Preparation, characterization, and adsorption kinetics of graphene oxide/chitosan/carboxymethyl cellulose composites for the removal of environmentally relevant toxic metals.

This study attempted to develop a low-cost and eco-friendly bio-based composite adsorbent that is highly efficient in capturing potential toxic metals. The bio-composite adsorbent was prepared using graphene oxide (GO), carboxymethyl cellulose (CMC) and chitosan (CS); and characterized using FTIR, SEM-EDX and WAXD techniques. Metal-ion concentration in an aqueous solution was measured by ICP-OES. This article reveals that the adsorption of heavy metal ions varied according to the adsorbent quantity, initial metal concentration, pH, and interaction time. The metal ions' adsorption capacity (mg/g) was observed to increase when the interaction time and metal concentration increased. Conversely, metal ions adsorption was decreased with an increase in adsorbent dosages. The effect of pH on metal ions' adsorption was ion-specific. The substantial adsorption by GO/CMC/CS composite for Co2+, CrO42-, Mn2+ and Cd2+, had the respective values of 43.55, 77.70, 57.78, and 91.38 mg/g under acidic conditions. The metal ions experimental data were best fitted with pseudo-second-order (PSO) kinetics, and Freundlich isotherm model (except Co2+). The separation factors (RL) value in the present investigation were found between 0 and 1, meaning that the metal ions adsorption onto GO/CS/CMC composite is favorable. The RL and sorption intensity (1/n) values fitted well to the adsorption isotherm.

Continuation of education after marriage and its associated factors among young adult women: findings from the Bangladesh Demographic and Health Survey 2017-2018.

OBJECTIVE: To identify the individual and community-level variables associated with the continuation of education among currently married young adult women in Bangladesh. DESIGN: Cross-sectional data extracted from the Bangladesh Demographic and Health Survey (BDHS), 2017-2018. The BDHS is a stratified cluster sample of households conducted in two and three stages in both rural and urban settings. A multilevel multinomial logistic regression analysis was employed to identify the associated factors. SETTING: Bangladesh. PARTICIPANTS: Currently married young adult women aged 15-29 years (n=4595). PRIMARY OUTCOME: Continuation of education after marriage was measured in the BDHS by asking respondents, 'Did you continue your studies after marriage?' with the response options: no; yes, less than a year; yes, for 1-2 years; yes, for 3-4 years; and yes, for 5+ years. RESULTS: Among young adult women, 28.2% continued education after marriage for different durations of years (<1 year to 5+ years). The odds of continuing education after marriage for <1 year (adjusted OR (aOR): 0.68; 95% CI 0.50 to 0.90), 1-2 years (aOR: 0.67; 95% CI 0.47 to 0.96) and ≥5 years (aOR: 0.38; 95% CI 0.17 to 0.85) were lower among women who justified wife beating compared with women who did justify it. Compared with the high-literate community, women from the low-literate community were less likely to continue education after marriage for <1 year (aOR: 0.53; 95% CI 0.42 to 0.66), 1-2 years (aOR: 0.47; 95% CI 0.36 to 0.61), 3-4 years (aOR: 0.32; 95% CI 0.22 to 0.46), and for ≥5 years (aOR: 0.29; 95% CI 0.17 to 0.48). Several other individual-level and community-level variables, such as age at marriage, first birth interval, partner educational status, household wealth index, community economic status and region, were found to be associated with the continuation of education after marriage for different durations. CONCLUSIONS: The proportion of women continuing their education after marriage in this sample is low. This study provides insight into the individual-level and community-level barriers women encounter in continuing their education after marriage. The identification of these barriers helps policy-makers develop effective intervention programmes to promote women's educational attainment.

A Comprehensive Review of the Current Progress of Chromium Removal Methods from Aqueous Solution.

Chromium (Cr) exists in aqueous solution as trivalent (Cr3+) and hexavalent (Cr6+) forms. Cr3+ is an essential trace element while Cr6+ is a dangerous and carcinogenic element, which is of great concern globally due to its extensive applications in various industrial processes such as textiles, manufacturing of inks, dyes, paints, and pigments, electroplating, stainless steel, leather, tanning, and wood preservation, among others. Cr3+ in wastewater can be transformed into Cr6+ when it enters the environment. Therefore, research on Cr remediation from water has attracted much attention recently. A number of methods such as adsorption, electrochemical treatment, physico-chemical methods, biological removal, and membrane filtration have been devised for efficient Cr removal from water. This review comprehensively demonstrated the Cr removal technologies in the literature to date. The advantages and disadvantages of Cr removal methods were also described. Future research directions are suggested and provide the application of adsorbents for Cr removal from waters.

