Enhancing the Photocatalytic Degradation of Methylene Blue with Graphene Oxide-Encapsulated g-C3N4/ZnO Ternary Composites.

Methylene blue (MB) is a toxic contaminant present in wastewater. Here, we prepared various composites of graphene oxide (GO) with graphitic carbon nitride (g-C3N4) and zinc oxide (ZnO) for the degradation of MB. In comparison to ZnO (22.9%) and g-C3N4/ZnO (76.0%), the ternary composites of GO/g-C3N4/ZnO showed 90% photocatalytic degradation of MB under a light source after 60 min. The experimental setup and parameters were varied to examine the process and effectiveness of MB degradation. Based on the results of the experiments, a proposed photocatalytic degradation process that explains the roles of GO, ZnO, and g-C3N4 in improving the photocatalytic efficacy of newly prepared GO/g-C3N4/ZnO was explored. Notably, the g-C3N4/ZnO nanocomposite's surface was uniformly covered with ZnO nanorods. The images of the samples clearly demonstrated the porous nature of GO/g-C3N4/ZnO photocatalysts, and even after being mixed with GO, the g-C3N4/ZnO composite retained the layered structure of the original material. The catalyst's porous structure plausibly enhanced the degradation of the contaminants. The high-clarity production of g-C3N4 and the effectiveness of the synthesis protocol were later validated by the absence of any trace contamination in the energy-dispersive X-ray spectroscopy (EDS) results. The composition of the ZnO elements and their spectra were revealed by the EDS results of the prepared ZnO nanorods, g-C3N4/ZnO, and GO/g-C3N4/ZnO. The outcomes indicated that the nanocomposites were highly uncontaminated and contained all necessary elements to facilitate the transformative process. The results of this experiment could be applied at a large scale, thus proving the effectiveness of photocatalysts for the removal of dyes.

Biochar/nano-zerovalent zinc-based materials for arsenic removal from contaminated water.

In this study, we explored the potential of a newly prepared nano-zero valent zinc (nZVZn), biochar (BC)/nZVZn and BC/hydroxyapatite-alginate (BC/HA-alginate) composites for the removal of inorganic As species from water. Relatively, higher percentage removal of As(III) and As(V) was obtained by nZVZn at pH 3.4 (96% and 94%, respectively) compared to BC/nZVZn (90% and 88%) and BC/HA-alginate (88% and 80%) at pH 7.2. Freundlich model provided the best fit (R2 = up to 0.98) for As(III) and As(V) sorption data of all the sorbents, notably for nZVZn. The pseudo-second order model well-described kinetics of As(III) and As(V) (R2 = 0.99) sorption on all the sorbents. The desorption experiments demonstrated that the As removal efficiency, up to the third sorption/desorption cycle, was in the order of nZVZn ∼ BC/HA-alginate (88%) > BC/nZVZn (84%). The Fourier transform infrared spectroscopy depicted that the -OH, -COOH, Zn-O and Zn-OH surface functional groups were responsible for the sorption of As(III) or As(V) on the sorbents investigated here. This study highlights that removal of As species from water by BC/nZVZn composite can be compared with nZVZn, suggesting that integrating BC with nZVZn could efficiently remove As from As-contaminated drinking water.

This is the first study to explore the potential of a newly prepared sugarcane bagasse biochar/nano-zerovalent zinc (BC/nZVZn) based composite for the removal of inorganic arsenic (As) species from water. The results indicated high percentage removal of As(III) and As(V) from water by BC/nZVZn that were comparable to nZVZn alone.

Microwave Irradiation and Glutamic Acid-Assisted Phytotreatment of Tannery and Surgical Industrial Wastewater by Sorghum.

