Deciphering the immunoboosting potential of macro and micronutrients in COVID support therapy

Environmental Science and Pollution Research - The immune system protects human health from the effects of pathogenic organisms; however, its activity is affected when individuals become infected....     

Hydrogeochemical assessment of carcinogenic and non-carcinogenic health risks of potentially toxic elements in aquifers of the Hindukush ranges,Pakistan: insights from groundwater pollution indexing,GIS-based,and multivariate statistical approaches

Environmental Science and Pollution Research - Globally, potentially toxic elements (PTEs) and bacterial contamination pose health hazards, persistency, and genotoxicity in the groundwater aquifer....     

Unravelling the photoprotective effects of freshwater alga Nostoc commune Vaucher ex Bornet et Flahault against ultraviolet radiations

Environmental Science and Pollution Research - Several studies have suggested the direct relationship between skin complications, air pollution, and UV irradiation. UVB radiations cause various...     

Adsorption of phosphate ions from water using a novel cellulose-based adsorbent

A novel cellulose-based adsorbent, iron(III)-coordinated amino-functionalised poly(glycidylmethacrylate)-grafted cellulose [Fe(III)–AM-PGMACell] was developed for the removal of phosphate from water and wastewater. The scanning electron micrograph showed that AM-PGMACell has a rougher surface than cellulose and the adsorption of Fe(III) on AM-PGMACell made the surface even rougher. Infrared spectroscopy revealed that amino groups on the surface of AM-PGMACell complexed with Fe(III) played an important role in the removal of phosphate from solutions. X-Ray diffraction patterns showed a decrease in crystallinity after graft copolymerisation onto cellulose. The effects of contact time, initial sorbate concentration, pH, agitation speed, dose of adsorbent and temperature on the removal process were investigated. Maximum removal of 99.1% was observed for an initial concentration of 25 mg·L ^?1 at pH 6.0 and an adsorbent dose of 2.0 g·L ^?1. A two-step pseudo-first-order kinetic model and Sips isotherm model represented the measured data very well. Complete removal of 11.6 mg·L ^?1 phosphate from fertiliser industry wastewater was achieved by 1.6 g·L ^?1 Fe(III)–AM-PGMACell. The adsorbent exhibited very high reusability for several cycles. Overall, the study demonstrated that Fe(III)–AM-PGMACell can be used as an efficient adsorbent for the removal and recovery of phosphate from water and wastewater.     

Arsenic bioaccumulation in rice and edible plants and subsequent transmission through food chain in Bengal basin: a review of the perspectives for environmental health

Arsenic (As) is a metalloid that poses serious environmental threats due to its behemoth toxicity and wide abundance. The use of arsenic-contaminated groundwater for irrigation purpose in crop fields elevates arsenic concentration in surface soil and in the plants. In many arsenic-affected countries, including Bangladesh and India, rice is reported to be one of the major sources of arsenic contamination. Rice is much more efficient at accumulating arsenic into the grains than other staple cereal crops. Rice is generally grown in submerged flooded condition, where arsenic bioavailability is high in soil. As arsenic species are phytotoxic, they can also affect the overall production of rice, and can reduce the economic growth of a country. Once the foodstuffs are contaminated with arsenic, this local problem can gain further significance and may become a global problem, as many food products are exported to other countries. Large-scale use of rainwater in irrigation systems, bioremediation by arsenic-resistant organisms and hyperaccumulating plants, and the aerobic cultivation of rice are some possible ways to reduce the extent of bioaccumulation in rice. Investigation on a complete food chain is urgently needed in the arsenic-contaminated zones, which should be our priority in future researches.     

Residue dynamics of carbendazim and mancozeb in grape (Vitis Vinifera L.) berries

The residue dynamics of carbendazim and mancozeb in grape berries is reported. The fungicides were sprayed in accordance with the most critical use pattern i.e. 4 times at 15 days interval separately at recommended and double doses. The residues of each fungicide dissipated following 1st order rate kinetics. The half-lives of carbendazim and mancozeb were 7.3 and 8.1 days at recommended dose and 4.6 and 5.7 days at double dose. Ethylenethiourea (ETU), the toxic metabolite of mancozeb was detectable at harvest following four sprays of mancozeb at recommended dose. At double dose, however, the residues of ETU could be detected even after three sprays of mancozeb. The pre-harvest intervals for carbendazim and mancozeb were found to be 26 and 12 days at recommended dose and 33 and 17 days at double dose, respectively.     

