Plant–soil interactions have bottom–up and top–down effects within a plant community. Heavy metal pollution can change plant–soil interactions, directly influence bottom–up effects and indirectly affect herbivores within the community. In turn, herbivores can affect plant–soil interactions through top–down effects. However, the combined effects of heavy metals and herbivores on soil enzymes, plants and herbivores have rarely been reported. Therefore, the effects of lead (Pb), Spodoptera litura and their combined effects on soil enzyme activities, pakchoi nutrition, defence compounds and S. litura fitness were examined here. Results showed that Pb, S. litura and their combined effects significantly affected soil enzymes, pakchoi and S. litura. Specifically, exposure to double stress (Pb and S. litura) decreased soil urease, phosphatase and sucrase activities compared with controls. Furthermore, the soluble protein and sugar contents of pakchoi decreased, and the trypsin inhibitor content and antioxidant enzyme activity increased. Finally, the S. litura development period was extended, and survival, emergence rates and body weight decreased after exposure to double stress. The combined stress of Pb and S. litura significantly decreased soil enzyme activities. Heavy metal accumulation in plants may create a superposition or synergistic effect with heavy metal-mediated plant chemical defence, further suppressing herbivore development. Pb, S. litura and their combined effects inhibited soil enzyme activities, improved pakchoi resistance and reduced S. litura development. The results reveal details of soil–plant–herbivore interactions and provide a reference for crop pest control management in the presence of heavy metal pollution.

The ability of Na-activated bentonite to remove Ni2+ and Co2+ from aqueous solutions at room temperature (22 ± 1°C) was studied under various experimental conditions. The parameters studied were solid-to-liquid ratios and initial cation concentrations. Experiments involved the behavior of bentonite vs. Ni and Co separately and where Ni and Co were present in solution at different concentrations and ratios. Bentonite retained substantial amounts of both metals readily, but it showed a higher affinity for Ni. Over-exchange appears when initial metal concentration exceeds the concentration corresponding to the cation exchange capacity (CEC) of bentonite. The presence of both metals in solution may be either synergistic or antagonistic sorption, depending on the initial ion concentrations.

This paper examines the ion-exchange properties of synthetic zeolite Na-Pc, which was produced from perlite-waste fines and has a SiO2:Al2O3 ratio of 4.45:1 and a cation-exchange capacity (CEC) of 3.95 meq g−1. Although equilibrium is attained rapidly for all three metals, exchange is incomplete, with Ac(max) (maximum equilibrium fraction of the metal in the zeolite) being 0.95 for Pb, 0.76 for Zn, and 0.27 for Ni. In both Na → ½Pb and Na → ½Zn exchange, the normalized selectivity coefficient is virtually constant for NAC (normalized equilibrium fraction of the metal in the zeolite) values of ≤0.6, suggesting a pronounced homogeneity of the available exchange sites. The Gibbs standard free energy, ΔG°, of the Na → ½Pb exchange calculated from the normalized selectivity coefficient is −3.11 kJ eq−1 and, for the Na → ½Zn exchange, it is 2.75 kJ eq−1.

Examination of the solid exchange products with X-ray diffraction (XRD) revealed a possible decrease in crystallinity of zeolite Pb-Pc as suggested by the significant broadening and disappearance of diffraction lines. This decrease is associated with a reduction of pore opening, as indicated from Fourier-transform infrared analysis (FTIR), which in turn results in a decrease of the amount of zeolitic water. Thermogra-vimetric-differential thermogravimetric (TG-DTG) analysis showed that water loss occurs in three steps, the relative significance of which depends on the type of exchangeable cation and subsequently on the type of complex formed with the cation and/or the zeolite channels. Zeolite Na-Pc might be utilized in environmental applications, such as the treatment of acid-mine drainage and electroplating effluents.