Determination of bioavailable arsenic threshold and validation of modeled permissible total arsenic in paddy soil using machine learning.

Minimizing arsenic intake from food consumption is a key aspect of the public health response in arsenic (As)-contaminated regions. In many of these regions, rice is the predominant staple food. Here, we present a validated maximum allowable concentration of total As in paddy soil and provide the first derivation of a maximum allowable soil concentration for bioavailable As. We have previously used meta-analysis to predict the maximum allowable total As in soil based on decision tree (DT) and logistic regression (LR) models. The models were defined using the maximum tolerable concentration (MTC) of As in rice grains as per the codex recommendation. In the present study, we validated these models using three test data sets derived from purposely collected field data. The DT model performed better than the LR in terms of accuracy and Matthews correlation coefficient (MCC). Therefore, the DT estimated maximum allowable total As in paddy soil of 14 mg kg-1 could confidently be used as an appropriate guideline value. We further used the purposely collected field data to predict the concentration of bioavailable As in the paddy soil with the help of random forest (RF), gradient boosting machine (GBM), and LR models. The category of grain As (MTC) was considered as the dependent variable; bioavailable As (BAs), total As (TAs), pH, organic carbon (OC), available phosphorus (AvP), and available iron (AvFe) were the predictor variables. LR performed better than RF and GBM in terms of accuracy, sensitivity, specificity, kappa, precision, log loss, F1score, and MCC. From the better-performing LR model, bioavailable As (BAs), TAs, AvFe, and OC were significant variables for grain As. From the partial dependence plots (PDP) and individual conditional expectation (ICE) of the LR model, 5.70 mg kg-1 was estimated to be the limit for BAs in soil.

Heavy Metals in Widely Consumed Vegetables Grown in Industrial Areas of Bangladesh: a Potential Human Health Hazard.

The prevalence of heavy metals in frequently consumed vegetables constitutes a considerable public health hazard. This study aims to determine the quantity of heavy metals in widely consumed watercress (WC), alligator weed (AW), red amaranth (RA), spinach (SP), cauliflower (CF), and eggplant (EP) cultivated in industrial areas (e.g., Narsingdi district) of Bangladesh to assess the potential health hazards. Atomic absorption spectroscopy (AAS) served to determine the concentrations of lead (Pb), cadmium (Cd), chromium (Cr), and nickel (Ni) in vegetable samples (n = 72). The contents of Pb, Cd, Cr, and Ni were found in most of the analyzed vegetables, whereas 79.17%, 44.44%, and 1.39% samples exceeded the FAO/WHO maximum allowable concentration (MAC) for Pb, Cd, and Ni, respectively. The estimated daily intake (EDI) of single heavy metal was below the corresponding maximum tolerable daily intake (MTDI). The incremental lifetime cancer risk (ILCR) values of Cd in all samples exceeded the threshold limit (ILCR > 10-4) for both adults and children, indicating lifetime cancer risk due to the consumption of contaminated vegetables. The target hazard quotient (THQ) of each heavy metal was THQ < 1.0 (except Ni in few samples), indicating that consumers have no non-cancer risk when exposed to a single heavy metal. However, hazard index (HI) values of heavy metals were greater than unity in contaminated WC and AW for adults and children. Meanwhile, WC, AW, and SP samples for children emerged as potential health risks of inhabitants in the studied areas. The outcomes of the present investigation might assist the regulatory bodies concerned in setting new strategies through monitoring the quality of marketed vegetables to minimize the risks to humans.

Varietal differences influence arsenic and lead contamination of rice grown in mining impacted agricultural fields of Zamfara State, Nigeria.

