Mechanistic Evidence for Hg Removal from Wastewater by Biologically Produced Sulfur.

A significant quantity of biologically produced sulfur (BPS) is generated as a by-product of chemical and biological desulfurization processes applied to landfill gas treatment. The beneficial upcycling of BPS has seen limited use in the environmental context. The effectiveness and underlying mechanism of BPS as an adsorbent for removing Hg2+ from both solution and wastewater were elucidated based on experiments encompassing surface characterization, adsorption isotherms, kinetics, and thermodynamics. The BPS exhibited remarkable efficacy in removing Hg2+ from solution, with the Langmuir model accurately describing the adsorption process and showing a maximum adsorption capacity of 244 mg g-1. Surface analysis through X-ray photoelectron spectroscopy and scanning electron microscopy revealed that Hg2+ complexed with sulfide on BPS surfaces, forming stable HgS. The adsorbed Hg was strongly retained in BPS, with less than 0.2% of the adsorbed Hg desorbed by strong acids. Adsorption kinetics followed the double-exponential first-order model, showing an initial rapid adsorption phase wherein 75% of the initial Hg2+ was removed within 5 min, followed by a slower adsorption rate. The thermodynamic parameters suggested that adsorption of Hg2+ by BPS was a spontaneous and endothermic process. Additionally, BPS effectively removed Hg2+ from wastewater, showing preference for Hg over other co-existing metals. These findings underscore the potential of BPS as an effective adsorbent for Hg2+ removal from wastewater.

Microbial consortia-mediated arsenic bioremediation in agricultural soils: Current status, challenges, and solutions.

Arsenic poisoning in agricultural soil is caused by both natural and man-made processes, and it poses a major risk to crop production and human health. Soil quality, agricultural production, runoff, ingestion, leaching, and absorption by plants are all influenced by these processes. Microbial consortia have become a feasible bioremediation technique in response to the urgent need for appropriate remediation solutions. These diverse microbial populations collaborate to combat arsenic poisoning in soil by facilitating mechanisms including oxidation-reduction, methylation-demethylation, volatilization, immobilization, and arsenic mobilization. The current state, problems, and remedies for employing microbial consortia in arsenic bioremediation in agricultural soils are examined in this review. Among the elements affecting their success include diversity, activity, community organization, and environmental conditions. Also, we emphasize the sensitivity and accuracy limits of existing assessment techniques. While earlier reviews have addressed a variety of arsenic remediation options, this study stands out by concentrating on microbial consortia as a viable strategy for arsenic removal and presents performance evaluation and technical problems. This work gives vital insights for tackling the major issue of arsenic pollution in agricultural soils by explaining the potential methods and components involved in microbial consortium-mediated arsenic bioremediation.

A strategy for bioremediation of nuclear contaminants in the environment.

Radionuclides released from nuclear contamination harm the environment and human health. Nuclear pollution spread over large areas and the costs associated with decontamination is high. Traditional remediation methods include both chemical and physical, however, these are expensive and unsuitable for large-scale restoration. Bioremediation is the use of plants or microorganisms to remove pollutants from the environment having a lower cost and can be upscaled to eliminate contamination from soil, water and air. It is a cheap, efficient, ecologically, and friendly restoration technology. Here we review the sources of radionuclides, bioremediation methods, mechanisms of plant resistance to radionuclides and the effects on the efficiency of biological adsorption. Uptake of radionuclides by plants can be facilitated by the addition of appropriate chemical accelerators and agronomic management, such as citric acid and intercropping. Future research should accelerate the use of genetic engineering and breeding techniques to screen high-enrichment plants. In addition, field experiments should be carried out to ensure that this technology can be applied to the remediation of nuclear contaminated sites as soon as possible.

A Simplified Method for Anionic Surfactant Analysis in Water Using a New Solvent.