The sorption of Cd, Cu, Pb, and Zn ions by Na-rich bentonite, Al and Zr-pillared Na-rich bentonite (Al-MX80, Zr-MX80), the uncalcined hydroxy-intercalated precursors (HAl, HZr-MX80), and commercial Al-pillared bentonite EXM 534 was investigated. Experiments were conducted in ultrapure water and artificial leachate with varying pH. The experiments were performed over periods to 30 wk. Sorption characteristics were described with one and two-site Langmuir isotherms. The non-exchangeable quantities of heavy metals were determined by fusion of the sorbents after ion exchange with ammonium acetate.

The sorption of Cd, Cu, Pb, and Zn by bentonite was dominated by cation exchange. In artificial leachate, the sorption was reduced due to competition with alkali and alkaline-earth cations. The sorption of Cu, Zn, and Pb at pH 4.9 and Cd at pH 6.9 by Al and Zr-hydroxy-intercalated and pillared MX80 was governed also by cation exchange. In contrast, the sorbed quantities of Zn at pH 6.9 exceeded the cation exchange capacity (CEC) of HAl, HZr, Al, Zr-MX80, and EXM 534 and were partially non-exchangeable. The increase of the sorption of Zn with pH and its independence of the ionic strength of the solution at neutral pH suggest a complexation of Zn ions to surface hydroxyl groups of the intercalated Al and Zr-polyhydroxo cations and pillars. This complexation is the dominating sorption mechanism. Removal of dissolved Zn from solution with time is attributed to surface precipitation. Al-hydroxy and pillared bentonites are considered potential sorbents of Zn ions from neutral pH aqueous solutions, such as waste waters and leachates.

A synergistic mechanism for the retention of organic and inorganic pollutants in clays is discussed in this paper. The mechanism of adsorption of cis- or trans- 1,2-dichloroethylene vapor (CDE or TDE, respectively) by hydrated smectite clay (hectorite) exchanged with Pb2+, Hg2+, Cd2+, Ca2+, Ag+, or Na+ has been investigated by simultaneously measuring chlorohydrocarbon uptake and water desorption isotherm and by recording the infrared (IR) spectrum of the adsorbed phase. Hydrated hectorite saturated with divalent cations adsorbs about 55% more CDE or 35% more TDE than those saturated with monovalent cations. The quantity of chlorohydrocarbon adsorbed is also a function of the hydration of the clay interlayer space. When dehydrated, hectorite does not adsorb CDE or TDE. Upon long outgassing at room temperature or even at 100°C, the characteristic IR bands of clays with adsorbed chlorohydrocarbon, although much weakened, are still observable. The ratio of the amount of water desorbed to the amount of chlorohydrocarbon adsorbed varied from about 0.22 to 0.34. A shift of the center of gravity of the hydration water OH stretching frequency towards a higher wavenumber and of the asymmetric CC1 stretching vibration toward a lower frequency suggest that the formation of hydrogen bonds between CDE or TDE and water is the driving force for adsorption and that the cation-dipole interaction does not play a major role.

Batch sorption studies of Cr(III), Ni(II), Zn(II), Cu(II) and Cd(II) were conducted on Ca-bentonite and Na-bentonite to determine their retention capacities for these metal cations commonly present in the waste waters of galvanic industries. The Langmuir model was found to describe the sorption process well, offering maximum sorption capacities of 44.4 mg Cr/g, 6.32 mg Ni/g, 5.75 mg Zn/g, 7.72 mg Cu/g, 7.28 mg Cd/g on Ca-bentonite and 49.8 mg Cr/g, 24.2 mg Ni/g, 23.1 mg Zn/g, 30.0 mg Cu/g, 26.2 mg Cd/g on Na-bentonite. The use of Na-bentonite in the purification of waste waters from Ni, Cr and acid-Zn electroplating processes was an effective treatment in small-scale and in semi-industrial-scale tests. This proves the worth of this method as an alternative to existing methods. In contrast, Nabentonite was not effective in Zn sorption from cyanide-containing waste waters.