We investigated how different doses of microwave irradiation (MR) affect seed germination in Sorghum, including the level of remediation against textile and surgical wastewater (WW) by modulating biochemical and morpho-physiological mechanisms under glutamic acid (GA) application. The experiment was conducted to determine the impact of foliar-applied GA on Sorghum under wastewater conditions. Plants were treated with or without microwave irradiation (30 s, 2.45 GHz), GA (5 and 10 mM), and wastewater (0, 25, 50, and 100). Growth and photosynthetic pigments were significantly decreased in plants only treated with various concentrations of WW. GA significantly improved the plant growth characteristics both in MR-treated and -untreated plants compared with respective controls. HMs stress increased electrolyte leakage (EL), hydrogen peroxide (H2O2), and malondialdehyde (MDA) content; however, the GA chelation significantly improved the antioxidant enzymes activities such as ascorbate oxidase (APX), superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) both in MR-treated and -untreated plants under WW stress compared with respective controls. The results suggested that the MR-treated plants accumulate higher levels of HMs under GA addition in comparison to the WW-only-treated and MR-untreated plants. The maximum increase in Cd accumulation was observed in the range of 14-629% in the roots, 15-2964% in the stems, and 26-4020% in the leaves; the accumulation of Cu was 18-2757% in the roots, 15-4506% in the stems, and 23-4605% in the leaves; and the accumulation of Pb was 13-4122% in the roots, 21-3588% in the stems, and 21-4990% in the leaves under 10 mM GA and MR-treated plants. These findings confirmed that MR-treated sorghum plants had a higher capacity for HMs uptake under GA and could be used as a potential candidate for wastewater treatment.

Enhanced Solar Photocatalytic Reduction of Cr(VI) Using a (ZnO/CuO) Nanocomposite Grafted onto a Polyester Membrane for Wastewater Treatment.

Among chemical water pollutants, Cr(VI) is a highly toxic heavy metal; solar photocatalysis is a cost-effective method to reduce Cr(VI) to innocuous Cr(III). In this research work, an efficient and economically feasible ZnO/CuO nanocomposite was grafted onto the polyester fabric ZnO/CuO/PF through the SILAR method. Characterization by SEM, EDX, XRD, and DRS confirmed the successful grafting of highly crystalline, solar active nanoflakes of ZnO/CuO nanocomposite onto the polyester fabric. The grafting of the ZnO/CuO nanocomposite was confirmed by FTIR analysis of the ZnO/CuO/PF membrane. A solar photocatalytic reduction reaction of Cr(VI) was carried out by ZnO/CuO/PF under natural sunlight (solar flux 5-6 kW h/m2). The response surface methodology was employed to determine the interactive effect of three reaction variables: initial concentration of Cr(VI), pH, and solar irradiation time. According to UV/Vis spectrophotometry, 97% of chromium was removed from wastewater in acidic conditions after four hours of sunlight irradiation. ZnO/CuO/PF demonstrated reusability for 11 batches of wastewater under natural sunlight. Evaluation of Cr(VI) reduction was also executed by complexation of Cr(VI) and Cr(III) with 1, 5-diphenylcarbazide. The total percentage removal of Cr after solar photocatalysis was carried out by AAS of the wastewater sample. The ZnO/CuO/PF enhanced the reduction of Cr(VI) metal from wastewater remarkably.

Effective Removal of Cr(VI) from Wastewater Using Biochar Derived from Walnut Shell.

Heavy metals are the major concern of the modern age. Among the heavy metals, chromium (Cr(VI)) is regarded as a highly toxic heavy metal released largely from leather tanning operations. To remove such high concentrations of Cr(VI), an advanced method is required urgently. Thus, biosorption using biochar, which is an organic material produced from various sources such as walnut shell, can be applied successfully for Cr(VI) abatement. The major objectives of this experiment were the remediation of the Cr(VI) heavy metal using walnut shell biochar and checking of the effect of pH, biochar dosage, Cr level, and shaking time. Remediation of Cr(VI) using walnut shell biochar was proved to be effective and removed the maximum concentration of Cr(VI) up to 93% at pH 5.5, 2 h agitation time, and the biochar amount of 1.1 g L-1 from an aqueous solution. Equilibrium modeling demonstrated that the chemisorption process was involved in adsorption of Cr(VI). The surface of the biochar was porous and provided numerous sites for Cr(VI) attachment, which was also confirmed by the presence of Cr(VI) onto the biochar after adsorption. Hence, the use of walnut shell biochar was highly effective as a sorbent, which could conveniently be applied to small-scale as well as large-scale levels.

Efficacy of Lemna minor and Typha latifolia for the treatment of textile industry wastewater in a constructed wetland under citric acid amendment: A lab scale study.

