Dimethyl disulfide (DMDS) is a new soil fumigant that is considered a good alternative to methyl bromide due to its high activity toward soil-borne pests, with no ozone-depleting potential. The correlative literature for the study of DMDS and its environmental fate is limited. The hydrolysis kinetics of DMDS were studied in buffered aqueous solutions within a pH of 5, 7, and 9, temperature at 15, 25, 45, and 65 °C, and in natural water samples at an ambient temperature of 25 °C. The results showed that DMDS hydrolysis rates were accelerated by increases in pH and temperature. The calculated half-lives of DMDS hydrolysis in the solutions of pH 5, 7, and 9 were 13.91, 10.81, and 10.52 days, respectively at 25 °C, and the trend showed that DMDS hydrolyzed faster in neutral or mild alkali conditions than in acidic solutions at the same temperature. The calculated half-lives of DMDS hydrolysis in the solutions at 15, 25, 45, and 65 °C were 15.78, 10.81, 9.78, and 7.72 days at pH = 7, respectively. There existed no obvious correlations between the activation energies of DMDS hydrolysis and temperatures. However, the activation entropy absolute values of DMDS hydrolysis increased with increasing temperatures, suggesting that the hydrolysis of DMDS in aqueous solutions was driven by activation entropy. The hydrolysis rates of DMDS in natural water samples are as follows: rice paddy field water > Grand Canal water > tap water. Sterilization of three kinds of natural water samples showed that biodegradation accounted for 4.08, 21.52, and 8.82% in tap water, paddy field water, and Grand Canal water, respectively. This research result has important implications in the scientific evaluation of DMDS.

Mercury (Hg) is an environmental pollutant which is detrimental to the health of living beings due to the toxicity in its all oxidation states. To control mercury pollution development of low cost, efficient and highly sensitive prototype mercury sensor remains a challenge. In the present work, we have proposed a low-cost prototype device based on silver nanoparticle-impregnated poly(vinyle alcohol) (PVA-Ag-NPs) nanocomposite thin film for mercury detection. The thin film, fabricated through a facile protocol, is shown to be a fast, efficient, and selective sensor for Hg²⁺ in aqueous medium with a detection limit of 10 ppb. We have utilized the aggregation and amalgamation of Ag-NPs with Hg²⁺ to develop the low-cost, highly efficient and feasible prototype mercury sensor. In the presence of Hg²⁺, the yellowish thin film turned into colourless due to the loss of intense surface plasmon resonance (SPR) absorption band of the silver nanoparticles (Ag-NPs) through aggregation and amalgamation with mercury. The developed sensor has high selectivity for Hg²⁺ ions over a wide range of other competing heavy metal ions, generally present in water of natural sources. The sensor response is found to be linear over the Hg²⁺ ion concentration regime from 10 ppb to 5 ppm. The developed sensor has shown to determine a trace Hg²⁺ ions in real water samples. Finally, using the proposed technique, we have developed a simple and inexpensive prototype device for monitoring in field environmental mercury pollution. Graphical Abstract ᅟ

Dissipation rates of copper following algaecide treatments resulting in pulse exposures can be accurately modeled if the component dissipation rates are known. Scaled experiments (in situ, laboratory and mesocosm) were used to parse and rank dominant processes from concurrent processes affecting copper fate in pulse exposures. Copper dissipation rates were measured cumulatively in situ and in mesocosms as well as individually in laboratory experiments. Predictions of the influence of individual dissipation rates on the cumulative dissipation rate were assessed mathematically. In situ aqueous copper dissipated rapidly following an algaecide treatment, with a measured half-life of 0.03 days. Based on laboratory experiments, the most rapid copper fate process was dilution with a half-life of 0.03 days, followed by sediment sorption with a half-life of approximately 3 days. Mesocosm experiments incorporating physical characteristics of the site (i.e., dilution, sediment, algae, and site water) resulted in similar copper dissipation rates (0.02 days) relative to the in situ copper dissipation rate. Prediction of the fate of copper from algaecide treatments requires incorporation of accurate estimates of dominant fate processes that can be determined physically and mathematically.