Because long-term leachate migration through a hydraulic barrier is inevitable, compacted clay and cementitious liners are commonly used as ‘active-passive’ liners to attenuate percolated leachate. The scarcity of suitable clay and because of the CO2 emitted during the production of Portland cement as well as drying shrinkage, flow rate due to consolidation, limited attenuation capacity, and chemical instability may mean that these are not the best choices of materials to use for this purpose. An environmentally friendly method to improve the properties of local clay and provision for a long-term physical and chemical containment are essential. Geopolymers can be environmentally friendly substitutes for Portland cement to improve soil properties, not just because of the reduced carbon dioxide emission, but also because of its superior physical and chemical properties, as well as significant early strength, reduced shrinkage, freeze-thaw resistance, long-term durability, and attenuation capacity. According to previous studies, class-F fly ash-based geopolymers activated with NaOH exhibit superior attenuation capacity and long-term durability. The presence of silica, alumina, and iron oxides and the lack of calcium oxide play pivotal roles in the acceptable attenuation capacity and chemical stability of class-F fly ash. Accordingly, a clay-fly ash geopolymer may also work as a sustainable liner with appropriate physical and chemical performance. Clay can also participate in the geopolymerization process as an alumino-silicate precursor. All components of clay-fly ash geopolymers possess acceptable adsorption capacity. The type and percentage of the constituent raw materials control the attenuation capacity and physical properties of final products, however. The porosity and conductivity of typical geopolymers are related to the activator type and concentration, water content, and curing condition. Furthermore, the properties of liner materials can be adjusted with respect to the target contaminants. The present study aimed to present a comprehensive review of the relevant studies to highlight the properties required.

Enzymes adsorbed on clay minerals and soil colloids may exhibit lower activities compared to those of free enzymes. A particular toxic metal may affect the activity of the adsorbed enzyme less critically than that of the free form, however. This information is necessary for predicting catalytic performances of clay-immobilized enzymes in natural soils as well as in food, pharmaceutical, and chemical systems. The objective of the present study was to find out how adsorption on palygorskite and sepiolite minerals modifies the catalytic activity and the Michaelis–Menten kinetics of alkaline phosphatase (ALP). Inhibition kinetics of adsorbed ALP by Cd was also compared to that of the free enzyme. The results revealed that the affinity to the substrate and the maximum reaction velocity of ALP decreased upon adsorption on the fibrous clay minerals. The ALP adsorbed maintained a reasonably high activity recovery (AR) compared to the free enzyme. The AR of the adsorbed ALP ranged from 76.9 to 92.5% for palygorskite and from 71.2 to 90.2% for sepiolite, depending on the substrate concentration applied. The presence of Cd decreased the affinity to the substrate of both the free and the adsorbed ALP, while the maximum reaction velocity remained nearly unchanged, indicating that the inhibitory effects of Cd on both the free and adsorbed ALP activities were competitive in nature. The adsorbed enzyme, however, was inhibited less severely by Cd compared to the free enzyme. The adsorption of ALP on the fibrous clay minerals, therefore, maintains the ALP activity to a great extent and provides more resistance for the enzyme against the inhibitory effects of Cd.

Immunological and oxidative alterations have been reported around calving in dairy cattle. In addition, the levels of heavy metals rise in the blood around parturition, which might affect body systems. Therefore, in this Research Communication we evaluate the changes in whole blood lead (Pb), arsenic (As), and cadmium (Cd) around calving, in comparison with the beginning of the dry period, and assess the correlations of these elements with immunological factors and oxidative markers. Samples were collected from 30 clinically healthy dairy cows in the early dry period (−6 w), one week before expected calving (−1 w), and one week postpartum (+1 w). The highest concentrations of Pb, As, and Cd were observed at −1 w and all the three elements decreased after parturition leading to significantly lower As and Cd, compared to −1 w (P < 0.05). The lowest levels of tumor necrosis factor-alpha, immunoglobulin G, interleukin 4, interleukin 10 and haptoglobin were found at −1 w simultaneous with the highest measures of the heavy metals, with tumor necrosis factor-alpha being significantly lower at this time (P < 0.05). At −6 w, As concentration was significantly (P < 0.05) correlated negatively (r = −0.366) and positively (r = 0.417) with total antioxidant capacity and malondialdehyde, respectively. Furthermore, at −1 w Pb and As had significant (P < 0.05) negative correlations with interferon gamma (r = −0.502) and interleukin 4 (r = −0.483), respectively. After parturition, Pb was observed to be negatively correlated with total antioxidant capacity (r = −0.538, P < 0.05). The observed results revealed that the alterations in immunological factors and antioxidant capacity around parturition were correlated with Pb and As levels.

