Assessment of plant ecological variability and heavy metal accumulation potential in naturally growing plant species of Pakhar bauxite mine site, Jharkhand, India.

Abandoned bauxite mine (ABM) soil generally contains an unacceptable number of heavy metals (HMs), causing several ecological and environmental issues. The present study was conducted with a similar objective to assess the HM accumulation potential of the naturally growing plant species from Pakhar ABM site. Vegetation communities were studied using quadrat methods for plant species at both ABM and the control site (near the ABM site). A total of 21 (9 at the ABM site and 12 at the control site) plant species were recorded in the present study belonging to 10 families. Vegetation study revealed that the dominant plant species were Ammophila arenaria and Lantana camara at ABM site and Lantana camara at the control site. The concentration of HMs in soil at the ABM site, were 66180.00 mg kg-1 Al, 62.20 mg kg-1 Cr, 22.60 mg kg-1 Cu, 346800.00 mg kg-1 Fe, 780.80 mg kg-1 Mn, and 39.80 mg kg-1 Zn while in the soil of site located nearby taken as the control showed 56500.00 mg kg-1 Al, 4.40 mg kg-1 Cu, 51120.00 mg kg-1 Fe, 58.20 mg kg-1 Mn, 13.00 mg kg-1 Zn. Ammophila arenaria, Miscanthus sinensis, Acacia drepanolobium and Rumex pulcher exhibited the highest metal accumulation at the ABM site, while Ocimum campechianum, Lantana camara, Panicum virgatum L., Euphorbia hirta and Holcus lanatus, Cerastium glomeratum thuill and Shorea robusta exhibited the highest metal accumulation at control site. Plant Lantana camara showed considerable TF values for Pb, Al and Fe, from the ABM soil while Shorea robusta showed high TF values for Al, Cu, Zn, and Fe from the control soil. The BAF for Cu, Mn and Zn from ABM soil were observed in Acacia drepanolobium whereas Cerastium glomeratum thuill exhibited maximum BAF values for Zn and Cu from control soil.

Potential transmission of SARS-CoV-2 through microplastics in sewage: A wastewater-based epidemiological review.

In light of the current COVID-19 pandemic caused by the virus SARS-CoV-2, there is an urgent need to identify and investigate the various pathways of transmission. In addition to contact and aerosol transmission of the virus, this review investigated the possibility of its transmission via microplastics found in sewage. Wastewater-based epidemiological studies on the virus have confirmed its presence and persistence in both influent sewage as well as treated ones. The hypothesis behind the study is that the huge amount of microplastics, especially Polyvinyl Chloride and Polyethylene particles released into the open waters from sewage can become a good substrate and vector for microbes, especially Polyvinyl Chloride and Polyethylene particles, imparting stability to microbes and aiding the "plastisphere" formation. A bibliometric analysis highlights the negligence of research toward plastispheres and their presence in sewage. The ubiquity of microplastics and their release along with the virus into the open waters increases the risk of viral plastispheres. These plastispheres may be ingested by aquatic organisms facilitating reverse zoonosis and the commercial organisms already reported with accumulating microplastics through the food chain poses a risk to human populations as well. Reliance of high population density areas on open waters served by untreated sewage in economically less developed countries might bring back viral transmission.

Environmental Application of Graphene and Its Forms for Wastewater Treatment: a Sustainable Solution Toward Improved Public Health.

Public health is seriously jeopardized in developing countries due to poor sanitation and the presence of persistent pollutants in natural water bodies. Open dumping, wastewater discharge without proper treatment and atmospheric fallout of the organic and inorganic pollutants are the main causes behind the poor condition. Some of the pollutants pose a greater risk due to their toxicity and persistence. Such a class of pollutants are known as chemical contaminants of emerging concern (CECC), including antibiotics and drug residues, endocrine disruptors, pesticides and micro- and nano-plastics. Conventional treatment methods cannot treat them properly and are often associated with several disadvantages. However, the chronological development of techniques and materials for their treatment has exhibited graphene as an efficient candidate for environmental remediation. This current review considers the various graphene-based materials, their properties, advancement in synthesis methods with time and their detailed application in removing dyes, antibiotics and heavy metals. It has been discussed how graphene and its derivatives exhibit unique electronic, mechanical, structural and thermal properties. In this paper, the mechanism of adsorption and degradation using these graphene-based materials has also been discussed vividly. In addition to this, a bibliographic analysis was performed to identify the trend of research related to graphene and its derivatives in the adsorption and degradation of pollutants round the globe reflected by the publications. Therefore, this review can be instrumental in understanding the fact that further development of graphene-based materials and their mass production can provide a very effective and economical wastewater treatment method.