Alterations in plasma electrolyte levels of a freshwater fish Cyprinus carpio exposed to acidic pH

The impact of acidification (Low pH 5.0) on plasma electrolytes (Na⁺, K⁺, Cl^?, Ca²⁺, and Mg²⁺) in a freshwater fish Cyprinus carpio was studied for a 35 day (long term) exposure period, while control groups were maintained at neutral pH (7.3). During long-term (35 days) exposure periods, plasma K⁺ and Mg²⁺ levels were increased (77.8% and 16.0%) in the low pH (5.0) treated fish. On the other hand, plasma Na⁺, Cl^?, and Ca²⁺ levels were decreased (12.4%, 18.4% and 31.3%, respectively). The loss of plasma Na⁺, Cl^?, and Ca²⁺ indicates the displacement of Ca²⁺ from tight junctions. The increased plasma K⁺ ion might have resulted from acidosis, because intracellular K⁺ is released from muscle as H⁺ enters. The elevated level of plasma Mg²⁺ might be due to inhibition of active transport of magnesium across the kidneys resulting in the accumulation of this ion in the plasma. Ionic alteration takes place upon exposure to acidic pH and can be considered as a potential tool for detecting environmental stresses caused by acidification.     

Carbon nitride,metal nitrides,phosphides, chalcogenides,perovskites and carbides nanophotocatalysts for environmental applications

Environmental Chemistry Letters - Effective technologies and materials are needed for environmental detoxification and clean energy production. The actual photocatalytic technology is largely...     

Kinetics of degradation of carbendazim by B. subtilis strains: possibility of in situ detoxification

Food safety is a global concern due to the increased use of pesticides in agriculture. In grapes, carbendazim is one of the frequently detected fungicides. However, it is amenable to biodegradation. In this study, we aimed to assess the degradation of carbendazim by four Bacillus subtilis strains, which had earlier shown potential for biocontrol of grape diseases. In liquid medium, each of the four strains, namely, DR-39, CS-126, TL-171, and TS-204, could utilize carbendazim as the sole carbon source. The half-life was minimized from 8.4 days in the uninoculated spiked control to 4.0–6.2 days by the four strains. In Thompson Seedless sprayed with carbendazim at 1.0 g L^?1, the residue on grape berries in control was 0.44 mg kg^?1 after 25 days of application, whereas in grapes treated with the four B. subtilis strains, the residues had decreased to 0.02 mg kg^?1. The degradation kinetics showed low half-lives of 3.1 to 5.2 days in treated grapes as compared to 8.8 days in control. In inoculated soils, the half-lives were 5.9 to 7.6 days in autoclaved and 6.5 to 7.2 days in nonautoclaved soils as compared to 8.2 and 8.0 days in respective controls. The growth dynamics of these strains in all the three matrices was not affected by presence of carbendazim. Bacillus strains TS-204 and TL-171 showed higher degradation rate than the other two strains in all the three matrices and show promise for in situ biodegradation of carbendazim.     

Influence of indoor transport and mixing time scales on the performance of sensor systems for characterizing contaminant releases

Optimizing real-time sensor systems to detect and identify relevant characteristics of an indoor contaminant event is a challenging task. The interpretation of incoming sensor data is confounded by uncertainties in building operation, in the forces driving contaminant transport, and in the physical parameters governing transport. In addition, simulation tools used by the sensor interpretation algorithm introduce modeling uncertainties. This paper explores how the time scales inherent in contaminant transport influence the information that can be extracted from real-time sensor data. In particular, we identify three time scales (within room mixing, room-to-room transport, and removal from the building) and study how they affect the ability of a Bayesian Monte Carlo (BMC) sensor interpretation algorithm to identify the release location and release mass from a set of experimental data, recorded in a multi-floor building. The research shows that some limitations in the BMC approach do not depend on details of the models or the algorithmic implementation, but rather on the physics of contaminant transport. These inherent constraints have implications for the design of sensor systems.