In Zamfara state, Nigeria, rice is cultivated in fields contaminated with Pb (lead) from artisanal and illicit mining activities. Rice grown in such contaminated agricultural areas risks not only Pb contamination but also contamination from other toxic elements, like arsenic (As); co-contamination of Pb and As in rice cultivated in mining impacted areas has been previously reported and rice is a hyperaccumulator of As. A field study was conducted with ten different commonly-cultivated Nigerian rice varieties in the mining-impacted farmlands of Dareta village, Zamfara State. The aim was to determine the optimal rice variety for cultivation on these contaminated farmlands; an optimal variety would have the lowest contaminant concentrations and highest essential elements concentrations in the rice grains. A total of 300 paired soil and rice plants were collected. The mean As and Pb concentrations in paddy soils were 0.91 ± 0.82 mg kg-1 and 288.5 ± 464.2 mg kg-1, respectively. Mean As (30.4 ± 15.1 µg kg-1) content in rice grains was an order of magnitude lower than the Codex recommendation of 200 µg kg-1 (for milled rice) while the Pb content in all the rice varieties (overall mean of 743 ± 327 µg kg-1) was approximately four times higher than the Codex recommendation of 200 µg kg-1. Contrary to previous studies, a negative correlation was observed between As and Pb in rice grains across all the varieties. Rice variety Bisalayi was the variety with the lowest Pb transfer factor (TF = 0.08), but the average Pb concentration in rice grain was still above the Codex recommendation. Bisalayi also had the highest TF for iron. Variety ART_15, which had the lowest As uptake (TF = 0.10), had the highest TF for essential elements (magnesium, potassium, manganese, zinc, and copper). In areas of Pb contamination, Bisalayi rice may therefore be a suitable variety to choose for cultivation.

Novel electrochemical PMI marker biosensor based on quantum dot dissolution using a double-label strategy.

A novel and facile post-mortem interval (PMI) biosensor was fabricated using a double-label strategy to detect the glyceraldehyde 3-phosphate dehydrogenase (GAPDH) biomarker. A monoclonal anti-GAPDH antibody was immobilized on a surface label containing cadmium selenide quantum dots (CdSe QDs) on a cysteamine graphene oxide (Cys-GO) self-assembled monolayer. Glucose oxidase (GOx) was used as a signal label to conjugate with GAPDH. GAPDH recognition was achieved through the dissolution of the surface-attached CdSe QDs by hydrogen peroxide generated through GAPDH-conjugated GOx-catalyzed ß-glucose oxidation. To enhance sensitivity, a competitive interaction was introduced between free and conjugated GAPDH to the active site of the anti-GAPDH antibody. The electrochemical response due to CdSe dissolution decreased proportionally with the concentration of free GAPDH. Differential pulsed voltammetry was conducted to determine the analytical characteristics of the immunosensor, including the limit of detection, linear dynamic range, target selectivity, system stability, and applicability toward the analysis of real samples.

Adsorption-Desorption Behavior of Arsenate Using Single and Binary Iron-Modified Biochars: Thermodynamics and Redox Transformation.

Arsenic (As) is a dangerous contaminant in drinking water which displays cogent health risks to humans. Effective clean-up approaches must be developed. However, the knowledge of adsorption-desorption behavior of As on modified biochars is limited. In this study, the adsorption-desorption behavior of arsenate (AsV) by single iron (Fe) and binary zirconium-iron (Zr-Fe)-modified biosolid biochars (BSBC) was investigated. For this purpose, BSBC was modified using Fe-chips (FeBSBC), Fe-salt (FeCl3BSBC), and Zr-Fe-salt (Zr-FeCl3BSBC) to determine the adsorption-desorption behavior of AsV using a range of techniques. X-ray photoelectron spectroscopy results revealed the partial reduction of pentavalent AsV to the more toxic trivalent AsIII form by FeCl3BSBC and Zr-FeCl3BSBC, which was not observed with FeBSBC. The Langmuir maximum AsV adsorption capacities were achieved as 27.4, 29.77, and 67.28 mg/g when treated with FeBSBC (at pH 5), FeCl3BSBC (at pH 5), and Zr-FeCl3BSBC (at pH 6), respectively, using 2 g/L biochar density and 22 ± 0.5 °C. Co-existing anions reduced the AsV removal efficiency in the order PO4 3- > CO3 2- > SO4 2- > Cl- > NO3 -, although no significant inhibitory effects were observed with cations like Na+, K+, Mg2+, Ca2+, and Al3+. The positive correlation of AsV adsorption capacity with temperature demonstrated that the endothermic process and the negative value of Gibbs free energy increased (-14.95 to -12.47 kJ/mol) with increasing temperature (277 to 313 K), indicating spontaneous reactions. Desorption and regeneration showed that recycled Fe-chips, Fe-salt, and Zr-Fe-salt-coated biochars can be utilized for the effective removal of AsV up to six-repeated cycles.