A state-of-the-art review on cadmium uptake, toxicity, and tolerance in rice: From physiological response to remediation process.

Cadmium (Cd), a major contaminant of concern, has been extensively reviewed and debated for its anthropogenic global shifts. Cadmium levels in rice grains raise wide food safety concerns. The aim of this review is therefore to capture the dynamics of Cd in paddy soil, translocation pathways of Cd from soil to consumption rice, and assess its bio-accessibility in human consumption. In crop plants, Cd reduces absorption of nutrients and water, triggers oxidative stress, and inhibits plant metabolism. Understanding the mechanisms and behaviour of Cd in paddy soil and rice allows to explain, predict and intervene in Cd transferability from soil to grains and human exposure. Factors affecting Cd movement in soil, and further to rice grain, are elucidated. Recently, physiological and molecular understanding of Cd transport in rice plants have been advanced. Morphological-biochemical characteristics and Cd transporters of plants in such a movement were also highlighted. Ecologically viable remediation approaches, including low input cost agronomic methods, phytoremediation and microbial bioremediation methods, are emerging.

Removal of toxic dye from dye-laden wastewater using a new nanocomposite material: Isotherm, kinetics and adsorption mechanism.

In this study, (hemi)cellulosic biochar-based environment-friendly non-toxic nanocomposite (nAg-AC) was fabricated for an inordinate overlook of toxic dye-laden wastewater depollution. This hybrid nanocomposite grafted with silver nanoparticles, numerous hydroxyl and π-bond containing functional groups exhibited outstanding physicochemical properties. FESEM images indicated the heterogeneous porous structure of nAg-AC, while BET analysis revealed mesoporous property with a significant increment of overall surface area (132%). Imbedding of silver nanoparticles and the presence of multiple hydroxyl groups was evident from the XRD and XPS spectrum. Further, the TGA result indicated excellent thermal stability, and FTIR analysis suggested the involvement of surface functional groups like -OH, =C = O, =NH, =C = C = , and -CH in Rhodamine B (RhB) adsorption. The adsorbent matrix provided the overall mechanical strength and facilitated recycling, while the functional matrix (biochar) provided the adsorptive locus for augmented RhB adsorption efficiency (92.77%). Experiments pertaining to adsorption isotherms and kinetics modeling suggested that RhB was removed through multilayer chemisorption on the heterogeneous nAg-AC surface. The main RhB adsorption mechanism included cumulative efforts of H-bindings, π-π stacking interaction, pore-filling, and electrostatic interactions. The nAg-AC maintained mechanical robustness with significant RhB adsorption even after three consecutive regeneration cycles signifying facile recycling. The nAg-AC displayed an outstanding efficacy for the real industrial wastewater depollution, indicating high effectiveness for practical environmental applications. Finally, the cost analysis (incorporating economic, environmental, and social dimensions) suggested a significant role of the nAg-AC in promoting and establishing sustainable development with the circular economy.

Valorization of fruit waste-based biochar for arsenic removal in soils.

Fruit waste disposal is a serious global problem with only 20% of such waste being routinely treated prior to discharge. Two of the most polluting fruit wastes are orange peel and walnut shell and new methods are urgently required to valorize such waste. In the present study, they where valorized via conversion into biochars at 500 °C (OPB500 for orange peel-based biochar produced at 500 °C and WaSB500 for walnut shell-based biochar produced at 500 °C), and evaluated for arsenic adsorption. A pore-rich surface morphology was observed with a low H/C ratio indicating high stability. Spectroscopic studies revealed the presence of minerals and surface functional groups (amide, carbonyl, carboxyl, and hydroxyl) suggesting high potential for arsenic immobilization. Adsorption studies revealed an arsenic removal efficiency of 88.8 ± 0.04% for WaSB500 exposed to initial arsenic concentration of 8 ppm for 5% biochar dose at 25 °C and 30 min contact time. In comparison, OPB500 showed slightly lower removal efficiency of 80.7 ± 0.1% (10 ppm initial concentration, 5% dose, 25 °C, 90 min contact time). Peak shifts in XRD and FTIR spectra together with isotherm, kinetic, and thermodynamic studies suggested arsenic sequestration was achieved via a combination of chemisorption, physisorption, ion exchange, and diffusion. The present investigation suggests valorization of fruit waste into thermo-stable biochars for sustainable arsenic remediation in dynamic soil/water systems and establishes biochar's importance for waste biomass minimization and metal (loid) removal from fertile soils.

