The present study aimed to survey the spatial and temporal trends of ambient concentration of PM₂.₅ and to estimate mortality attributed to short- and long-term exposure to PM₂.₅ in Isfahan from March 2014 to March 2019 using the AirQ⁺ software. The hourly concentrations of PM₂.₅ were obtained from the Isfahan Department of Environment and Isfahan Air Quality Monitoring Center. Then, the 24-h mean concentration of PM₂.₅ for each station was calculated using the Excel software. According to the results, the annual mean concentration of PM₂.₅ in 2014–2019 was 29.9–50.9 μg/m³, approximately 3–5 times higher than the WHO guideline (10 μg/m³). The data showed that people of Isfahan in almost 58% to 96% of the days of a year were exposed to PM₂.₅ higher than the WHO daily guideline. The concentrations of PM₂.₅ in cold months such as October, November, December and January were higher than those in the other months. The zoning of the annual concentrations of PM₂.₅ in urban areas showed that the highest PM₂.₅ concentrations were related to the northern, northwestern, southern and central areas of the city. On average, from 2014 to 2019, the number of deaths due to natural mortality, lung cancer (LC), chronic obstructive pulmonary disease (COPD), ischemic heart disease (IHD) and stroke associated with ambient PM₂.₅ were 948, 16, 18, 281 and 60, respectively. The present study estimated that on average, 14.29% of the total mortality, 17.2% of lung cancer (LC), 15.54% of chronic obstructive pulmonary disease (COPD), 17.12% of ischemic heart disease (IHD) and 14.94% of stroke mortalities were related to long-term exposure to ambient PM₂.₅. So provincial managers and politicians must adopt appropriate strategies to control air pollution and reduce the attributable health effects and economic losses.

The role of chemical elements in an organism is versatile and multifunctional. However, you should pay attention to the reaction of the organism on the introduction of chemical elements with different biological roles, which is predetermined by the physiological role of organs and body systems. These include the red bone marrow, which primarily responds to endogenous and exogenous factors by its functional significance. Analyzing the myelogram of birds after the various ways of copper NP introduction into the body and the different dosages, we found that, by the end of the experiment, the total numbers of bone marrow cells in all groups were lower than the initial values: in the second group—12.54% lower (p < 0.05), in third—26.32% lower (p < 0.001), for the fourth—14.75% lower (p < 0.05), with exception for the first experimental group where this index was 45.51% higher (р < 0.001). We revealed the following changes in the peripheral blood: the hemoglobin content by the end of the experiment was significantly higher than the initial values: by 18.63% for the first group (p < 0.01); 28.61% higher in the third group (p < 0.001); and 15.76% higher for the fourth (p < 0.01), except the animals of the second group (3.23% lower). The concentration of erythrocytes in all groups was higher than that of the background: by 24.56% (p < 0.001), by 3.37%, by 26.18% (p < 0.001), and by 14.85% (p < 0.01), respectively; the leukocyte concentration in the first group was 39.63% higher (p < 0.001), it remained at the level of the initial values in the other groups. The erythrocyte sedimentation rate in all groups increased by 2.4, 4.0, 2.01, and 1.86 times (p < 0.001), respectively. We revealed that the introduction of copper into an organism in the form of nanopowder both with feed and intramuscularly significantly caused an increase of the content of such elements as arsenic, copper, and silicon and a decrease of calcium, potassium, magnesium, phosphorus, boron, cobalt, iodine, lithium, sodium, zinc, tin, and strontium in the marrowy aspirate. Moreover, compared with the first group (p < 0.01), increasing doses of nanopowders caused a significant rise in the arsenic and tin concentrations and a decline of iodine and strontium. We found that copper nanoparticles ambiguously affect the bone marrow hemopoiesis of poultry; increasing the dose and changing the type of introduction activating the bone marrow hematopoietic function, in particular, granulocyto-, megakaryocyto-, and erythropoiesis.

Efficient analytical methods are required for optimizing dosage of veterinary antibiotics and hormones in order to reduce toxicity and antimicrobial resistance in the environment. Thus, the objective of this work was to develop a rapid and low-cost method for determination of hormone estradiol and antibiotic chlortetracycline in bovine and porcine blood serum by aqueous two-phase system (ATPS) extraction and capillary electrophoresis quantification. ATPS based on ionic liquid cholinium alaninate and citrate salt along with mixtures of protic and aprotic polar solvents were evaluated in terms of recovery of extraction (%R). The liquid-liquid equilibrium, phase diagrams, and tie lines are discussed. Antibiotic migrated to solvent-rich phase (R ≈ 89.0%) to all systems. Estradiol migrates to ionic liquid-rich phase; however, addition of 10% methanol changed partition to solvent-rich phase (R ≈ 89.7%). The method has high recovery and cleanliness, is cost-efficient, scalable, and hence is adequate for screening of antibiotics and hormones tested in animal blood serum for dosage optimization and to predict their environment.