Rare earth elements (REE) for the removal and recovery of phosphorus: A review.

There is little doubt that 'rock phosphate' reserves are decreasing, with phosphorus (P) peak to be reached in the coming decades. Hence, removal and recovery of phosphorus (P) from alternative nutrient-rich waste streams is critical and of great importance owing to its essential role in agricultural productivity. Adsorption technique is efficient, cost-effective, and sustainable for P recovery from waste streams which otherwise can cause eutrophication in receiving waters. As selective P sorption using rare earth elements (REE) are gaining considerable attention, this review extensively focuses on P recovery by utilising a range of REE-incorporated adsorbents. The review briefly provides existing knowledge of P in various waste streams, and examines the chemistry and behaviour of REE in soil and water in detail. The impact of interfering ions on P removal using REE, adsorbent regeneration for reuse, and life cycle assessment of REE are further explored. While it is clear that REE-sorbents have excellent potential to recover P from wastewaters and to be used as fertilisers, there are gaps to be addressed. Future studies should target recovery and reuse of REE as P fertilisers using real wastewaters. More field trials of synthesized REE-sorbents are highly recommended before practical application.

Lead and other elements-based pollution in soil, crops and water near a lead-acid battery recycling factory in Bangladesh.

Lead (Pb) pollution in the environment predominantly occurs through anthropogenic activities, which pose significant threats to human health and that of biota. In this study, Pb and other elements were investigated in different soils (n = 52), crops (n = 24) and water (n = 13) around a lead-acid battery (LAB) recycling workshop in southwestern Bangladesh. Most of the elements' concentrations (except Se and Ag) in soil were lower than the background concentrations. However, excessive concentrations of Pb were found in both surface (966 ± 2414 mg kg-1 at 0-15 cm) and subsurface (230 ± 490 mg kg-1 at 15-30 cm) soil. Although no definitive pattern or direction in elemental concentration in soil was observed, relatively higher concentrations of most elements were detected at the southeast part of the factory. The LAB factory, brick kiln, agricultural and geogenic activities might be the sources of these elements in soil. Extremely high amounts of Cr, As, Cd, and Pb were found in the food crops around the area. In particular, the Pb concentrations were 114 ± 155 and 665 ± 588 mg kg -1 dry weight in rice grain and straw, respectively, which reflected the emissions of Pb from the LAB recycling workshop. Moreover, 40% and 100% of the groundwater samples exceeded, respectively, the WHO provisional guideline values for As (0.01 mg L-1) and Pb (0.05 mg L-1). Consequently, a high level of Pb contamination in the soil was observed while assessing different soil pollution indices. Human health risk assessment indicated severe carcinogenic (from Pb, As, and Cr intake) and non-carcinogenic (from Pb, As, Co, Cr, Ni and Sb intake) health risks are associated with rice and groundwater consumption. It is concluded that all LAB recycling workshops should be better managed to prevent Pb pollution from seeping into the environment.

The nexus between environmental regulations, economic growth, and environmental sustainability: linking environmental patents to ecological footprint reduction in South Asia.

Environmental sustainability has become a major concern for policymakers across the globe. In this regard, understanding the factors responsible for environmental degradation is particularly important for developing nations. Against this backdrop, this study aims to evaluate the impacts of environmental regulations and other vital macroeconomic aggregates on the ecological footprints in the context of four fossil fuel-dependent South Asian countries: Bangladesh, India, Pakistan, and Sri Lanka. The major findings from the econometric analysis, accounting for cross-sectional dependency, slope heterogeneity, and structural break issues in the data, reveal that environmental regulations portray significant roles in directly and indirectly reducing the ecological footprints across South Asia. Besides, the elasticity estimates verify the authenticity of the environmental Kuznets curve and the pollution haven hypotheses. On the other hand, non-renewable and renewable energy consumptions are found to increase and decrease the ecological footprints, respectively. Moreover, renewable energy use and environmental regulations are found to jointly reduce the ecological footprints further. More importantly, environmental regulations are predicted to reduce the adverse environmental impacts of economic growth, non-renewable energy use, and foreign direct investment inflows while increasing the favorable environmental impacts associated with renewable energy use. Furthermore, the country-specific impacts of environmental regulations on the ecological footprints are found to be more or less homogeneous to the corresponding panel estimates. The environmental Kuznets curve and pollution haven hypotheses are evidenced to hold for the majority of the four South Asia nations. In line with these findings, several relevant policy-level suggestions are put forward.