Fabrication of biochar-based hybrid Ag nanocomposite from algal biomass waste for toxic dye-laden wastewater treatment.

Dual functional innovative approaches were developed to tackle the algal scum problem in water by utilizing the algal (Spirogyra sp.) biomass waste for organic dye-laden industrial wastewater treatment, a global problem, and challenge. Therefore, an algal biochar-based nanocomposite (nAgBC) was synthesized and employed as a low-cost adsorbent for Congo red (CR) removal. Surface morphology, physicochemical characteristics, elemental composition, phase, and stability of the nanocomposite was analyzed using BET, FESEM-EDX, FTIR, XRD, XPS, and TGA. The nanocomposite was found to be thermostable, mesoporous with large and heterogeneous surface area, containing nAg as doped material, where -OH, NH, CO, CC, SO, and CH are the surface binding active functional groups. Maximum adsorption efficiency of 95.92% (18 mg L-1 CR) was achieved (qe = 34.53 mg g-1) with 0.5 g L-1 of nanocomposite after 60 min, at room temperature (300 K) at pH 6. Isotherm and kinetic model suggested multilayer chemisorption, where adsorption thermodynamics indicated spontaneous reaction. Fluorescens spectral analysis of CR confirmed the formation of CR supramolecule, supporting enhanced adsorption. Furthermore, the result suggested a 5th cycle reusability and considerable efficacy towards real textile industrial effluents. Synergistic effects of the active surface functional groups of the biochar and nAg, along with the overall surface charge of the composite lead to chemisorption, electrostatic attraction, H-bonding, and surface complexation with CR molecules. Thus, synthesized nAgBC can be applicable to mitigate the wastewater for cleaner production and environment.

Biochar-based nanocomposite from waste tea leaf for toxic dye removal: From facile fabrication to functional fitness.

The present study utilized discarded tea leaf waste to produce 'Tea leaf biochar' (TLB) as the functional matrix for the fabrication of hybrid nanocomposite (nAg-TC), with colloidal deposition of silver nanoparticles (nAg) via modified chemical co-precipitation, for treatment of dye-laden wastewater. The chemical composition, physicochemical properties, and morphology of nAg-TC, and active surface functional groups involved in adsorption were identified using BET, FESEM-EDX, FTIR, TGA, XPS, and XRD. The nAg-TC matrix was found to be heterogeneous, mesoporous, thermostable, with rich in active surface functional groups (-OH, =NH, =CH, CC, CO, CN, and CC), and nAg as a dopant material. The dye adsorption results indicated the maximum removal efficiency (RhB = 95.89%, CR = 94.10%) at 300 K for rhodamine B (RhB) and Congo red (CR) concentrations of 25 mg L-1 and 22.5 mg L-1, respectively. The present investigation agreed with Freundlich isotherm (R2CR:0.991; R2RhB:0.993) and pseudo-second order kinetic (R2CR:0.999; R2RhB:0.999) model, indicating overall adsorption of RhB and CR through spontaneous and exothermic chemisorption on the heterogeneous surface of nAg-TC. The mechanism of RhB and CR adsorption was complex where nAg-TC, possessing the synergistic effects of TLB and nAg, showed surface complexation, electrostatic attraction, and H-bonding, leading to chemisorption. Study showed excellent reusability of spent nAg-TC, and commendable treatment efficiency for dye-laden real industrial effluents. The study exhibits substantial techno-economic feasibility of adsorbent and translates the principles of circular economy into synthesis of value-added products through sustainable management of biowaste and bioresource.

A review of the phytochemical mediated synthesis of AgNP (silver nanoparticle): the wonder particle of the past decade.

