With a mean precipitation rate, much lower than that of the world, Iran is among the countries that face severe water challenges. The present study has dealt with the evaluation of hydrochemistry of Faryab spring water in Hormozgan Province, Iran. Four different composite water samples have been analyzed to detect major anions, cations, total dissolved solids, electrical conductivity, pH, and sodium absorption ratio. The dominant water type was detected as sodium-chloride, with remarkable high concentration of sodium and chloride ions that makes it unfit for drinking purposes. Regarding irrigation use, high values of electrical conductivity (29989 to 31983 µS/cm) and sodium absorption ratio (SAR) (58.1 to 61) indicate a very high risk level for salinity and sodium alkali hazards, respectively. Abundance of secondary minerals such as halite and gypsum is considered to be the main reason for remarkably-high TDS values. Intensity of salt domes within the area would also facilitate solution/dissolution process of Na+ and Cl- into water column.

Population’s exponential growth along with drought has increased water resources limitation, especially in arid and semi-arid area. Therefore, the use of non-conventional water is an important tool for water resource management. If unconventional water has no negative impact on soil properties and water, it can be used for irrigation coupled with desertification projects. So, this paper tries to present the effect of irrigation with municipal wastewater, salt water, brackish water, and combination of salty water and wastewater on some soil properties including nitrogen, phosphorus, and potassium in Qom plain. Soil samples were taken from agricultural land treated by wastewater, saline water, brackish water, combination of salty water, and wastewater and range land as control in five treatments from depths of 0-30 and 60-90 centimeter. The results showed that wastewater has increased the amount of N, P, and K to other treatments and control area. The concentration of potassium in surface layer of area treated by combination of salty water and wastewater with amount of 459.39 ppm has the most significant difference to control and other treatments. Also, the maximum amount of nitrogen was observed in sub layer of saline and brackish water treatment with amount of 0.08 percent.

For the availability of drinking water, saline water treatment has become exceedingly necessary. The purpose of this research was to determine how efficient electrocoagulation (EC) with monopolar iron electrodes was for desalinating water from Iraq’s Sawa Lake. Absolute dissolved solids (TDS), chloride (Cl), bromine (Br), and sulfate (SO4) are some of the salty water forms that are being targeted. The impacts of five considerations on treatment efficiency were studied, including current (I), detention time (RT), pH, speed of mixing stirring (Mrpm), and inter-electrode distance (IED). I=0.8A, RT=80 minutes, pH=8, IED=1cm, and Mrpm=500 were found to be the best values. TDS, Cl, Br and SO4 removal efficiencies were 91 percent, 93 percent, 92 percent, and 90 percent, respectively, under ideal conditions. It can be inferred that the EC system used in this research was operative in removing salts from the water of Sawa lake.

To evaluate the chemical status of groundwater bodies (GWB) according to the European Groundwater Directive, EU Member States are required to take into account natural background levels (NBLs) where needed. Assessing the NBLs in coastal GWBs is complicated by seawater intrusion which can be amplified by groundwater withdrawals increasing the salinization of such groundwater systems. This paper proposes a new method for the NBLs assessment in coastal areas based on a double pre-selection (PS) with fixed/dynamic limits. A case study in the Apulia region, located in southeastern Italy, is proposed, where we investigated four adjacent GWBs which form the complex karst, fractured Murgia aquifer, hosted in the Jurassic-Cretaceous carbonate platform, bounded by two seas and sustained by saltwater of marine intrusion in the coastal areas. Data related to 139 monitoring stations (MSs) of the regional groundwater monitoring network were used. The first PS, “static”, based on a fixed limit of anthropogenic contamination markers (NO₃ and NH₄), allows for the elimination of MSs impacted by human activities. On these, the second PS, “dynamic”, based on the identification of Cl anomalous values, allows for the identification of additional MSs affected by saline contamination. The residual dataset of MSs was used for the definition of NBLs of Cl, SO₄, F and B. A statistical comparison with historical Cl observations finally allowed us to verify if the salinity of current groundwater is representative of pristine conditions. The calculated NBLs of salinity parameters are higher for the two coastal GWBs, with chloride values between 0.8 and 2 mg/L. Conversely, fluorides always show very low NBLs. The double PS approach seems more effective for NBLs calculation in coastal aquifers affected by saline contamination, where the use of a fixed Cl limit fails. It may respond to the international needs for a standardized procedure for NBL assessment.