The objectives of this study were to determine and compare the concentrations of Hg, Cd, Pb, Zn, Cu, Ni and Se in the liver of macrourid fish as Trachyrinchus scabrus, Nezumia sclerorhynchus and Coelorhynchus coelorhynchus from the Mediterranean Sea, Italy. It was also carried out to evaluate the relationship between metal concentration and fish size and to explore selenium/mercury molar ratio. The highest concentrations were in T. scabrus, followed by N. sclerorhynchus and C. coelorhynchus. In all species, any element displayed significant correlation between metal body burden and fish size, except Hg. The mean selenium/mercury ratios were greater than one in all fish species indicating that Se antidotal effect in counteracting Hg occurred. This report represents one of the few surveys providing information on trace metal in deep-sea fish from Mediterranean Sea constituting, thus, an essential baseline work with which future levels may be compared.

The evaluation of DNA damage in aquatic organisms represents one of the most widely used biomarkers in the assessment and monitoring of marine pollution. Our previous research highlighted the presence of DNA damage in hepatic nuclei and blood cells of Coris julis specimens collected from Augusta harbor (Syracuse, Italy), a site highly polluted. In this work, we investigated on the ability of different natural compounds with antioxidant and immunostimulating properties, such as resveratrol (50 μM, 100 μM), amygdalin (100 μM, 200 μM), and Urtica dioica roots extract (50 and/or 100 μg/ml), in reducing DNA damage of C. julis. Blood cells were analyzed by atypical cellular comet assay. The results confirmed that Augusta specimens are the most damaged and showed that resveratrol, followed by amygdalin and U. dioica roots extract, drastically reduced DNA damage. This finding evidences the effectiveness of three natural compounds for DNA protection suggesting the possible use of feed enriched with antioxidant compounds in aquaculture practices for organisms damaged by natural and anthropic insults.

Copper is an active component of some commercial algaecides and is commonly found in low concentrations in contaminated aquatic systems. Unintended consequences of algaecide application include macrophyte bioaccumulation and possible trophic level bioamplification especially by specialist herbivores. Trophic level effects of copper contamination were observed through feeding trials using the mustard beetle (Phaedon viridis). Several metals, including copper, interfere with the myrosinase enzyme system responsible for the watercress (Nasturtium officinale) allelopathic defense against herbivory. The mustard beetle is a specialist herbivore that has evolved a detection system that is stimulated by the products of the glucosinolate-myrosinase system. Because copper interferes with myrosinase enzymes, mustard beetles were expected to avoid copper-contaminated plants. While larvae exhibited a slight preference for contaminated plants, adult mustard beetles in this experiment exhibited a statistically significant preference for plants uncontaminated with copper.

In the present research, the distribution and subcellular localization of cadmium in the roots, shoots, and leaves of Monochoria hastata were evaluated to understand structural and ultrastructural changes caused by the metal. Several visual toxic symptoms such as withering, chlorosis, and falling of leaves appeared in M. hastata, especially at 15 mg L⁻¹ Cd concentration. Analysis of Cd concentration by ICP-OES showed that Cd concentrations in the root were significantly higher than those in the shoot and found to be in the following order: root > stem > leaf. Bioconcentration factor (BCF) and translocation factor (TF) were used to evaluate accumulation and transfer of metals from the root to aerial parts. TF of Cd in M. hastata was <1 in all three Cd concentrations. But it has quite considerable extent of BCF value suggesting that M. hastata is a moderate accumulator. SEM has provided a strong evidence of closing of stomata due to Cd-induced stress. The results of TEM showed the deposition of electron-dense material in vacuoles, cell wall, chloroplasts, and mitochondria. Besides, significant ultrastructural changes such as changes of the shapes of the chloroplasts, reduction of the number of cristae, high vacuolization in the cytoplasm, decrease in the intercellular spaces, shrinkage of vascular bundle, and loss of cell shape were observed in the TEM micrograph study. FTIR analysis revealed the presence of different functional groups which are responsible for binding of Cd ions in the biomass. From the above study, it is clear that M. hastata can potentially be useful for the removal of Cd from Cd-containing wastewater.