Antimonate sequestration from aqueous solution using zirconium, iron and zirconium-iron modified biochars.

Antimony (Sb) is increasingly being recognized as an important contaminant due to its various industrial applications and mining operations. Environmental remediation approaches for Sb are still lacking, as is the understanding of Sb environmental chemistry. In this study, biosolid biochar (BSBC) was produced and utilized to remove antimonate (Sb(V)) from aqueous solution. Zirconium (Zr), Zirconium-iron (Zr-Fe) and Fe-O coated BSBC were synthesized for enhancing Sb(V) sorption capacities of BSBC. The combined results of specific surface area, FTIR, SEM-EDS, TEM-EDS, and XPS confirmed that Zr and/or Zr-Fe were successfully coated onto BSBC. The effects of reaction time, pH, initial Sb(V) concentration, adsorbate doses, ionic strength, temperature, and the influence of major competitive co-existing anions and cations on the adsorption of Sb(V) were investigated. The maximum sorption capacity of Zr-O, Zr-Fe, Zr-FeCl3, Fe-O, and FeCl3 coated BSBC were 66.67, 98.04, 85.47, 39.68, and 31.54 mg/g respectively under acidic conditions. The XPS results revealed redox transformation of Sb(V) species to Sb(III) occurred under oxic conditions, demonstrating the biochar's ability to behave as an electron shuttle during sorption. The sorption study suggests that Zr-O and Zr-O-Fe coated BSBC could perform as favourable adsorbents for mitigating Sb(V) contaminated waters.

Manganese in potable water of nine districts, Bangladesh: human health risk.

Safe drinking water is directly linked to good human health. An excessive amount of manganese (Mn) in drinking water supplies causes people show symptoms of neurotoxicity. In this study, the level of Mn in potable water sourced from tube wells located in 9 (nine) districts of Bangladesh was monitored. In total, 170 (one hundred and seventy) water samples were collected and Mn was quantified by atomic absorption spectroscopy (AAS). The levels of Mn found in the tube well water samples of Sirajganj, Meherpur, Chuadanga, Jhenaidah, Magura, Faridpur, Jashore, Satkhira, and Khulna were 0.37-1.86, 0.10-4.11, 0.30-0.76, 0.26-0.94, 0.01-0.18, 0.21-1.78, 0.08-1.23, 0.05-0.27, and 0.01-2.11 mg/L, respectively. Results revealed that Mn level was beyond the highest contaminated levels of 0.1 mg/L and 0.4 mg/L, which are recommended by Bangladesh Drinking Standard (BDS) and World Health Organization (WHO), respectively. The maximum Mn contaminated level reached up to 4.11 mg/L (mean, 0.53 mg/L). The Mn level in tube well water exceeded 51.1% and 75.9% set by the recommended value of WHO and BDS, respectively. Furthermore, the calculated hazard quotient (HQ) value for Mn was observed to be greater than unity, indicating both children and adults risked potential non-carcinogenic health issues. The water supply authorities should take steps to provide Mn-free drinking water for communities.

Arsenic exposure from food exceeds that from drinking water in endemic area of Bihar, India.

Extensive evidence of elevated arsenic (As) in the food-chain, mainly rice, wheat and vegetables exists. Nevertheless, the importance of exposure from food towards total As exposure and associated health risks in areas with natural occurring As in drinking water is still often neglected, and accordingly mitigations are largely focused on drinking water only. In this study, the contribution of food over drinking water to overall As exposure was estimated for As exposed populations in Bihar, India. Increased lifetime cancer risk was predicted using probabilistic methods with input parameters based on detailed dietary assessment and estimation of As in drinking water, cooked rice, wheat flour and potato collected from 91 households covering 19 villages. Median total exposure was 0.83 µg/kgBW/day (5th and 95th percentiles were 0.21 and 11.1 µg/kgBW/day) and contribution of food (median = 49%) to overall exposure was almost equal to that from drinking water (median = 51%). More importantly and contrary to previous studies, food was found to contribute more than drinking water to As exposure, even when drinking water As was above the WHO provisional guide value of 10 µg/L. Median and 95th percentile excess lifetime cancer risks from food intake were 1.89 × 10-4 and 7.32 × 10-4 respectively when drinking water As was below 10 µg/L and 4.00 × 10-4 and 1.83 × 10-3 respectively when drinking water As was above 10 µg/L. Our results emphasise the importance of food related exposure in As-endemic areas, and, perhaps surprisingly, particularly in areas with high As concentrations in drinking water - this being partly ascribed to increases in food As due to cooking in high As water. These findings are timely to stress the importance of removing As from the food chain and not just drinking water in endemic areas.

