groundwater samples were gathered, covering a total area of 580km2 and analyzed for major and minor ions. The hydrogen ion concentration (pH) of the samples indicates neutral to marginally alkaline. The total dissolved solids (TDS) fluctuate from 255 to 2701mg/l and electrical conductivity varies from 364 to 3540µS/cm. A wide range of fluoride concentration was detected (0.1 to 3.2mg/l) with nearly 38% groundwater samples surpassing the proposed limit (1.5 mg/l) suggestedby the World Health Organization in 2017. Gibbs plot analysis suggested that most of thesamples were influenced by geogenic factors, primarily rock weathering in this region. Correlation analysis showed that most of the samples were impacted by both natural and human sources. The pollution index of groundwater (PIG) fluctuated from 0.67 to 2.60 with approximately 30% and 53% of samples falling into insignificant and low pollution categories, respectively. Furthermore, 10% and 5% of total samples were characterized as moderate and high pollution levels, and 2% asvery high pollution category. Spatial analysis using GIS revealed that 440.63km2 were within safe fluoride levels according to theWHO standards, while 139.32km2 were identified as risk zone. The principal component analysis (PCA1) showedstrong positive loadings on EC (0.994), TDS (0.905), Mg2+ (0.910), Cl- (0.903) and HCO3- (0.923) indicating rock water interaction. PCA2 accounts the high positive factor loading on HCO3- (0.864) indicating ion exchange and mineral leaching. The PCA1 and PCA2 indicated that variables such as mineral leaching and rock water interaction are themajor mechanisms contributing to the chemical signatures in groundwater, which may support for theelevated fluoride levels in certain areas. Risk assessments, including Hazard Quotient results showed that 71%, 61% 38%, and 34% of groundwater samples exceededthe permissible THI limit (THI > 1) for infants, children, teenagers, and adults, respectively. The study recommends implementing measures such as denitrification, defluorination, rainwater harvesting, and improved sanitation infrastructure to enhance the health conditions in the study region. Additionally, it suggests introducing educational programs in rural areas to create awarenessabout the health dangers due to consumptionof water with high fluoride levels.

Discovery of a damped Ly α absorber in the circumnuclear zone of the FeLoBAL quasar SDSS J083942.11+380526.3

ABSTRACT SDSS J083942.11+380526.3 ($z=2.315$) is an iron low-ionization broad absorption lines quasar that exhibits visible Balmer absorption lines (H $\alpha$), implying a significant $n=2$ population. The quasar also shows an array of absorption lines, including O i, Ni ii, Fe ii, Mg ii, Al iii to C iv, and N v. The high-ionization absorption lines such as C iv and Si iv are revealed by slightly blueshifted broad absorption lines troughs. The resonance doublets such as Mg ii and Al iii are saturated but did not reached zero intensity which indicates that the broad-line region (BLR) is partially covered. Overall, however, the absorption is predominantly from low-ionization Fe ii lines, emitted from ground and excited states up to at least 3.814 eV. This implies that the absorbing gas spans the hydrogen ionization front and extends into the partially ionized zone where neutral hydrogen is certainly present. Notably, the hydrogen line spectrum of the quasar shows no signature of expected Ly $\alpha$ absorption. Instead, the line spectrum shows an unusual Ly $\alpha$ emission characterized by a fully filled emission line spectrum which is a composite of a strong narrow core superposed on a weak broad base. Taking into account the effect of partial covering to BLR, we have extracted a strong Damped Ly α systems (DLA) trough in Ly $\alpha$ emission region. To fit the spectrum, we performed photoionized model calculations and compared them to the observations. We found that photoionization modelling using cloudy can successfully reproduce the main characteristics of the quasar spectrum, and the predicted neutral hydrogen column density arising from the clouds responsible for the low-ionization absorption provides a good match to the extracted DLA trough. This indicates that both the DLA and the low-ionization absorption arise from the same medium that is roughly collocated with the dusty torus.