In two soils from Central Greece, a pot experiment was conducted with the addition of mixture at various ratios of zeolite and compost (based on Posidonia oceanica (L.) leaves) applied at a rate of 5% w/w (calculated on a soil dry weight basis). Three varieties of tobacco (Burley, Virginia, and Oriental) were cultivated, and Cu, Zn, and Cd concentrations in tobacco leaves were measured at first, second, and third primings. We found that the addition of zeolite in the soil1 led to a significant reduction of metal concentration in all three tobacco varieties compared to the control. Also, zeolite addition reduced significantly the water-soluble, as well as, DTPA-extractable metal concentrations, compared to the other treatments. Our results suggest that the most effective amendment in soil 1 was the mixture consisting of 20% compost and 80% zeolite; this mixture led to higher reduction of metal concentration in all tobacco varieties. As for soil 2, which had almost twice as high Cd concentrations as than in soil 1, Posidonia compost was more effective in reducing Cd concentrations from all three tobacco varieties. In all cases studied, both in soils 1 and 2, Cd concentration was higher in Burley tobacco leaves. The results indicate that a mixture of zeolite and compost consisting of Posidonia oceanica (L.) is a low-cost soil conditioner that is effective in reducing tobacco Cu, Zn, and Cd uptake.

Two species of Pb-adapted shrubs, Alyssum montanum and Daphne jasminea, were evaluated in vitro for their tolerance to elevated concentrations of cadmium. Shoot cultures were treated with 0.5, 2.5, and 5.0 μM CdCl₂ for 16 weeks and analyzed for their organogenic response, biomass accretion, pigment content, and macronutrient status. Cadmium accumulation and its root-to-shoot translocation were also determined. In both species, rooted microplantlets, suitable for acclimatization, were obtained in the presence of Cd applied as selection agent. In A. montanum, low and moderate dose of Cd stimulated multiplication, rooting, and biomass production. Growth tolerance index (GTI) in Cd-treated shoots ranged from 120 to 215%, while in the roots 51–202%. In turn, in Cd-treated D. jasminea proliferation and rooting were inhibited, and GTI for shoots decreased with increasing doses of Cd. However, roots exposed to Cd had higher biomass accretion. Both species accumulated Cd in developed organs, and its content increased with increasing CdCl₂ dose. Interestingly, D. jasminea accumulated higher amounts of Cd in the roots than A. montanum and immobilized this metal in the root system. On the contrary, A. montanum translocated some part of accumulated Cd to the shoots, but with low efficiency. In the presence of Cd, A. montanum maintained macronutrient homeostasis and synthesized higher amounts of phytosynthetic pigments in the shoots. D. jasminea accumulated root biomass, immobilized Cd, and restricted its translocation at the expense of nutrient balance. Considering remediation potential, A. montanum could be exploited in phytoextraction, while D. jasminea in phytostabilization of polluted substrate.

A magnetic chitosan-modified Fe₃O₄@SiO₂ with sodium tripolyphosphate adsorbent (MTPCS) was synthesized by surface modification of Fe₃O₄@SiO₂ with chitosan using sodium tripolyphosphate (STPP) as the cross-linker in buffer solution for the adsorption of Cu(II) ions from aqueous solution. The structure and morphology of this magnetic nanoadsorbent were examined by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), BET surface area measurements, Fourier transform infrared spectrometer (FTIR), and X-ray photoelectron spectroscopy (XPS). The effects of initial pH, adsorbent amount, and initial concentration of heavy metal ions were investigated by batch experiments. Moreover, adsorption isotherms, kinetics, and thermodynamics were studied to understand the mechanism of adsorbing metal ions by synthesized MTPCS. The results revealed that adsorption kinetics was best depicted by the pseudo-second-order rate mode and intraparticle-diffusion models. The adsorption isotherm fitted well to the Langmuir model. Moreover, thermodynamic study verified the adsorption process was endothermic and spontaneous in nature. The maximum adsorption occurred at pH 5 ± 0.1, and the adsorbent could be used as a reusable adsorbent with convenient conditions.