Lead (Pb), copper (Cu) and chromium (Cr) are one of the most harmful heavy metals (HMs), entering into the food chain through the irrigation of crops with an industrial effluent. The present study was performed to evaluate the toxic effects of textile effluents and performance of citric acid (CA) on phytoextraction potential of Lemna minor L. and Typha latifolia L. in an artificially designed wetland. Different doses of textile wastewater (0, 25, 50, 75, and 100%) and CA (10 mM) were applied alone and in combination. Plants were harvested and the data was collected regarding agronomic traits, photosynthetic pigments, antioxidant enzymes, reactive oxygen species (ROS), electrolytic leakage (EL) and HMs uptake and accumulation. The results depicted that the concentration and accumulation of Cu, Pb and Cr in different parts of T. latifolia plant was increased with and without CA addition. The maximum concentration of Pb, Cu and Cr increased in leaves by 279, 240 & 171%, in stem by 192, 172 & 154%, and in roots by 224, 183 & 168%, respectively. Similarly, the accumulation of Pb, Cu and Cr increased in leaves by 91, 71 & 36%, in stem by 57, 46 & 36% and in roots by 76, 53 & 45%, respectively in plants treated with 100% textile effluent as compared to the 25% textile effluent treated plants under CA amendment. In L. minor, the concentration of Pb, Cu & Cr increased by 542, 411 and 397% while accumulation increased by 101, 59 & 55% respectively in overall plant biomass.

Engineered biochars for recovering phosphate and ammonium from wastewater: A review.

Biochar has gained great scientific attention as a promising agent for agricultural and environmental applications. A variety of biochars with excellent properties such as high porosity, surface area and functional groups have been developed for nutrients recovery from wastewater. Compared to pristine biochar, engineered biochar with enlarged surface area and abundant functional groups has been prepared which shows a new type of carbon-based material with enhanced adsorption potential for nutrients in wastewater. To date, a few reviews have been specifically focused on several important aspects of engineered biochar, such as its application to recover phosphate and ammonium from wastewater and subsequent use as a slow-release fertilizer. In this work, novel modification/treatment methods including activation with acid/alkali, functionalization with amides, thiols and oxidizing agents, metal salt impregnation, loading with various minerals and carbon-based materials are reviewed for preparing engineered biochar with improved adsorption capacity. Various sources of biomass for producing biochars were estimated, and the intrinsic characteristics and potential of biochar products for simultaneous recovery/removal of phosphate and ammonium from wastewater were evaluated. Relevant interaction mechanisms of phosphate and ammonium adsorption on engineered biochars have been discussed in details. Finally, important future prospects as well as industrial/commercial-scale application of engineered biochars for phosphate and ammonium recovery from wastewater have been emphasized. We believe that this review will provide broad scientific opportunities for thorough understanding of applying engineered biochar as a low-cost and environmentally sustainable material for nutrients recovery from wastewater.

Effect of green and chemically synthesized titanium dioxide nanoparticles on cadmium accumulation in wheat grains and potential dietary health risk: A field investigation.

A field study was designed to explore the impacts of foliar-applied chemically and green synthesized titanium dioxide nanoparticles (TiO2 NPs) on cadmium (Cd) uptake in wheat plants. The wheat was grown in field which was contaminated with Cd and plants were subjected to foliar episodes of TiO2 NPs during plant growth period. Leaf extracts of two plant species (Trianthema portulacastrum, Chenopodium quinoa) were used for green synthesis while sol-gel method was used for chemical preparation of TiO2 NPs. Results showed that TiO2 NPs significantly enhanced the plant height, length of spikes photosynthesis, and straw and grain yield compared to control. TiO2 NPs minimized the oxidative burst in leaves and improved the enzyme activities than control. Cadmium concentrations of straw, roots and grains decreased after TiO2 NPs treatments than control. The grain Cd contents were below recommended threshold (0.2 mg Cd /kg grain DW) for cereals upon NPs exposure. The health risk index by the dietary use of grains for adults was below threshold upon NPs exposure. Overall, foliar use of TiO2 NPs prepared from plant extracts was appropriate in minimizing Cd contents in wheat grains, thereby reducing risk of Cd to human health via food chain.

