Lighvan hot spring and Toptapan mineral spring are located in the Eastern Azarbaijan, NW of Iran. The host rocks of Lighvan hot spring are dacite, andesite and Quaternary volcanic tuffs. Their main rock forming minerals are quartz, plagioclase, biotite and rarely amphibole. The host rocks of Toptapan mineral water spring are Cretaceous and Jurassic sandstone, shales and carbonate sedimentary rocks. Their main rock forming minerals are quartz, calcite, dolomite and clays. Due to the deposition of mineral water springs, travertine is the main Quaternary sediments around the springs. Water samples were collected from Toptapan mineral spring and Lighvan hot spring in July (dry season). The sampling method was according to standard methods for geochemical analysis. Field parameters such as PH, temperature, and EC were measured in situ, and samples were analyzed by ICP-OEC and ICP-MS in the laboratory of the Geological Survey of Iran. The measuring data showed that pH varies between 6.1 to 6.4. The surface temperature varies from 20.1˚C to 32.8˚C. The concentration of anions and cations in the Piper diagram show calcic bicarbonate type for Toptapan mineral spring and sodic bicarbonate type for Lighvan hot spring respectively. According to Lunglier – Ludwig diagram, the dissolution of carbonate and silicate minerals is the most important factor in increasing calcic cation. The Cl-Li-B diagram shows that the dissolution of sodic minerals and clays and ionic exchange are also the most important factors for increasing sodium in these springs. These data are in agreement to the host rocks, their mineralogy and their chemical composition. Based on the Ca-Mg-K geothermometer diagram, the geothermal reservoir temperature for Lighvan hot spring is 95-100 ˚C with a depth of about 2Km and for Toptapan mineral spring is 65-85 ˚C with a depth of less than 1Km. Also, high concentrations of chlorine show a deep geothermal primary reservoir in the Lighvan hot spring. These geochemical data show that these cold and hot springs are not polluted and not harmful for environmental point of views.

In the present investigation, 41 soil samples were subjected to single step chemical partitioning to assess the lithogenic and non-lithogenic portions of metals in Tehran's soils. The share of various studied metals in the anthropogenic portion ranges from as low as 0.2% to as high as 85% of bulk concentration. Geo-accumulation index (Igeo) showed that Cd falls within "heavily contaminated" soils. It might be inferred that Ni, Cu, Cr, Zn, Co and Ca fall within "Deficient to minimal" class in accordance with enrichment factor (EF) classification.. Enrichment factor values (to some extents) match with the chemical partition studies results (except for Ni and Cr). The very low Ca content of soil samples could be indicative of low biological productivity in the Tehran's soil. Also the very low concentrations of Mn could be indicative of reducing environment in soils of Tehran.

Random and unscientific disposal of municipal waste is an important factor affecting the geotechnical characteristics and concentrations of heavy metals in the soil. Unconfined compressive strength, Atterberg limit, and maximum dry density tests were included. These tests were designed to determine the effects of open waste dumps on geotechnical properties and the concentration of heavy metals in the underlying open dump soil. Soil samples collected from the landfill at Al-Sayyahia Village, Babylon Governorate, showed changes in the rates of geotechnical properties evaluation, as the value of the confined compressive strength decreased by high rates from 54 to 22 kN/m2. As well, when comparing the maximum values of dry density of samples from the control site, neighboring the landfill, the average value decreased from 1.91 to 1.74 gm/cm3. Chemical tests revealed that the pH and organic matter percentages in the open dump soil samples were significantly higher than in the control site. These percentages ranged from 9.67% and 2.542% to 7.4% and 0.215%, respectively. In addition, the average value of electrical conductivity was 5.6 mS/cm in the open dump soil, whereas in the control site was 3.6 mS/cm. Iron, lead, Copper, Nickel, Chrome, Zinc, Cadmium, and Arsenic have average concentrations of 4.64%, 14.02, 44.86, 236.36, 278.36, 95.26, 2.034, and 13.84 ppm, respectively. They are higher at open landfill sites than in control site samples.

Evaluation of the geochemistry and hydrochemical quality of Bam salt dome located in southern Iran, was conducted in this study. Two composite samples from salt units were collected and analysed by XRD and XRF to determine their mineral and elemental compositions. Water samples were also collected from the only spring in the area and analysed for major anions, cations and some toxic elements. The results indicated halite as the major mineral present, while quartz, anhydrite and dolomite were present at minor levels. The presence of anhydrite and dolomite together with quartz had negative effects on edible salt quality. The dominant water type in the area was sodium-chloride. Negligible sulphate and calcium contents may be attributed to anhydrites detected in the geological texture of the study area. According to a Schoeller diagram, the water is not suitable for drinking. Concentrations of toxic metals in the salt sample were significantly higher than those in water samples. Such a result can be viewed as an opportunity to produce edible salts from the evaporation of spring water.

Solid-solution partitioning of Rare Earth Elements in mine-tailings and soils in China: experimental results and multi-surface modelling. Interfaces Against Pollution

The migration of uranium from polluted soil has been investigated in the field, and through modelling of thermodynamics and kinetics of uranium-water-rock interactions. Field monitoring following surface contamination by uranium deposits revealed up to 5 m deep uranium migration in soil and chalk substrate, as well as uranium concentrations in groundwater significantly higher than the geochemical background. Such observations can hardly be explained by a pure reactive transport dominated by reversible adsorption of uranium onto mineral phases. Therefore, a reactive transport model using the HYTEC code has been developed to better assess uranium migration through soil to the carbonate aquifer. Reactive transport modelling shows that adsorption of U (VI) at equilibrium on goethite at pH 7 is responsible for strong immobilization of uranium in the soil and carbonate matrix, matching uranium concentration profiles observed in boreholes. Simulations considering highly mobile ternary complex Ca2UO2(CO3)3(aq) in the aqueous phase cannot account alone for the rapid migration of uranium through the unsaturated zone. Without a mobile colloidal phase, the model clearly underestimates the concentration of aqueous U(VI) that reached groundwater underneath polluted soils.