Silver nanoparticle (AgNP) has been one of the most commonly used nanoparticles since the past decade for a wide range of applications, including environmental, agricultural, and medical fields, due to their unique physicochemical properties and ease of synthesis. Though chemical and physical methods of fabricating AgNPs have been quite popular, they posed various environmental problems. As a result, the bioinspired route of AgNP synthesis emerged as the preferred pathway for synthesis. This review focuses extensively on the biosynthesis of AgNP-mediated through different plant species worldwide in the past 10 years. The most popularly utilized application areas have been highlighted with their in-depth mechanistic approach in this review, along with the discussion on the different phytochemicals playing an important role in the bio-reduction of silver ions. In addition to this, the environmental factors which govern their synthesis and stability have been reviewed. The paper systematically analyses the trend of research on AgNP biosynthesis throughout the world through bibliometric analysis. Apart from this, the feasibility analysis of the plant-mediated synthesis of nanoparticles and their applications have been intrigued considering the perspectives of engineering, economic, and environmental limitations. Thus, the review is not only a comprehensive summary of the achievements and current status of plant-mediated biosynthesis but also provides insight into emerging future research frontier. Supplementary Information: The online version contains supplementary material available at 10.1007/s13204-021-02135-5.

Photocatalytic degradation of Congo Red under UV irradiation by zero valent iron nano particles (nZVI) synthesized using Shorea robusta (Sal) leaf extract.

In the present study, photo catalytic degradation of azo dye Congo Red was conducted using Fe nano particles (nZVI) in the presence of UV light. nZVI was biosynthesized using FeSO4.7H2O precursor and leaf extract of Shorea robusta (sal) as reducing agent under optimum condition of 1 mM concentration of precursor and a ratio of 1:1 Sal leaf extract to precursor. TEM and AFM images revealed formation of well dispersed spherical nano particles of 54-80 nm. SAED patterns of nZVI particles indicated its crystalline nature, while EDX result showed the presence of iron as the most abundant element. In batch experiments, optimum degradation of CR was 96% at 220 ppm CR with a dose of 1.2 g/L nZVI at pH 4 in 15 min following pseudo second order kinetics. The study suggested nZVI to be a potentially economic and ecofriendly technique for treatment of Congo Red.

Synthesis of silver nanoparticle with Colocasia esculenta (L.) stem and its larvicidal activity against Culex quinquefasciatus and Chironomus sp

Objective: To synthesize silver nanoparticles with Colocasia esculenta as a reducing agent and to evaluate their effect against Culex quinquefasciatus and Chironomus sp. Methods: The aqueous extract of Colocasia esculenta stem was used for nanosynthesis. The synthesized nanoparticles were characterized by UV-Vis spectrophotometry, Fourier-transform infrared spectroscopy, scanning electron microscope, transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction and Zeta potential studies. The toxicity of Colocasia esculenta stem extract and the synthesized silver nanoparticles was evaluated against the larval stages of target human filarial vector Culex quinquefasciatus and non-target Chironomus sp. Results: Scanning electron microscopy and transmission electron microscopy studies revealed almost spherical shape of the synthesized silver nanoparticles with size ranging from 13-50 nm. After 24 hours of exposure, the LC50 and LC90 of the plant extract against 4th instars larvae of Culex quinquefasciatus were 745.56 mg/L and 1258.28 mg/L, respectively, which were higher than those of synthesized silver nanoparticles (5.17 mg/L and 17.32 mg/L after 24 h; 1.58 mg/L and 13.01 mg/L after 48 h). In addition, the LC50 and LC90 of silver nanoparticles against Chironomus sp. were 9.71 mg/L and 23.15 mg/L after 24 h as well as 2.38 mg/L and 19.49 mg/ L after 48 h, respectively. Conclusions: The aqueous stem extract of Colocasia esculenta is a good agent for synthesis of silver nanoparticles, which are almost spherical with size less than 30 nm. The synthesized nanoparticles show good larvicidal activity without any harmful effect on non-target species.

Metal phytoremediation potential of naturally growing plants on fly ash dumpsite of Patratu thermal power station, Jharkhand, India.

