Acute toxicity of chlorpyrifos (CP) and its principal metabolite 3,5,6-trichloro-2-pyridinol (TCP) alone and in combination have been evaluated using a test battery comprising aquatic organisms from different trophic levels: luminescent marine bacteria Aliivibrio fischeri, freshwater unicellular alga Pseudokirchneriella subcapitata, and cladoceran Daphnia magna. As expected, D. magna was the more sensitive organism to the compounds tested, being CP more toxic than its metabolite. On the contrary, TCP was found to be more toxic than its parental compound to A. fischeri and P. subcapitata. In all cases, the mixture of CP and its metabolite was more toxic than the compounds tested separately, multiplying between 5 and 200 times CP toxicity level and up to 15 times TCP toxicity level. These results indicate that the co-existence of parent chemical and its degradation product in the environment can result in a synergic interaction involving high risk to the aquatic ecosystems. Graphical abstract

Many organic dye pollutants have been identified in rivers and lakes around the world, and concern is growing with them as they cause serious changes in the ecological balance of aquatic environments. One of these dyes is rhodamine R6G, which is very water-soluble and has a high corrosive power. Therefore, Clitoria fairchildiana (CF) pods were used as a biosorbent to remove R6G from synthetic dye effluents. CF was characterized by infrared spectroscopy, thermogravimetric analysis, x-ray diffraction, elemental analysis, Boehm titration, and zero charge point measurements. The influence of various factors, such as solution pH, contact time, adsorbent mass, and concentration of R6G, was studied using batch equilibrium experiments. The optimum contact time to reach equilibrium was found to be 15 min, while the optimum adsorbent dose was 8 g L⁻¹. The maximum adsorption capacity of CF (73.84 mg g⁻¹) was observed at pH 6.4 and 298.15 K. Adsorption kinetics followed a pseudo-second-order law, and the isotherm could be best fitted with a Liu model. The obtained thermodynamic parameters indicate that the adsorption of R6G is spontaneous and enthalpy-driven. We thus conclude that CF is an efficient, green, and readily available biosorbent for dye removal from wastewater.

During the past decade, nanotechnologies opened a new era in delivery of plant protection products through the development of nanosized controlled release systems, such as polymer nanoparticles, micelles, and so on using a wide variety of materials. To increase the pesticides penetration into the grain under the presowing seed treatment, a new approach based on non-covalent associate preparation with natural polysaccharides and oligosaccharides as delivery systems (DSs) was applied. Earlier, this approach was tested on antidote 1,8-naphthalic anhydride (NA). Enhancement of the NA solubility and penetration into the barley and wheat seeds had been demonstrated. In the present study, these DSs were used to prepare nanocomposites of pesticides (tebuconazole, imidacloprid, imazalil, prochloraz). The composite formation of the pesticides with poly- and oligosaccharides was proved by NMR relaxation method. Enhancement of the pesticides solubility and improvement of its penetration into the seeds of corn and rapeseeds has been detected. The strongest enhancement of penetration ability was observed for arabinogalactan nanocomposites: 5-folds for tebuconazole and imidacloprid, and more than 10-folds for imazalil and prochloraz. Our data show that the effect of polysaccharides and oligosaccharides on the nanopesticide penetration might be associated with the solubility enhancement, affinity of DSs to the surface of grains, and the modification of cell membranes by poly- and oligosaccharides.

The majority of dosimeters currently in use are synthetic and very expensive. Therefore, the study of the dosimetric characteristics of polyphenolic extracts of xerophytes is useful because drought stress causes an increase in the production of these cheap and natural compounds containing benzene rings. Here, the polyphenolic compounds were extracted from Rhamnus lycioides which was collected from Bou-Hedma National Park in Tunisia and identified using liquid chromatography-mass spectrometry (LC-MS). We investigated the impact of cobalt-60 (⁶⁰Co) irradiation (0–30 kilogray (kGy)) on the color parameters of polyphenolic extracts of R. lycioides using the Konica Minolta CR 300 portable colorimeter and UV–Visible spectroscopy. The structural and morphological characteristics of the irradiated extracts were assessed using Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) technique and scanning electron microscopy (SEM). Overall, our results suggest that exposure to ionizing radiation (IR) of the polyphenolic components of the xerophyte R. lycioides has produced significant dose-dependent changes in their optical and morphological properties. Thus, these extracts can be valorized as biodosimeters in the dose range from 5 to 25 kGy.