For several decades air pollution has been recognized to hit drastically the skin of human body. Air pollutants predominantly accountable for aging, oxidative damage, and inflammatory allergic reactions led to psoriasis, dermatitis, acne, and skin cancer owing to the impaired functions of DNA, proteins, and lipid biomolecules. Elevated air pollution and its detrimental effects along with variations in physiological parameters of the skin are verily the scaffold for anti-pollution assertions and could be recognized as markers. The present article encompasses the salient features of air pollution and UV radiations besides dreadful effects on human skin physiological parameters and some anti-pollution approaches.

The water-sediment interface of lakes is an important and unique area of the water environment; the geochemical behavior of nutrients in this area has a significant impact on the quality of the water environment and ecosystems, especially in shallow lakes. However, most studies do not provide direct in situ evidence for this in shallow lakes in arid regions; in order to explore the coupling relationship between phosphorus (P) and iron (Fe) in a sediment profile, we conducted a high-resolution analysis of liable Fe and P in sediments taken from the Chaiwopu Lake using ZrO-Chelex thin film diffusion gradient technology (ZrO-Chelex DGT). The results show that (1) the vertical spatial distribution trend of the liable P and Fe in the sediments from each sampling site is essentially similar. The contents of the liable P and Fe ranged from 0.004–0.125 mg/L and 0.050–0.190 mg/L, respectively, and the synchronous distribution of the micro-interface concentration reflects the coupling relationship between them. (2) The correlation analysis of the liable P and Fe concentrations showed that there were significant linear correlations between them (P < 0.05, bilateral). (3) The diffusion fluxes of P and Fe were − 51.76~65.12 μg (m² d)⁻¹ and − 451.27~457.06 μg (m² d)⁻¹, respectively, and were shown to be negative at the sediment-water interface for most of the samples, which showed that P and Fe were released from the overlying water into the sediments. (4) This research showed that the diffusive fluxes at the different sites are quite different, which indicates that the phosphorus and iron pollution in the sediments of the Chaiwopu Lake is affected by exogenous inputs. There was no significant correlation between P release flux and pH, ORP, conductivity (EC), the TDS of the overlying water, or the pH, salinity (Ca²⁺, Mg²⁺), and nutrient (organic matter) content of the sediment. The release flux of Fe is affected by the pH of the sediment. The results of this study provide references for the research of elements in the water-sediment interface of shallow lakes in arid regions, as well as other areas.

A novel adsorbent derived from banyan aerial roots was prepared via modification and employed to aqueous gentian violet (GV) and rhodamine B (RhB) removal. The surface morphology and physicochemical properties of modified banyan aerial roots (MBARs) were investigated by SEM, EDS, N₂ adsorption/desorption, zeta potential, XRD, and FT-IR characterization experiments. Adsorption factors were tested, and the optimal conditions for GV and RhB removal were pH of 6 and 3, doses of 0.02 g and 0.03 g, and reaction time of 540 min. Adsorption isotherm simulation illustrated that theoretical monolayer adsorption capacities of GV and RhB were 456.64 mg/g and 115.23 mg/g, respectively. Kinetics data was assessed with pseudo-first-order and pseudo-second-order models, and the latter described GV and RhB adsorption better at 288 K, 298 K, 308 K, and 318 K. Thermodynamic analysis indicated that GV and RhB adsorption processes were endothermic and spontaneous. From the research results, it could be inferred that GV adsorption was mainly dominated by electrostatic interaction, while RhB adsorption might be primarily attributed to electrostatic interaction and hydrogen bonding. The study based on full utilization of waste plant fibers facilitates recycling of biomass resources, and due to simplicity, safety, and eco-friendliness of the preparation, as well as low cost and high efficiency of the application, MBARs may be potential absorbents for the treatment of dyestuff wastewater.