Three naturally growing plants Ipomoea carnea, Lantana camara, and Solanum surattense were found in fly ash dumpsite of Patratu thermal power station, Jharkhand, India. They were assessed for their metal uptake potential. The fly ash was slightly alkaline with very less nitrogen and organic carbon but enriched with phosphorus and heavy metals. Lantana camara and Ipomoea carnea showed good translocation from root to shoot for most of the metals except Mn and Pb. The order of metal accumulation in stem of both the plants were Fe(205mg/kg)>Mn(65mg/kg)>Cu(22.35mg/kg)>Pb(6.6mg/kg)>Cr(3.05mg/kg)>Ni(1 mg/kg)>Cd(0.5 mg/kg) and Fe(741 mg/kg)>Mn(154.05 mg/kg)>Cu(20.75 mg/kg)>Pb(6.75 mg/kg)>Ni(4.0 mg/kg)>Cr(3.3mg/kg)>Cd(0.05mg/kg), respectively. But Solanum surattense accumulated most of the metals in roots. The order was in the following order, Mn (382.2mg/kg) >Fe (264.1mg/kg) > Cu (25.35mg/kg) >Pb (5.95 mg/kg) > Ni (1.9 mg/kg) > Cr (1.8mg/kg) > Cd (0.55 mg/kg). The order of Bioconcentration factor (BCF) in root and shoot followed almost the same order as, Mn>Fe>Ni>Pb>Cu>Cr≈ Cd in all the three species. ANOVA showed significant variation in metal accumulation by root and stem between the species. Finally, it can be concluded that Solanum surattense can be used as phytostabilizer and other two species as phytoextractor of metal for fly ash dumpsite reclamation.

Benthic macroalgae as biological indicators of heavy metal pollution in the marine environments: a biomonitoring approach for pollution assessment.

Metal pollution in the marine coastline environment is an important topical issue in the context of ecological disturbance and climate change. Heavy metal contaminations (Cd, Cr, Cu, Mn, Ni, Pb and Zn) in seawater and surficial sediments, as well as macroalgal diversity, were determined in six different locations along the coast of the Gulf of Kutch in India. The marine coastline environment was found to be enriched with Cd and Zn in comparison to other metals. Significant (p ≤ 0.05) inter-elemental positive-correlations were observed between Fe-Mn, Fe-Cu, Fe-Cr, Fe-Zn, Cr-Cu, Cu-Mn, and Cd-Zn, as well as negative-correlations between Cd-Pb, Ni-Pb, and Zn-Pb. Though genus specific macroalgal responses to heavy metal accumulation were significant, species specific response was insignificant (p ≤ 0.05). The relative abundance of metals in macroalgae followed the order of Fe>Zn>Mn>Cu>Cd>Cr>Ni>Pb. The high uptake of metals in green algae (Ulva lactuca and Enteromorpha intestinalis) and brown algae (Padina gymnospora and Dictyota bartayresiana) suggested that these algae may be used as potential biomonitors for heavy metal pollution. Three pollution indicators, Contamination Factor (CF), Enrichment Factor (EF) and Geochemical Index (Igeo) were calculated to determine the degree of metal pollution in the marine coastline and the contribution of anthropogenic influence.

Depth-resolved abundance and diversity of arsenite-oxidizing bacteria in the groundwater of Beimen, a blackfoot disease endemic area of southwestern Taiwan.

The role of arsenite oxidizers in natural attenuation of arsenic pollution necessitates studies on their abundance and diversity in arsenic-contaminated aquifers. In this study, most probable number-polymerase chain reaction (MPN-PCR) and denaturing gradient gel electrophoresis (DGGE) was applied to monitor depth-wise abundance and diversity of aerobic arsenite oxidizers in arsenic-enriched groundwater of Beimen, southwestern Taiwan. The results revealed that the abundance of arsenite oxidizers ranged from 0.04 to 0.22, and the lowest ratio was observed in the most arsenic-enriched and comparatively more reduced groundwater (depth 200 m) of Beimen 1. The highest ratio was observed in the less arsenic-enriched and less reduced groundwater (depth 60 m) of Beimen 2B. DGGE profiles showed a shift in diversity of arsenite oxidizers, consisting of members of the Betaproteobacteria (61%), Alphaproteobacteria (28%) and Gammaproteobacteria (11%), depending on mainly arsenic concentration and redox level in groundwater. Groundwater with the lowest arsenic and highest dissolved oxygen at Beimen 2B harbored 78% of the arsenite oxidizers communities, while groundwater with the highest arsenic and lowest dissolved oxygen at Beimen 1 and Beimen-Jinhu harbored 17 and 22% of arsenite oxidizers communities, respectively. Pseudomonas sp. was found only in groundwater containing high arsenic at Beimen 1 and Beimen-Jinhu, while arsenite oxidizers belonging to Alpha- and Betaproteobacteria were dominated in groundwater containing low arsenic.