A Rare Case of Severe Neutropenia Due to Chikungunya Fever Which Improved With Filgrastim.

Chikungunya fever is a re-emerging viral illness affecting different parts of the world. Most patients recover without any serious complications. Here, we present a rare case of chikungunya fever with severe neutropenia and moderate thrombocytopenia. A 31-year-old male presented with a fever, body aches, and rash. Serial full blood counts revealed a very low neutrophil count (0.273 × 109/L) with a low platelet count (56 × 109/L). Dengue fever was excluded by doing both antigen and antibody tests. The IgM antibody against the chikungunya virus was positive. After giving one dose of granulocyte colony-stimulating factor (G-CSF) filgrastim, the neutropenia resolved. A few days later, the thrombocytopenia resolved as well. Other than episodic attacks of arthritis, he recovered completely. The absence of severe neutropenia and thrombocytopenia is considered a major demarcating feature between chikungunya fever and dengue fever. Cases like this one put physicians in a difficult position regarding accurate diagnosis and appropriate management plans. The use of filgrastim may be considered as rescue therapy in a situation like this.

Removal of arsenate from contaminated waters by novel zirconium and zirconium-iron modified biochar.

A novel biochar metal oxide composite was synthesized for effective removal of arsenate (As(V)) from aqueous solution. The materials synthesized for As(V) removal was based on a biosolid-derived biochar (BSBC) impregnated with zirconium (Zr) and zirconium-iron (Zr-Fe). The synthesized materials were comprehensively characterized with a range of techniques including Brunauer-Emmett-Teller (BET-N2) surface area, zeta potential, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results confirmed that loading of Zr and Zr-Fe onto the biochar surface was successful. The influence of pH, biochar density, ionic strength, As(V) dose rate, major anions and cations on As(V) removal was also investigated. Under all pH and reaction conditions the Zr-Fe composite biochar removed the greatest As(V) from solution of the materials tested. The maximum sorption capacity reached 15.2 mg/g for pristine BSBC (pH 4.0), while modified Zr-BSBC and Zr-FeBSBC composites achieved 33.1 and 62.5 mg/g (pH 6), respectively. The thermodynamic parameters (Gibbs free energy, enthalpy, and entropy) suggested that the adsorption process is spontaneous and endothermic. The ZrBSBC and Zr-FeBSBC showed excellent reusability and stability over four cycles. Unmodified biochar resulted in partial reduction of As(V) under oxic conditions, whilst modified biochars did not influence the oxidation state of As. All results demonstrated that the Zr and Zr-Fe BSBC composites could perform as promising adsorbents for efficient arsenate removal from natural waters.

Distribution, contamination status and source of trace elements in the soil around brick kilns.

This study reports the distribution, contamination level, and possible sources of 54 metal (oid)s in the soils found around brick kilns in south-western Bangladesh. In total, 40 soil samples were collected from the vicinity of five brick kilns in four directions at 250 m intervals. This study reveals that the mean respective concentrations of caesium (Cs), beryllium (Be), lead (Pb), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), dysprosium (Dy), holmium (Ho), terbium (Tb), erbium (Er), thulium (Tm), ytterbium (Yb), thorium (Th), germanium (Ge), yttrium (Y), zirconium (Zr), niobium (Nb), silver (Ag), hafnium (Hf), tantalum (Ta), and tungsten (W), were 7.83, 3.19, 22.93, 85.93, 9.61, 36.86, 7.30, 1.23, 5.76, 1.13, 0.99, 3.14, 0.45, 2.91, 17.72, 3.04, 30.07, 185.13, 13.99, 0.30, 5.34, 1.26, and 2.61 µg g-1. Furthermore, those amounts exceeded their respective shale values. The pollution evaluation indices indicated a moderate level of contamination by Cs, Pb, Th, Ag, Hf, Ta, W, and lanthanides but excluding lanthanum (La) and lutetium (Lu). The pollution load index revealed pollution at two brickfields. Multivariate statistics reported that coal combustion in the brick kilns is the primary source of lanthanides, actinides, Y, Zr, and Hf in the soil, while other elements derived mostly from natural sources. A portion originated from coal combustion in brick kilns and agricultural activities. Changes in metal (oid)s concentrations were non-linear with the distance between the kilns and sampling points. Consequently, further studies are required and should consider meteorological factors and severity of human impact in the study area.