Arsenic biogeochemical cycling in paddy soil-rice system: Interaction with various factors, amendments and mineral nutrients.

Arsenic (As) contamination is a well-recognized environmental and health issue, threatening over 200 million people worldwide with the prime cases in South and Southeast Asian and Latin American countries. Rice is mostly cultivated under flooded paddy soil conditions, where As speciation and accumulation by rice plants is controlled by various geo-environmental (biotic and abiotic) factors. In contrast to other food crops, As uptake in rice has been found to be substantially higher due to the prevalence of highly mobile and toxic As species, arsenite (As(III)), under paddy soil conditions. In this review, we discussed the biogeochemical cycling of As in paddy soil-rice system, described the influence of critical factors such as pH, iron oxides, organic matter, microbial species, and pathways affecting As transformation and accumulation by rice. Moreover, we elucidated As interaction with organic and inorganic amendments and mineral nutrients. The review also elaborates on As (im)mobilization processes and As uptake by rice under the influence of different mineral nutrients and amendments in paddy soil conditions, as well as their role in mitigating As transfer to rice grain. This review article provides critical information on As contamination in paddy soil-rice system, which is important to develop suitable strategies and mitigation programs for limiting As exposure via rice crop, and meet the UN's key Sustainable Development Goals (SDGs: 2 (zero hunger), 3 (good health and well-being), 12 (responsible consumption and production), and 13 (climate action)).

High sorption efficiency for As(III) and As(V) from aqueous solutions using novel almond shell biochar.

Arsenic (As) presence in surface reservoirs and groundwater is considered as an extremely alarming issue around the globe. The objectives of the present study were to evaluate the sorption potential of almond shell (ALS) and almond shell biochar (ASB) based sorbents for the removal of As(III)/As(V) from As-contaminated aqueous solutions. The maximum As(III) sorption capacity of ALS and ASB were 4.6 and 4.86 mg g-1, respectively at an initial As concentration of 5 mg L-1, pH ∼ 7.2 and sorbent dose of 0.6 g L-1. Similarly, in case of As(V) the maximum sorption capacities were reported as 3.45 and 3.6 mg g-1 by ALS and ASB respectively. Almond shell biochar removed 10-25% higher As(III)/As(V) compared to the ALS. The isotherm modeling results revealed that both for As(III) and As(V), Langmuir model presented the suitable fit to the equilibrium data compared to other model showing the monolayer sorption to be a dominant sorption mechanism. The FTIR and XPS spectroscopy revealed that mostly -OH functional groups along with some other aromatic and/or aliphatic carbon- and oxygen-rich groups (CC-C, -C-H, CO) were responsible for As sorption by both sorbents. It is concluded that ASB can remove As, notably As(III) from water more efficiently compared to natural ALS. Overall, the results of this research reveal that biochar conversion of ALS can enhance the sorption capacity for As in contaminated waters such as drinking water and wastewater.

A review of biochar-based sorbents for separation of heavy metals from water.

Biochar is the low-cost and environmental-friendly material which has shown a great potential for separation of heavy metals from water. The previous studies have established a superior role of biochar over other materials, such as activated carbon and inorganic sorbents (iron based) in efficient removal of toxic heavy metals from aqueous systems. Among the various factors influencing heavy metals sorption ability of biochar, types of feedstock/biomass and pyrolysis temperature play a significant role. The goal of this review is to increase our understanding of heavy metals sorption behavior by biochars - this is important as heavy metals sorption is driven based on biochar type, heavy metals species which involve numerous mechanisms, including the physical binding, complexation, ion exchange, surface precipitation and electrostatic interactions. In addition, this review paper describes various approaches to improve heavy metal sorption capacity of biochars by steam and acids/bases activations and impregnation of biochar-based composites with minerals, organic compounds and carbon-rich materials. The physical/chemical activation of biochars can improve the surface area, thus leading to their improved functionality, while modification/pretreatment methods help in synthesizing composites using biochar as a supporting media to develop new sorbents with efficient surface attributes for heavy metals removal from aqueous solutions.

Comparative efficiency of peanut shell and peanut shell biochar for removal of arsenic from water.