Humic acid (HA) and water play an important role in polycyclic aromatic hydrocarbons (PAHs) adsorption and biodegradation in soil. In this work, molecular dynamics (MD) and electrostatic potential surfaces (EPSs) simulations are conducted to research the contribution of quartz surface, leonardite humic acid (LHA), and water to PAH adsorption. The adsorption energies between PAHs and LHA are much higher than that between PAHs and quartz. Simulation shows that the hydroxyl and carboxyl groups’ attraction by LHA is the main adsorption force between PAHs and LHA. The π-π interaction between PAHs and LHA also contributes to the adsorption process. In addition, the mobility of water on quartz surface is much higher than that of LHA. Water should be regarded as an adsorbate in the system as well as PAHs. However, the presence of water has a remarkable negative effect on the adsorption of PAHs on LHA and quartz. The bridging effect of water could only enhance the stability of the aggregation system. The adsorption contribution of quartz and LHA to PAHs in the soil model tends to 0 if the water layer reaches 2.0 nm. Graphical abstract

Natural water sources are habitually marred by insidious anthropogenic practices and municipal wastewater discharges that contain either of xenobiotic pollutants and their sometimes more toxic degradation products, or both. Although wastewater is considered as both a resource and a problem, as explained in this review, it is however daunting that, while the global village is still struggling to decipher the mode of proper handling, subsequent discharge and regulation of already established aromatic contaminants in wastewater, there emanates some more aggressive, stealth and sinister groups of compounds. It is quite ironic that majority of these compounds are the ‘go through’ consumables in our present society and have been suspected to pose several health risks to the aquatic ecosystem, eliciting unfavourable clinical manifestations in aquatic animals and humans, which has heightened the uncertainties conferred on freshwater use and consumption of some aquatic foods. This review therefore serves to give a brief account on the metamorphosis of approach in detection of aromatic pollutants and ultimately their implications along the trophic chains in the community.

Anthropogenic activities are a major source for contaminating the agricultural soil with heavy metals, which can affect physiological and metabolic processes in plants. Among the heavy metals, chromium (Cr) is the most toxic pollutant that negatively affects plants’ metabolic activities, growth, and yield. Chromium reduces the plant growth and development by influencing the photosynthetic performance and antioxidant enzyme activities. This study was designed to examine the promotive role of exogenously applied glycinebetaine (GB) on plant morphophysiological and biochemical attributes in cauliflower (Brassica oleracea botrytis L.) under Cr toxicity. Four levels (0, 10, 100, and 200 μM) of Cr were tested under the application of GB (1 mM). The results delineated that Cr stress caused a considerable reduction in plant growth, photosynthetic pigment, gas exchange parameters, and biomass production. At high concentration (200 μM), chromium stress decreased the plant height (57%), root length (32%), number of leaves (45%), and leaf area (29%) as compared with controls. Due to Cr stress, the electrolyte leakage and accumulation of malondialdehyde and hydrogen peroxide increased both in the roots and leaves of cauliflower, whereas antioxidative enzyme activities (SOD, CAT, and POD) decreased both in the roots and leaves of cauliflower due to Cr stress. At 200 μM of chromium treatment, root dry weight, stem dry weight, leaf dry weight, and flower dry weight declined up to 43%, 40%, 53%, and 72%, respectively. With the application of GB, dry biomass of plant increased significantly as compared with no GB treatment under chromium stress. As Cr level increased in growth media, its concentration also increased in all plant parts including roots, stem, leaves, and flowers. However, GB application efficiently alleviated the Cr toxic effects on cauliflower and maintained higher plant growth, biomass production, photosynthetic attributes, and gas exchange traits as compared with their respective controls. Exogenously applied GB decreased oxidative stress and improved antioxidative enzyme activities as compared with treatments without GB application. Furthermore, Cr concentrations taken by plants were decreased due to GB application. These findings suggest that GB can play a positive role to maintain plant morphology and photosynthetic attributes under Cr toxic conditions in cauliflower.

Transport of environmental pollutants in groundwater systems can be greatly influenced by colloids. In this study, the cotransport of Pb²⁺ and silica (SiO₂) colloids at different Pb²⁺ concentrations was systematically investigated by batch adsorption and saturated sand column experiments. Results showed that SiO₂ colloids had low adsorption capacity for Pb²⁺ (less than 1% of the input) compared with sands. In saturated porous media, SiO₂ colloids showed a high mobility; however, with the increase of Pb²⁺ concentration in the sand column, the mobility of SiO₂ colloids gradually decreased. Notably, SiO₂ colloids could facilitate Pb²⁺ transport, although they did not serve as effective carriers of Pb²⁺. Under the condition of low Pb²⁺ concentration, SiO₂ colloids promoted the Pb²⁺ transport mainly through the way of “transport channel,” while changing the porosity of the medium and masking medium adsorption sites were the main mechanisms of SiO₂ colloid–facilitated Pb²⁺ transport under the condition of high Pb²⁺ concentration. The discovery of this non-adsorption effect of colloids would improve our understanding of colloid-facilitated Pb²⁺ transport in saturated porous media, which provided new insights into the role of colloids, especially colloids with weak Pb²⁺ adsorption capacity, in Pb²⁺ occurrence and transport in soil-groundwater systems.