The ranking of power generation sources is a very important prerequisite for power generation installation planning and power supply security. This study proposed a new multi-criteria system for ranking regional power generation sources in one country, including resources, economy, technology, environment, and society, using 11 sub-criteria. Based on the system, a novel decision-maker (DMs) preference-based integrated MCDM framework involving four methods (Visekriterijumsko Kompromisno Rangiranje (VIKOR), Technique for Order Preference by Similarity to Ideal Solution (TOPSIS), Preference Ranking Organization Method for Enrichment Evaluations (PROMETHEE), and Weighted Sum Method (WSM)) was developed for ranking six power generation sources (thermal, nuclear, wind, hydro, solar PV, and biomass) at the level of China’s 30 provinces. Six different preferences of DMs are considered in the ranking according to five criteria. The results show that wind should be the power generation source given the top priority in most provinces in China whereas nuclear power and thermal power are the last choice for 26 provinces. Biomass is the most preferable power source for 17 provinces based on technological preference in which DMs regard the technology criteria is prior to all other criteria. Thermal power would still the preferred or secondary power source for provinces rich in coal resources such as Shanxi, Inner Mongolia, Henan, and Shaanxi.

Zinc oxide nanoparticles are widely used in some domains (cosmetics, pharmaceuticals optical devices, and agricultural field) due to their physical, optical, and antimicrobial properties. However, the release of ZnO-NPs into the environment may affect organisms like fish with potential consequences for human health. Histological approaches of the acute effects of these materials on fish are scarce; thus, the present study aimed to investigate the potential toxic effects of acute exposure to ZnO particles in marine environments, by assessing histological changes in the gills, liver, spleen, and muscle of gilthead seabream (Sparus aurata) juveniles. Thus, fish were exposed for 96 h, via water, to 1 mg L⁻¹ of ionic zinc and zinc oxide particles (1.1, 1.2, and 1.4 μm of size). Histological examination revealed gills as the most affected organ, followed by liver, muscle, and spleen. In the gills, histopathological changes included hyperplasia of epithelial cells, fusion of the secondary lamellae, and lifting of the lamellar epithelium with edema. In the liver, lipid vacuolation of several degrees, necrosis of hepatic and pancreatic tissues, blood congestion in sinusoids and hepatoportal vessels, presence of cellular infiltrate, and melano-macrophages diffusion was found. Muscle showed degeneration, atrophy, thickening and necrosis of muscle fibers with edema between them, and presence of melano-macrophages in the muscle layer. Spleen was the less damaged organ, displaying congested blood, white pulp increase/rupture, and bigger and darker melano-macrophage aggregates in the splenic stroma. These results underline that the size of particles plays a determinant role in their potential pernicious effects. A short-term exposure caused major histopathological changes in relevant organs of S. aurata juveniles, possibly affecting their function.

This study focuses on utilizing a plant-derived urease enzyme (PDUE)–urea mixture to remove heavy metals from water as constituents of nano-carbonate minerals. The bio-removal process was conducted by individually mixing PbCl₂, CuCl₂, and NiCl₂ solutions with a PDUE–urea mixture, followed by incubation for 24 h at 23 ± 2 °C. The preliminary results revealed that the proposed method exhibited high Pb removal efficiency (˃ 99%) in a short time (8 h); meanwhile, moderate Cu and Ni removal efficiencies (67.91% and 58.49%, respectively) were obtained at the same incubation time. The concentration of heavy metals (50–200 mM) had an insignificant effect on the bio-removal rate, indicating that the PDUE–urea mixture is highly effective for the removal of heavy metals at different concentrations. The bio-removal process involved the transformation of soluble heavy metals into insoluble carbonate materials. A spherically shaped nano-cerussite (4–15 nm), a malachite hexahydrate nanosheet (thickness 8 nm), and an ultrafine micro-hellyerite (thickness 0.3 μm) were the main minerals produced by the Pb, Cu, and Ni bio-removal processes, respectively. As a beneficial application, nano-cerussite was used as an additive in an alkali-activated slag/ceramic waste-based geopolymeric coating. A preliminary study proved that increasing the nano-cerussite content enhanced the resistance of the geopolymeric coating to sulfur-oxidizing bacteria, which is detrimental to normal concrete, particularly in sewer systems.