To understand the possible influence of the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident on the deep sea, as well as the geochemical behavior and transport of radionuclides, ¹³⁴Cs, ¹³⁷Cs, ²³⁹, ²⁴⁰Pu, ²⁴¹Pu, and ²³⁷Np were measured in the abyssal sediments of the Northwest Pacific (NWP) and Central Equatorial Pacific (CEP) Ocean. Data on the characteristics of these sediments obtained after the FDNPP accident are extremely rare, especially in the NWP subtropical gyre (NPSG) region. FDNPP-derived radio-Cs (¹³⁴Cs, ¹³⁷Cs) arrived at the open sea floor of the NWP before 2018 but was only found in the Kuroshio-Oyashio Extension (KOE) region. No FDNPP-derived Pu was detected in the abyssal sediments of the NWP or CEP. Pu in the NWP mainly originated from global fallout and the Pacific Proving Ground (PPG) close-in fallout, except for at station WP1 (39°N in the KOE region), where an abnormal but non-FDNPP-derived Pu signal was detected. Pu in the eastern CEP sediment was less affected by the PPG close-in fallout from the Marshall Islands and was mainly derived from global fallout, with some close-in fallout from the Johnston Atoll test. The KOE region was the area most affected by PPG close-in fallout Pu via Kuroshio transport, while the lowest inventories of ²³⁹⁺²⁴⁰Pu and ²³⁷Np were found in the NPSG region due to its oligotrophic environment. The ²³⁷Np originated from the same source as Pu, and the latitudinal pattern of ²³⁷Np was consistent with that of Pu. Station SS (in the marginal sea of the NWP) contained high ²³⁷Np/²³⁹Pu atom ratios in the deeper layers of sediment and had a ²³⁷Np depth profile opposite that of the ²³⁹⁺²⁴⁰Pu profile, compared to other stations; these differences are mainly attributed to differences in the behaviors of ²³⁷Np and ²³⁹Pu.

The main objective of this study was to investigate the 2019 and 2022 oil spill events that occurred off the coast of the State of Ceará, Northeastern Brazil. To further assess these mysterious oil spills, we investigated whether the oils stranded on the beaches of Ceará in 2019 and 2022 had the same origin, whether their compositional differences were due to weathering processes, and whether the materials from both were natural or industrially processed. We collected oil samples in October 2019 and January 2022, soon after their appearance on the beaches. We applied a forensic environmental geochemistry approach using both one-dimensional and two-dimensional gas chromatography to assess chemical composition. The collected material had characteristics of crude oil and not refined oils. In addition, the 2022 oil samples collected over 130 km of the east coast of Ceará had a similar chemical profile and were thus considered to originate from the same source. However, these oils had distinct biomarker profiles compared to those of the 2019 oils, including resistant terpanes and triaromatic steranes, thus excluding the hypothesis that the oil that reached the coast of Ceará in January 2022 is related to the tragedy that occurred in 2019. From a geochemical perspective, the oil released in 2019 is more thermally mature than that released in 2022, with both having source rocks with distinct types of organic matter and depositional environments. As the coast of Ceará has vast ecological diversity and Marine Protected Areas, the possibility of occasional oil spills in the area causing severe environmental pollution should be investigated from multiple perspectives, including forensic environmental geochemistry.

Acid mine drainage (AMD) is generated by the bio-oxidation of sulfide minerals. To understand the AMD formation and evolution, it is necessary to determine the composition and variation of acidophilic community, and their role in AMD ecosystem. In this study, we compared seasonal variations of geochemistry and microbial composition of two adjacent AMD lakes with different formation histories in Anhui Province, China. Lake Paitu (PT) formed in 1970s near a mine dump and the pH was in the range of 3.01–3.16, with the lowest in spring and summer while the highest in winter. The main ions in PT were Al and SO₄²⁻, whereas Fe concentration was relatively low. The concentrations of these ions were the lowest in summer and the highest in winter. Lake Tafang (TF) formed in around 2013 in a pit was more acidic (pH 2.43–2.75), but the seasonal variation of pH was the same as PT. Compared with Lake PT, TF had higher Fe, lower Al and SO₄²⁻ concentrations, and showed no significant seasonal changes. Despite salient seasonal variations of prokaryotic composition in Lake PT, Ferrovum was the major iron-oxidizing bacterium in most seasons. Furthermore, Lake PT was also rich in heterotrophic bacteria (48.6 ± 15.9%). Both prokaryotic diversity and evenness of Lake TF were lower than PT, and chemolithotrophic iron-oxidizing bacteria (71.7 ± 25.4%) were dominant in almost all samples. Besides Ferrovum, more acid tolerant iron-oxidizer Leptospirillum and Acidithiobacillus were also abundant in Lake TF. Chlamydomonas was the major eukaryote in Lake PT and it flourished repeatedly at the end of December, causing an extremely high chlorophyll a concentration (587 μg/L) at one sampling site in 2016, which provided rich nutrients for heterotrophic bacteria. The main alga in Lake TF was Chrysonebula, but its concentration was low, apparently because of the strong acidity and dark red color of lake water.