Many estuaries have undergone severe saltwater intrusion in addition to simultaneously experiencing serious heavy metal pollution. To explore the effect of water density stratification associated with saltwater intrusion on the behaviour of heavy metals (Cr, Co, Ni, Cu, Zn, As, Pb, and Cd) in water and sediments, a field survey was conducted in a typical estuary (Modaomen). The content, distribution, and mobility of heavy metals were investigated, as well as the influence of environmental factors on their future. The results showed that Modaomen estuary was characterised by a notable variation in salinity along the estuary, presenting total freshwater upstream, high salinity stratification water in the mouth, and saltwater offshore. Dissolved metals presented a prominent gradient vertically, with 1.2–2.1 times higher in bottom water than in surface water and the highest contents in the highly–stratified bottom water. Elevated salinity and restricted mixing induced by water stratification were likely the causes of this outcome. The distribution of heavy metals in sediments was greatly governed by grain size, Fe/Mn (hydr)oxides, total organic carbon, salinity, and dissolved oxygen. Comprehensive evaluation, combined with total contents and chemical fractions of heavy metals, indicated that internal release from sediments contributed a considerable part to the higher levels of heavy metals in bottom water, particularly for Zn and Pb, which was fully consistent with their status in water body, and elevated salinity and lack of oxygen were likely the primary driving factors. During the phase-partition processes between bottom water and sediments, partitioning coefficients were markedly lower in the highly stratified zone, implying that saltwater intrusion facilitated the mobility and repartitioning processes of metals. Because of increased levels and toxicity of heavy metals in water and extended residence time during saltwater intrusion, the potential damage to the estuarine ecosystem should receive more attention.

The Pearl River Estuary (PRE), the largest estuary in Southern China, historically has suffered from metal contamination as a result of inputs from different riverine discharges. Determining the sources of metals accumulation in local aquatic flora and fauna remains a great challenge for this estuarine system with complex water circulation. In this study, Zn isotope ratios were measured in local oysters (Crassostrea hongkongensis) collected at 8 locations in the estuary on four occasions from 2014 to 2018, to better understand and assess the contamination sources. The results showed no significant differences (p < 0.05) in δ⁶⁶Zn values in oysters among the four sampling dates within individual sites. However, approximately a 0.67‰ (range from -0.66‰ to 0.01‰) difference in average δ⁶⁶Zn values was consistently found in oysters collected from the east side of the estuary compared to the west side, despite their comparable Zn concentrations. A mixing model was subsequently used to estimate the relative contributions from various sources to the δ⁶⁶Zn values in these oysters. The mixing model predicts that zinc derived from the dissolved fraction (approximately 80 %) was the dominant uptake pathway for oysters collected at the east shore whereas approximately 50 % of the Zn in oysters collected at the west shore was derived from the particulate fraction. The mixing model also was used to estimate the relative impacts of fresh versus saline water on the measured δ⁶⁶Zn values. Contributions from these two sources also varied between the east and west shores. This study presents the first data for Zn isotope ratios in oysters from the PRE, providing new insight for using Zn isotope ratios in oysters as a powerful tracer of sources in a complex estuarine system.

In this study, a novel rotating anode-based reactor (RAR) was designed to investigate its effectiveness in removing dissolved salts (i.e., Br⁻, Cl⁻, TDS, and SO₄²⁻) from saline water samples. Two configurations of an impeller’s rotating anode with various operation factors, such as operating time (min), rotating speed (rpm), current density (mA/cm²), temperature (°C), pH, and inter-electrode space (cm), were used in the desalination process. The total cost consumed was calculated on the basis of the energy consumption and aluminum (Al) used in the desalination. In this respect, operating costs were calculated using optimal operating conditions. Salinity was removed electrochemically from saline water through electrocoagulation (EC). Results showed that the optimal adjustments for treating saline water were carried out at the following conditions: 150 and 75 rpm rotating speeds for the impeller’s rod anode and plate anode designs, respectively; 2 mA/cm² current density (I), 1 cm² inter-electrode space, 25 °C temperature, 10 min operation time, and pH 8. The results indicated that EC technology with impeller plates of rotating anode can be considered a very cost-effective technique for treating saline water.