Composting from organic municipal solid waste (MSW), such as a separate waste collection, is a valid tool for eliminating a considerable amount of waste that would otherwise be destined for landfills and incinerators, thus representing an effective complement to traditional forms of recycling. It allows organic substance to be recovered and reintegrated into the soil, thus preventing erosion phenomena, increasing the biological fertility of the soil and contributing significantly to the restoration of impoverished sites. Modern winegrowing must address the issue of vineyard fertility in the sustainability context. The goal of this study was to assess the advantages of distributing a sustainable product to the vineyard that can achieve vine balance (vegetative and productive equilibrium). In a Vitis vinifera L. Sangiovese cv., vineyard, four soil treatments were applied (three compost rates and a control): municipal solid waste compost (40 tons per hectare – MSW40, 15 tons per hectare – MSW15, 2.5 tons per hectare – MSW2.5), and no compost (CTRL). The vine physiology (leaf gas exchange and water potential) and berry compositions (phenolic and technological maturity) were studied during the 2018–2019 growing seasons in the Sieci area, Italy. The results of this experiment provide some general insights showing that MSW compost options can be expected to reduce water stress, balanced vine performance and provide sustainable recirculation of organic matter. MSW compost is a true agronomic and environmental resource.

The treatment of water containing heavy metals has attracted increasing attention because the ingestion of such water poses risks to human health. Due to their relatively large specific surface areas and surface charges, clay minerals play a significant role in the adsorption of heavy metals in water. However, the major factors that influence the adsorption rates of clay minerals are not well understood, and thus methods to predict the sorption of heavy metals by clay minerals are lacking. A method that can identify the most appropriate clay minerals for removal of a given heavy metal, based on the predicted sorption of the clay minerals, is required. This paper presents a widely applicable deep learning neural network approach that yielded excellent predictions of the influence of the sorption ratio on the adsorption of heavy metals by clay minerals. The neural network model was based on datasets of heavy-metal parameters that are available generally. It yielded highly accurate predictions of the adsorption rate based on training data from the dataset and was able to account for a wide range of input parameters. A Pearson sensitivity analysis was used to determine the contributions of individual input parameters to the adsorption rates predicted by the neural network. This newly developed method can predict the major factors influencing heavy-metal adsorption rates. The model described here could be applied in a wide range of scenarios.

Vegetables are widely cultivated in high rainfall and mountainous regions in Sri Lanka with poor soil conservation practices. Accumulation of essential mineral and toxic trace elements in the soils and widely cultivated vegetables of this region are poorly understood. One hundred soil and vegetable (i.e. cabbage, carrot and potato) samples were collected at the time of harvest and analysed for element concentrations. Soils contained high concentrations of essential mineral (N, P, K, Cu, Zn and Mn) and toxic trace elements (As, Cd and Pb). When comparing edible parts, cabbage contained the highest concentrations of mineral and toxic trace elements, and potato contained the lowest. Irrespective of the crop, edible parts contained high concentrations of N, P, K (14–35, 2–6, 15–24 g/kg, respectively), and Cu, Zn, Mn (2.5–6.7, 11–30, 8–147 mg/kg, respectively). Vegetables also contained As, Cd and Pb (0.04–1, 0.02–0.15, 0.02–0.26 mg/kg, respectively), but did not exceed the maximum permissible limits. Irrespective of the crop, 36–64 kg N, 6–11 kg P and 35–45 kg K per ha were removed with the harvest. According to the current rate of vegetable consumption by Sri Lankans (i.e. 240 g fresh weight (FW) per day), per capita consumption of 0.05–0.2 mg Cu, 0.45–0.65 mg Zn and 0.5–2 mg Mn per day through these vegetables was observed, i.e. 5–23% Cu, 7.5–11% Zn and 22–87% Mn of the recommended daily intake. Vegetables grown in the region served as a key source of essential mineral elements. However, agronomic mitigation strategies are needed to improve soil health and sustainability of these cropping systems.