Geochemical fractionation and mineralogy of metal(loid)s in abandoned mine soils: Insights into arsenic behaviour and implications to remediation.

Trace element contamination from abandoned mine sites is a major threat to the environment. The distribution of trace elements in various particle size fractions of soils from abandoned mine sites plays a critical role in designing remediation approaches. This study investigated the geochemical distribution of trace element enrichment and mineralogical composition in various particle size fractions from contrasting abandoned mine sites (Webbs Consols, Halls Peak and Mole River, Australia). Results revealed that arsenic and other element concentrations increased with decreasing particle size for samples from Webbs Consols and Halls Peak. The highest arsenic (3.05%), lead (3.23%) and zinc (1110 mg/kg) were found in the finest fraction (<0.053 mm). In Mole River, the highest concentration of arsenic (10.8%), lead (209 mg/kg) and zinc (351 mg/kg) were observed in coarse fractions. Arsenic fractionation by sequential extraction showed that arsenic was strongly associated with the amorphous and crystalline iron phases. X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies revealed that tooeleite (a ferric arsenite mineral, also confirmed by Transmission electron microscopy (TEM)), arsenopyrite, scorodite and arsenolite were the dominant arsenic minerals. The study showed elevated levels of arsenic bearing minerals across particle sizes which has significant implications for remediation approaches at abandoned mine sites.

Determinants of exclusive breastfeeding practice in Bangladesh: Evidence from nationally representative survey data.

BACKGROUND: Exclusive breastfeeding (EBF) means that an infant should be breastfed only for the first six months of life to achieve optimal child development and to prevent infant morbidity and mortality. The aim of this analysis was to determine the individual-, household-, and community-level factors associated with EBF practice in Bangladesh. METHODS: A total of 1,440 women-child pairs data were analysed extracted from 2011 and 2014 Bangladesh Demographic and Health Survey. Multilevel logistic regression models were used separately for individual-, household-, and community level factors to identify the different level of factors associated with EBF practice. RESULTS: Around 61% women in Bangladesh practiced EBF with significant variation across several individual-, household-, and community-level factors. At the individual level, higher odds of EBF practice was found among mothers' received higher number of antenatal care and lower age of child. Mothers' higher education and engagement in formal jobs were found negatively associated with EBF practice. At the community level, higher odds of EBF was found among women live in Barishal, Dhaka, and Rajshahi divisions, and resided in the community with moderate level of female education, higher level of fertility, and higher use of antenatal and delivery care. CONCLUSIONS: One in every three children in Bangladesh do not breastfeed exclusively which needs special attention for the policymakers. In this case, educated women engaged in income generating activities and women did not use antenatal care should be given priority. At the community level, priority should be given for the women's resides in the community with lower level of antenatal and delivery healthcare services use.

Deciphering the Complex Mineralogy of River Sand Deposits through Clustering and Quantification of Hyperspectral X-Ray Maps.

Alluvial mineral sands rank among the most complex subjects for mineral characterization due to the diverse range of minerals present in the sediments, which may collectively contain a daunting number of elements (>20) in major or minor concentrations (>1 wt%). To comprehensively characterize the phase abundance and chemistry of these complex mineral specimens, a method was developed using hyperspectral x-ray and cathodoluminescence mapping in an electron probe microanalyser (EPMA), coupled with automated cluster analysis and quantitative analysis of clustered x-ray spectra. This method proved successful in identifying and quantifying over 40 phases from mineral sand specimens, including unexpected phases with low modal abundance (<0.1%). The standard-based quantification method measured compositions in agreement with expected stoichiometry, with elemental detection limits in the range of <10­1,000 ppm, depending on phase abundance, and proved reliable even for challenging mineral species, such as the multi-rare earth element (REE) bearing mineral xenotime [(Y,REE)PO4] for which 24 elements were analyzed, including 12 overlapped REEs. The mineral identification procedure was also capable of characterizing mineral groups that exhibit significant compositional variability due to the substitution of multiple elements, such as garnets (Mg, Ca, Fe, Mn, Cr), pyroxenes (Mg, Ca, Fe), and amphiboles (Na, Mg, Ca, Fe, Al).