Contamination of surface water and groundwater streams with carcinogenic chemicals such as arsenic (As) has been a major environmental issue worldwide, and requires significant attention to develop new and low-cost sorbents to treat As-polluted water. In the current study, arsenite (As(III)) and arsenate (As(V)) removal efficiency of peanut shell biochar (PSB) was compared with peanut shell (PS) in aqueous solutions. Sorption experiments showed that PSB possessed relatively higher As removal efficiency than PS, with 95% As(III) (at pH 7.2) and 99% As(V) (at pH 6.2) with 0.6 g L-1 sorbent dose, 5 mg L-1 initial As concentration, and 2 h equilibrium time. Experimental data followed a pseudo-second-order model for sorption kinetics showing the dominance of chemical interactions (surface complexation) between As and surface functional groups. The Langmuir model for sorption isotherm indicated that As was sorbed via a monolayer sorption process. The X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy analyses revealed that the hydroxyl (-OH) and aromatic surface functional (C=O, C=C-C, and -C-H) groups contributed significantly in the sorption of both As species from aqueous solutions through surface complexation and/or electrostatic reactions. We demonstrate that the pyrolysis of abandoned PS yields a novel, low-cost, and efficient biochar which provides dual benefits of As-rich water treatment and a value-added sustainable strategy for solid waste disposal.

Exploring the arsenic removal potential of various biosorbents from water.

Globally, contamination of groundwater with toxic arsenic (As) is an environmental and public health issue given to its carcinogenic properties, thereby threatening millions of people relying on drinking As-contaminated well water. Here, we explored the efficiency of various biosorbents (egg shell, java plum seed, water chestnut shell, corn cob, tea waste and pomegranate peel) for arsenate (As(V)) and arsenite (As(III)) removal from As-contaminated water. Significantly, egg shell and java plum seed displayed the greatest As(III) elimination (78-87%) at 7 pH followed by water chestnut shell (75%), corn cob (67%), tea waste (74%) and pomegranate peel (65%). In contrast, 71% and 67% of As(V) was removed at pH 4.1 and 5.3 by egg shell and java plum seed, respectively. The maximum As(V) and As(III) sorption by all the biosorbents was obtained, notably for egg shell and java plum seed, after 2 h contact time. Langmuir isotherm and pseudo-second order models best fitted the sorption data for both forms of As. The -OH, -COOH, -NH2 and sulfur-bearing surface functional groups were possibly involved for As(III) and As(V) removal by biosorbents. The scanning electron microscopy combined with the energy dispersive X-ray spectroscopy (SEM-EDX) analysis showed that the heterogeneous surface of biosorbents, possessing rough and irregular areas, could have led to As sorption. Both As(V) and As(III) were successfully desorbed (up to 97%) from the biosorbents in four sorption/desorption (regeneration) cycles. This pilot-scale study highlights that egg shell and java plum seed have the greatest ability to remove both As species from As-contaminated drinking water. Importantly, these findings provide insights to develop an inexpensive, effective and sustainable filtration technology for the treatment of As in drinking water, particularly in developing countries like Pakistan.

Arsenic removal by natural and chemically modified water melon rind in aqueous solutions and groundwater.

Contamination of groundwater with toxic arsenic (As) has become an emerging health and environmental problem around the world, which has seen significant attention amongst the scientists for development of new sorbents to remediate As-contaminated water. Here, we explored the arsenate (As(V)) and arsenite (As(III)) sorption to natural water melon rind (WMR), xanthated WMR and citric acid-modified WMR in aqueous solutions, and determined potential of the most potent sorbent for As removal in groundwater. Xanthated WMR (X-WMR) showed relatively higher As(V) and As(III) removal than the citric acid modified WMR (CA-WMR) and natural WMR. The maximum As(III) (99%) and As(V) (98%) removal was obtained at pH 8.2 and 4.6, respectively, by X-WMR at 4 mg L-1 initial As(V) and As(III) concentrations and sorbent dose of 1 g L-1. Langmuir isotherm model best fitted (R2 of up to 0.96) the data both for As(III) and As(V) sorption to X-WMR. Sorption kinetics of As(V) and As(III) was well described (R2 of up to 0.99) by the pseudo second-order model on surface of the X-WMR. Thermodynamic investigations revealed that As(V) and As(III) sorption was endothermic and spontaneous. The FTIR spectroscopy depicted the presence of different surface function groups (OH, COOH, S-bearing (C=S, S=O and S-S)) which were involved in As(V) and As(III) sequestration on the sorbents examined here. Significantly, X-WMR showed (up to 49%) greater As(III) and As(V) sorption than that of natural WMR. Our results demonstrated that X-WMR efficiently removed 94%-100% (n = 16) of As from As-contaminated drinking well water which possessed detectable concentrations of some anions (e.g., SO4, CO3, HCO3). This study highlights that the X-WMR has potential to remove As, notably As(III), from solutions and drinking water, and might be utilized as a reactive medium for the treatment of As-contaminated water.