Anionic surfactants (AS) are becoming a major emerging contaminant of waters due to their widespread use in household and industrial products. The standard chloroform method for analysis of AS in water relies on chloroform extraction of a methylene blue active substance (MBAS), which contains ion pairs between methylene blue (MB) molecules (positively charged) and AS. Due to the poor extractability of chloroform, the procedure is complicated, time-consuming, and subject to anionic interferences. A mixture of methyl isobutyl ketone (MIBK)-1,2-dichloroethane (DCE) at a 3:1 ratio of MIBK:DCE proved to be a robust solvent for AS extraction for a wide range of samples under various chemical conditions. The objectives of this research were to set the washing protocol to eliminate the anionic interferences in the MIBK-DCE extraction and to develop a new simplified analytical method for AS analysis using the MIBK-DCE (3:1) extractant. The suitability of the proposed MIBK-DCE method was validated based on quality control and assurance criteria, such as selectivity, accuracy, precision, method detection limit (MDL), limit of quantification (LOQ), and sensitivity. Various water samples, such as freshwater, wastewater, and seawater, were used for the method development and validation. Interferences by inorganic and organic anions were evident in the reference chloroform method but were eliminated in the MIBK-DCE procedure with a two-step process that consisted of washing with a carbonate/bicarbonate solution at pH 9.2 and a mixture of silver sulfate (Ag2SO4) and potassium alum (AlK(SO4)2). The simplified MIBK-DCE method for sodium dodecyl sulfate (SDS) analysis consisted of (i) sample pre-treatment, (ii) MIBK-DCE extraction, (iii) washing and filtration, and (iv) absorbance measurement. The MIBK-DCE method was accurate, precise, selective, and sensitive for AS analysis and showed MDL of 0.0001 mg/L, LOQ of 0.0005 mg/L, relative standard deviation (RSD) of 0.1%, and recovery of 99.0%. All these criteria were superior to those of the chloroform method. Sensitivity analysis showed highly significant correlations in AS analyses between the MIBK-DCE and chloroform methods for domestic wastewater, industrial wastewater, and seawater. The MIBK-DCE method is simple, rapid, robust, reproducible, and convenient, when compared to the chloroform method. Results demonstrate that the simplified MIBK-DCE method can be employed for AS analysis in a wide range of environmental waters including seawater.

Sources, distribution, bioavailability, toxicity, and risk assessment of heavy metal(loid)s in complementary medicines.

The last few decades have seen the rise of alternative medical approaches including the use of herbal supplements, natural products, and traditional medicines, which are collectively known as 'Complementary medicines'. However, there are increasing concerns on the safety and health benefits of these medicines. One of the main hazards with the use of complementary medicines is the presence of heavy metal(loid)s such as arsenic (As), cadmium (Cd), lead (Pb), and mercury (Hg). This review deals with the characteristics of complementary medicines in terms of heavy metal(loid)s sources, distribution, bioavailability, toxicity, and human risk assessment. The heavy metal(loid)s in these medicines are derived from uptake by medicinal plants, cross-contamination during processing, and therapeutic input of metal(loid)s. This paper discusses the distribution of heavy metal(loid)s in these medicines, in terms of their nature, concentration, and speciation. The importance of determining bioavailability towards human health risk assessment was emphasized by the need to estimate daily intake of heavy metal(loid)s in complementary medicines. The review ends with selected case studies of heavy metal(loid) toxicity from complementary medicines with specific reference to As, Cd, Pb, and Hg. The future research opportunities mentioned in the conclusion of review will help researchers to explore new avenues, methodologies, and approaches to the issue of heavy metal(loid)s in complementary medicines, thereby generating new regulations and proposing fresh approach towards safe use of these medicines.

Remediation of heavy metal(loid)s contaminated soils--to mobilize or to immobilize?

Unlike organic contaminants, metal(loid)s do not undergo microbial or chemical degradation and persist for a long time after their introduction. Bioavailability of metal(loid)s plays a vital role in the remediation of contaminated soils. In this review, the remediation of heavy metal(loid) contaminated soils through manipulating their bioavailability using a range of soil amendments will be presented. Mobilizing amendments such as chelating and desorbing agents increase the bioavailability and mobility of metal(loid)s. Immobilizing amendments such of precipitating agents and sorbent materials decrease the bioavailabilty and mobility of metal(loid)s. Mobilizing agents can be used to enhance the removal of heavy metal(loid)s though plant uptake and soil washing. Immobilizing agents can be used to reduce the transfer to metal(loid)s to food chain via plant uptake and leaching to groundwater. One of the major limitations of mobilizing technique is susceptibility to leaching of the mobilized heavy metal(loid)s in the absence of active plant uptake. Similarly, in the case of the immobilization technique the long-term stability of the immobilized heavy metal(loid)s needs to be monitored.

Partitioning hydraulic resistance in Sorghum bicolor leaves reveals unique correlations with stomatal conductance during drought.

The hydraulic architecture of leaves represents the final path along which liquid water travels through the plant and comprises a significant resistance for water movement, especially for grasses. We partitioned leaf hydraulic resistance of six genotypes of Sorghum bicolor L. (Moench) into leaf specific hydraulic resistance within the large longitudinal veins (r*LV) and outside the large veins (r*OLV), and correlated these resistances with the response of stomatal conductance (gs) and photosynthesis (A) to drought. Under well-watered conditions, gs was tightly correlated with r*OLV (r2=0.95), but as soil moisture decreased, gs was more closely correlated with r*LV (r2=0.97). These results suggest that r*OLV limits maximum rates of gas exchange, but the ability to efficiently move water long distances (low r*LV) becomes more important for the maintenance of cell turgor and gas exchange as soil moisture declines. Hydraulic resistance through the leaf was negatively correlated with evapotranspiration (P<0.001) resulting in more conservative water use in genotypes with large leaf resistance. These results illustrate the functional significance of leaf resistance partitioning to declining soil moisture in a broadly-adapted cereal species.