Waterhyacinth [Eichhornia crassipes (Mart.) Solm] is an aquatic invasive plant that is widespread in Puerto Rico, where it negatively effects estuaries, freshwater wetlands, potable water reservoirs, and wildlife refuges. Specifically, the tropical estuary San Juan Bay Estuary (SJBE) has been impacted with the presence of E. crassipes. Infestations have led to a reduction of water circulation in the system and have facilitated the establishment of invasive fauna. Therefore, a field study was conducted in a cove between Laguna San Jose and Peninsula Cantera to assess the use of glyphosate and hand removal as a management tool for E. crassipes control. Aquatic macroinvertebrates and water quality were also monitored as a measure of environmental impact due to management activities. Results indicated that at 2 wk after glyphosate application, E. crassipes biomass (dry weight) was significantly reduced to 0.27 kg DW m−2 at the treated plot compared with the nontreated plot, which yielded 0.62 kg DW m−2. Fresh weight of E. crassipes decreased more than 90% when hand removal was used compared with glyphosate treatment. Dissolved oxygen and water pH were not significantly different between sites; however, water salinity increased to 8 to 9 ppt at both plots as a result of tidal activity. The order Hemiptera followed by Sarcoptiformes were common in the aquatic macroinvertebrate community. Macroinvertebrate species found associated with E. crassipes and considered natural enemies were: Orthogalumna terebrantis Wallwork, Niphograpta albigutalis (Warren), and Neochetina eichhorniae Warner. The use of glyphosate to manage E. crassipes at the Laguna San Jose was useful as a short-term control method, and its efficacy may be enhanced over time with follow-up applications in combination with hand removal.

Adsorption kinetic and thermodynamic tests were conducted using non-irradiated and γ-irradiated (400 kGy) NaOH-modified Philippine natural zeolites for the removal of Cu2+ ions in aqueous solution. The effects of γ-radiation on zeolites were investigated. Samples were equilibrated with binary systems of Cu2+ ↔ 2Na+ at room temperature. There were no significant changes in the elemental composition of the irradiated zeolite. Irradiation primarily results in the shrinking of the zeolite framework and improvements in the crystallinity. The γ-irradiation increases the sorption uptake according to the kinetic study in which the adsorption kinetics followed a pseudo-second-order model. Thermodynamic tests show that the adsorption isotherms of the two samples are best described by the Langmuir model. The maximum adsorption capacities of the non-irradiated and γ-irradiated NaOH-modified zeolites are 33.00 and 43.22 mg Cu2+ g–1, respectively, suggesting that γ-irradiation might enhance the maximum adsorption capacity by up to 30.8%.

Pollutant agents are exponentially increasing in modern society since industrialization processes and technology are being developed worldwide. Impact of pollution on public health is well known but little has been described on the association between environmental pollutants and mental health. A literature search on PubMed and EMBASE has been conducted and 134 articles published on the issue of pollution and mental health have been included, cited, reviewed, and summarized. Emerging evidences have been collected on association between major environmental pollutants (air pollutants, heavy metals, ionizing radiation [IR], organophosphate pesticides, light pollution, noise pollution, environmental catastrophes) and various mental health disorders including anxiety, mood, and psychotic syndromes. Underlying pathogenesis includes direct and indirect effects of these agents on brain, respectively, due to their biological effect on human Central Nervous System or related to some levels of stress generated by the exposure to the pollutant agents over the time. Most of emerging evidences are still nonconclusive. Further studies should clarify how industrial production, the exploitation of certain resources, the proximity to waste and energy residues, noise, and the change in lifestyles are connected with psychological distress and mental health problems for the affected populations.