The evaluation of arsenic contamination potential, speciation and hydrogeochemical behaviour in aquifers of Punjab, Pakistan.

In this study, we tested 123 groundwater wells from five different areas of Punjab, Pakistan for arsenic (As) contamination level and species, as well as delineated hydrogeochemical behaviour of As in aquifers. Results revealed that 75% and 41% of the groundwater wells exceeded the safe As limit of World Health Organisation (WHO, 10 µg L-1) and Pakistan-EPA (50 µg L-1), respectively. Arsenite (As(III)) and arsenate (As(V)) spanned 0-80% and 20-100% of total As (1.2-206 µg L-1), respectively. The mean As content (5.2 µg L-1) of shallow wells at 9-40 m depth did not exceed the WHO safe limit, representing a safe aquifer zone for pumping of groundwater compared to deeper wells at 41-90 m (51 µg L-1) and >90 m (23 µg L-1) depths. Piper-plot elucidated that the aqueous chemistry was dominated with Na-SO4, Na-Ca-SO4, Na-Mg-SO4 type saline water. Principal component analysis grouped As concentration with well depth, pH, salinity, Fe and CO3, exhibiting that these hydrogeochemical factors could have potential role in controlling As release/sequestration into the aquifers of study area. Geochemical modeling showed positive saturation indices only for iron (Fe) oxide-phases, indicating Fe oxides as the major carriers of As. Overall, this study provides insights to tackle emerging As threat to the communities in Punjab, Pakistan, as well as help develop suitable management/mitigation strategies - based on the baseline knowledge of As levels/species and factors governing As contamination in the study area.

Drinking Water Quality Status and Contamination in Pakistan.

Due to alarming increase in population and rapid industrialization, drinking water quality is being deteriorated day by day in Pakistan. This review sums up the outcomes of various research studies conducted for drinking water quality status of different areas of Pakistan by taking into account the physicochemical properties of drinking water as well as the presence of various pathogenic microorganisms. About 20% of the whole population of Pakistan has access to safe drinking water. The remaining 80% of population is forced to use unsafe drinking water due to the scarcity of safe and healthy drinking water sources. The primary source of contamination is sewerage (fecal) which is extensively discharged into drinking water system supplies. Secondary source of pollution is the disposal of toxic chemicals from industrial effluents, pesticides, and fertilizers from agriculture sources into the water bodies. Anthropogenic activities cause waterborne diseases that constitute about 80% of all diseases and are responsible for 33% of deaths. This review highlights the drinking water quality, contamination sources, sanitation situation, and effects of unsafe drinking water on humans. There is immediate need to take protective measures and treatment technologies to overcome unhygienic condition of drinking water supplies in different areas of Pakistan.

Foliar application of aspartic acid lowers cadmium uptake and Cd-induced oxidative stress in rice under Cd stress.