Elevated inorganic arsenic concentrations in groundwater has become a major public and environmental health concern in different parts of the world. Currently, As-contaminated groundwater issue in many countries and regions is a major topic for publications at global level. However, there are many regions worldwide where the problem has still not been resolved or fully understood due to inadequate hydrogeochemical investigations. Hence, this study evaluates for the first time the hydrogeochemical behavior of the arid and previously unexplored inland basin of Sirjan Plain, south east (SE) Iran, in order to assess the controlling factors which influence arsenic (As) mobility and its distribution through groundwater resources. Total inorganic arsenic concentration was measured using inductive-coupled plasma optical emission spectrometry (ICP-OES). Arsenic content in groundwater of this region ranged between 2.4 and 545.8 μg/L (mean value: 86.6 μg/L) and 50% of the samples exceeded the World Health Organization (WHO) guideline value of 10 μg/L in drinking water. Groundwater was mainly of Na-Cl type and alkaline due to silicate weathering, ion exchange and evaporation in arid conditions. Elevated As concentrations were generally observed under weakly alkaline to alkaline conditions (pH > 7.4). Multivariate statistical analysis including cluster analysis and bi-plot grouped As with pH and HCO3 and demonstrated that the secondary minerals including oxyhydroxides of Fe are the main source of As in groundwater in this region. The desorption of As from these mineral phases occurs under alkaline conditions in oxidizing arid environments thereby leading to high levels of As in groundwater. Moreover, evaporation, ion exchange and saltwater intrusion were the secondary processes accelerating As release and its mobility in groundwater. Based on the results of this study, desorption of As from metal oxy-hydroxides surfaces under alkaline conditions, evaporation and intrusion of As-rich saline water are considered to be the major factors causing As enrichment in arid inland basins such as those in southeast Iran. This study proposes the regular monitoring and proper groundwater management practices to mitigate high levels of arsenic in groundwater and related drinking water wells of Sirjan Plain.

Use of titanium dioxide nanoparticles (TiO2 NPs) has become a part of our daily life and the high environmental concentrations predicted to accumulate in aquatic ecosystems are cause for concern. Although TiO2 has only limited reactivity, at the nanoscale level its physico-chemical properties and toxicity are different compared with bulk material. Phytoplankton is a key trophic level in fresh and marine ecosystems, and the toxicity provoked by these nanoparticles can affect the structure and functioning of ecosystems. Two microalgae species, one freshwater (Chlamydomonas reinhardtii) and the other marine (Phaeodactylum tricornutum), have been selected for testing the toxicity of TiO2 in NP and conventional bulk form and, given its photo-catalytic properties, the effect of UV-A was also checked. Growth inhibition, quantum yield reduction, increase of intracellular ROS production, membrane cell damage and production of exo-polymeric substances (EPS) were selected as variables to measure.TiO2 NPs and bulk TiO2 show a relationship between the size of agglomerates and time in freshwater and saltwater, but not in ultrapure water. Under two treatments, UV-A (6 h per day) and no UV-A exposure, NPs triggered stronger cytotoxic responses than bulk material. TiO2 NPs were also associated with greater production of reactive oxygen species and damage to membrane. However, microalgae exposed to TiO2 NPs and bulk TiO2 under UV-A were found to be more sensitive than in the visible light condition. The marine species (P. tricornutum) was more sensitive than the freshwater species, and higher Ti internalization was measured. Exopolymeric substances (EPS) were released from microalgae in the culture media, in the presence of TiO2 in both forms. This may be a possible defense mechanism by these cells, which would enhance processes of homoagglomeration and settling, and thus reduce bioavailability.

Corrosion is an environmental and economic global problem. “Smart” or stimuli-responsive colorimetric nanosensors for maritime coatings have been proposed as an asset to overcome the limitations of the current monitoring techniques by changing color in the presence of triggers associated with the early stages of corrosion. Layered double hydroxides (Zn–Al LDH; Mg–Al LDH) and silica mesoporous nanocapsules (SiNC) were used as precursor nanocarriers of active compounds: hexacyanoferrate ions ([Fe(CN)₆]³⁻) and phenolphthalein (PhPh), respectively. Additionally, the safer-by-design principles were employed to optimize the nanosensors in an eco-friendly perspective (e.g., regular vs. warm-washed SiNC-PhPh; immobilization using different carriers: Zn–Al LDH-[Fe(CN)₆]³⁻ vs. Mg–Al LDH-[Fe(CN)₆]³⁻). Therefore, the present study aims to assess the environmental behavior in saltwater and the toxic effects of the nanosensors, their nanocarriers, and the active compounds on the marine microalgae Tetraselmis chuii and the crustacean Artemia salina. Briefly, tested compounds exhibited no acute toxic effects towards A. salina (NOEC = 100 mg/L), apart from SiNC-PhPh (LC₅₀ = 2.96 mg/L) while tested active compounds and nanosensors caused significant growth inhibition on T. chuii (lowest IC₅₀ = 0.40 mg/L for SiNC-PhPh). The effects of [Fe(CN)₆]³⁻ were similar regardless of the nanocarrier choice. Regarding SiNC-PhPh, its toxicity can be decreased at least twice by simply reinforcing the nanocapsules washing, which contributes to the removal (at least partially) of the surfactants residues. Thus, implementing safe-by-design strategies in the early stages of research proved to be critical, although further progress is still needed towards the development of truly eco-friendly nanosensors.