Finding insect meals as alternative sources of poultry feedstuffs is a recent research topic; therefore, the present study aimed to evaluate the effects of defatted black soldier fly (Hermetia illucens L., HI) larvae meal in broiler chicken diets on the carcass characteristics and meat quality parameters, proximate composition, fatty acid profile and the heavy metal content of the breast meat. Four dietary treatments were designed: a control diet (HI0) and three experimental diets (HI5, HI10 and HI15), corresponding to 50, 100 and 150 g/kg HI inclusion levels, respectively. The inclusion of 50, 100 and 150 g HI meal per kg feed supply 16.56%, 33.01% and 49.63% of required crude protein. The broilers were slaughtered at day 35, the carcasses were weighed and the breast muscles were excised from 16 birds per each feeding group (two birds per replicate pens) and used for meat quality evaluation. Linear and quadratic responses were observed, for increasing HI meal levels, in the live and carcass weights (maximum for HI10). As far as the colour of the breast meat is concerned, redness (a*) showed a linear response, while yellowness (b*) linearly decreased with increasing HI meal levels (minimum for HI15). As the HI larvae meal increased in the diets, the moisture content linearly decreased and the protein content increased. The total saturated fatty acid and total monounsaturated fatty acid proportions rose to the detriment of the polyunsaturated fatty acid fraction. The HI larvae meal, used in the current study, represents a valuable protein source for broiler chickens when included by up to 100 g/kg in their diets, as an improved slaughtering performance was observed without any detrimental effects on meat quality parameters or heavy metal residues in the meat.

Marinobacter sp. W1-16 from Antarctic surface seawater was analysed for the production of extracellular polymeric substances (EPSs). Enhancement of the EPS biosynthesis was carried out by evaluating the influences of the carbon source (type and concentration), temperature, pH and salinity. EPS yields varied strongly depending on sugar substrate and temperature, while pH and salinity did not strongly affect levels of EPS production. Marinobacter sp. W1-16 produced the highest quantity of EPSs when growing at 15°C and pH 8, in the presence of 2% glucose and 3% NaCl. The EPS chemical characterization revealed a molecular weight of about 260 kDa. Colorimetric assays determined a higher quantity of carbohydrate than of proteins and uronic acids, as well as the presence of sulphate, in the extracted EPSs. The monosaccharidic composition resulted in Glc:Man:Gal:GalN:GalA:GlcA in relative molar proportions of 1:0.9:0.2:0.1:0.1:0.01. Some biotechnological potentialities (i.e. emulsifying and cryoprotective actions, and heavy metal binding properties) of the EPSs were proved, suggesting possible industrial and bioremediation applications.

In this study, we sought to evaluate the influence of cigarette smoke and pH cycling on the chemical composition and surface/cross-sectional enamel microhardness. A total of 40 dental blocks obtained from bovine incisors were divided into four groups (n=10): no treatment (control); exposure to cigarette smoke (CS); exposure to pH cycling (PC); and exposure to cigarette smoke and pH cycling (CS-PC). The samples were analyzed by synchrotron radiation micro X-ray fluorescence, bench mode X-ray fluorescence, as well as surface microhardness (SMH) and cross-sectional microhardness (CSMH) testing. The SMH results were submitted to analysis of variance (ANOVA) and Tukey’s test. The CSMH results were evaluated using split-plot ANOVA and Tukey’s test. A high amount of Cd and Pb and traces of Ni and As were observed in enamel and dentin after exposure to cigarette smoke (CS and CS-PC). The SMH and CSMH of CS were statistically higher when compared with the control. The PC and CS-PC showed lower SMH and CSMH. We conclude that exposure to cigarette smoke promoted heavy metal deposition in enamel/dentin. In addition, it increased the enamel microhardness but did not promote a protective effect on the in vitro development of caries. The clinical significance of this work is that there is significant bioaccumulation of heavy metals from cigarette smoke on the surface and in the enamel and dentin.