Cadmium (Cd) contamination of farmland soils is a widespread problem around the globe, and rice (Oryza sativa L.) tends to accumulate more Cd and is considered as one of the major sources of Cd intake in humans, especially consuming rice-derived products. The current study investigated the effects of foliar applied aspartic acid (Asp) on growth parameters, biomass, chlorophyll concentration, gas exchange characteristics, Cd uptake, and antioxidative capacity in the shoots and roots of rice seedlings exposed to Cd stress. For this, 30-day-old rice nursery was transferred in the soil with aged Cd contamination (2.86 mg kg-1). After 2 weeks of growth, different concentrations (0, 10, 15, and 20 mg L-1) of Asp were foliar applied four times with a 7-day interval, and the crop was harvested after 10 weeks of transplanting. Foliar applied Asp increased the plant height, shoot and root dry weight, chlorophyll concentration, and gas exchange parameters, while it reduced the Cd concentrations in both shoots and roots as well as shoot to root Cd translocation factor compared to the control. Foliar application of Asp reduced the malondialdehyde content and electrolyte leakage in rice parts compared to the control in a dose-additive manner. The activities of key antioxidant enzymes increased while peroxidase activity decreased by exogenous Asp. The increase in plant weight and photosynthesis might be due to lower Cd concentrations in plants which may reduce the oxidative stress and also help the plants to minimize direct damage caused by Cd to the photosynthetic organs.

Effect of zinc-lysine on growth, yield and cadmium uptake in wheat (Triticum aestivum L.) and health risk assessment.

Cadmium (Cd) is among the most widespread toxic trace elements found in agricultural soils due to various anthropogenic activities. The role of micronutrient-amino chelates on reducing Cd toxicity in crop plants is recently introduced. The current study was conducted to highlight the role of foliar application of zinc-lysine (Zn-lys) complex on biochemical and growth parameters and Cd uptake in wheat (Triticum aestivum) grown in aged Cd-contaminated soil. Foliar concentration of Zn-lys (0, 10, 20, and 30 mg L-1) was applied at different time intervals (2nd, 3rd, 5th and 7th week of sowing) and plants were harvested at maturity. Folliar application of Zinc-lys significantly increased the photosynthesis, grain yield, enzyme activities and Zn contents in different plant tissues. Zinc-lys reduced Cd contents in grains, shoot and root as well as reduced the oxidative stress in wheat linearly in a dose-additive manner. Taken together, Zn-lys chelate efficiently improved wheat growth and fortified Zn contents while reduced Cd concentration in plant in a Zn-deficient Cd-contaminated soil. Although, health risk index (HRI) from the soil sampling area seems to be lower than <1 for Cd but may exceed due to long-term consumption of grains produced from such contaminated soil. Foliar applied Zn-lys reduced HRI which may help to reduce health risks associated with Cd.

Human health implications, risk assessment and remediation of As-contaminated water: A critical review.

Arsenic (As) is a naturally occurring metalloid and Class-A human carcinogen. Exposure to As via direct intake of As-contaminated water or ingestion of As-contaminated edible crops is considered a life threatening problem around the globe. Arsenic-laced drinking water has affected the lives of over 200 million people in 105 countries worldwide. Limited data are available on various health risk assessment models/frameworks used to predict carcinogenic and non-carcinogenic health effects caused by As-contaminated water. Therefore, this discussion highlights the need for future research focusing on human health risk assessment of individual As species (both organic and inorganic) present in As-contaminated water. Various conventional and latest technologies for remediation of As-contaminated water are also reviewed along with a discussion of the fate of As-loaded waste and sludge.

Phosphate-assisted phytoremediation of arsenic by Brassica napus and Brassica juncea: Morphological and physiological response.

In this study, we examined the potential role of phosphate (P; 0, 50, 100 mg kg-1) on growth, gas exchange attributes, and photosynthetic pigments of Brassica napus and Brassica juncea under arsenic (As) stress (0, 25, 50, 75 mg kg-1) in a pot experiment. Results revealed that phosphate supplementation (P100) to As-stressed plants significantly increased shoot As concentration, dry biomass yield, and As uptake, in addition to the improved morphological and gas exchange attributes and photosynthetic pigments over P0. However, phosphate-assisted increase in As uptake was substantially (up to two times) greater for B. napus, notably due to higher shoot As concentration and dry biomass yield, compared to B. juncea at the P100 level. While phosphate addition in soil (P100) led to enhanced shoot As concentration in B. juncea, it reduced shoot dry biomass, primarily after 50 and 75 mg kg-1 As treatments. The translocation factor and bioconcentration factor values of B. napus were higher than B. juncea for all As levels in the presence of phosphate. This study demonstrates that phosphate supplementation has a potential to improve As phytoextraction efficiency, predominantly for B. napus, by minimizing As-induced damage to plant growth, as well as by improving the physiological and photosynthetic attributes.