A rare super-large fractured karst aquifer located in Zibo city, Shandong Province of Northern China was polluted by petroleum hydrocarbons from a petrochemical company. Over the last 30 years, it has been the focus of several remediation efforts. In this study, the contamination and natural attenuation characteristics of the petroleum hydrocarbons were elucidated using hydrogeochemical indicators (DO, DOC, Cl⁻, HCO₃⁻, pH, NO₃⁻, and SO₄²⁻), petroleum hydrocarbons elements and environmental isotopes (δ¹⁵NNO₃, δ¹⁸ONO₃, δ¹³CDIC, and δ¹³CDOC). With the aid of GIS, statistical analyses, as well as first-order decay model and electron-acceptor-limited kinetic model, the spatio-temporal evolution characteristics of the petroleum hydrocarbons were modeled. Results showed a positive natural attenuation trend over the last 3 decades where intrinsic biodegradation mechanism was found to be the most important factor driving the degradation of hydrocarbons in the aquifer system. The hydrogeochemical association between the indicators and petroleum hydrocarbons provided the evidences of biodegradation and also served as markers, highlighting the occurrence of anaerobic respiration without methanogenic activities within the heterogenous karst media. Furthermore, the mean natural attenuation rate of petroleum hydrocarbons was calculated to be 3.76 × 10⁻³/day whereby the current highest petroleum hydrocarbons concentration (361.13 μg/L) is estimated to be degraded completely in 6 years under the present hydrogeological and environmental conditions.

A combined approach based on multiple X-ray analytical techniques and conventional methods was adopted to investigate the distribution and speciation of Cr in a polluted agricultural soil, from the bulk-scale down to the (sub)micro-level. Soil samples were collected from two different points, together with a control sample taken from a nearby unpolluted site. The bulk characterization revealed that the polluted soils contained much higher concentrations of organic matter (OM) and potentially toxic elements (PTE) than the control. Chromium was the most abundant PTE (up to 5160 g kg⁻¹), and was present only as Cr(III), as its oxidation to Cr(VI) was hindered by the high OM content. According to sequential extractions, Cr was mainly associated to the soil oxidisable fraction (74%) and to the residual fraction (25%). The amount of Cr potentially bioavailable for plant uptake (DTPA-extractable) was negligible. Characterization of soil thin sections by micro X-ray fluorescence (μXRF) and field emission scanning electron microscopy coupled with microanalysis (FEGSEM-EDX) showed that Cr was mainly distributed in aggregates ranging from tens micrometres to few millimetres in size. These aggregates were coated with an aluminosilicate layer and contained, in the inner part, Cr, Ca, Zn, P, S and Fe. Hyperspectral elaboration of μXRF data revealed that polluted soils were characterised by an exogenous organic-rich fraction containing Cr (not present in the control), and an endogenous aluminosilicate fraction (present also in the control), coating the Cr-containing aggregates. Analyses by high-resolution micro X-ray computed tomography (μCT) revealed a different morphology of the soil aggregates in polluted soils compared with the control. The finding of microscopic leather residues, combined with the results of bulk- and micro-characterizations, suggested that Cr pollution was likely ascribable to soil amendment with tannery waste-derived matrices. However, over the years, a natural process of Cr stabilization occurred in the soil thus reducing the environmental risks.

This study aims to investigate the distribution of heavy metals (Cd, Pb, Ni, and Mn) in different organs of two marine mussel species, Perna perna collected from Figuier site and Mytilus galloprovincialis sampled from Sercouf and Algiers port sites of the Algerian coast. Thirty individuals (>5 cm length) were seasonally sampled over a 1-year period from each site, and condition index (CI) and gonado somatic index (GSI) of mussels were calculated. The gill, digestive gland, rest of soft tissues, and gonad were accurately isolated and heavy metal contents were analyzed by ICP-MS. Heavy metal results, expressed on μg/g dry weight, ranged from 0.1 to 2.6 Cd, 0.1 to 17.15 Pb, 0.36 to 25.7 Ni, and 3.68 to 74.76 Mn. Thus, typical distribution of studied metals in various organs of mussels was found. In fact, the digestive gland followed by gill revealed significantly high metal concentrations. However, gonad showed low heavy metal contents. Different patterns of heavy metal distribution in various organs of mussels were found at the three sampling sites. High levels of Cd, Pb, Ni, and Mn were detected in mussels of Sercouf, Algiers port, and Figuier sites, respectively. According to the Algerian and European norms, mussels collected from all sites were healthy except those of Algiers port sampled in autumn and winter seasons where lead contamination was found.