Organic matter, as an electron donor, plays a vital role in As mobilization mediated by microorganisms during reductive dissolution of Fe/Mn oxides in shallow aquifers. However, the specific types and sources of organic matter involved in biogeochemical processes accelerating As mobilization are still controversial. Both sediment and groundwater samples were collected at different depths from aquifers of the Hetao Basin, a typical inland basin hosting high As groundwater. Sedimentary lipids and their compound-specific carbon isotope ratios were analyzed to evaluate characteristics and sources of organic matter. Results show that sedimentary As were well correlated with Fe and Mn oxides, suggesting that As exist as Fe/Mn oxide bound forms. Groundwater As far exceeded the drinking water guide value of 10 μg/L. Moreover, As concentrations in shallow groundwater were relatively higher. Lipids in clay were mainly originated from terrestrial higher plants, while that in fine sand samples were derived from terrestrial higher plants, microorganism and petroleum. Shallow fine sand samples were also characterized by evident in-situ biodegradation. Compound-specific carbon isotope compositions of sedimentary lipids showed that short-chain n-alkanes and n-alkanoic acids had more positive δ13C values compared to long-chain compounds, especially in shallow fine sand samples. δ13CTOC were also low in shallow fine sand samples. These results jointly indicate that these lipids in shallow fine sand samples acted as carbon source for indigenous microorganism and the short-chain components were particularly more vulnerable to biodegradation, which may contribute to high As concentrations in shallow groundwater. The new findings provide the first evidence that short chain length n-alkyl compounds afforded a source of potential electron donors for microbially mediated As mobilization process in the shallow aquifers.

Since the introduction of standardized nematode toxicity assays by the American Society for Testing and Materials (ASTM) and International Organization for Standardization (ISO), many studies have reported their use. Given that the currently used standardized nematode toxicity assays have certain limitations, in this study, we examined the use of a novel nematode offspring counting assay for evaluating soil ecotoxicity based on a previous soil-agar isolation method used to recover live adult nematodes. In this new assay, adult Caenorhabditis elegans were exposed to soil using a standardized toxicity assay procedure, and the resulting offspring in test soils attracted by a microbial food source in agar plates were counted. This method differs from previously used assays in terms of its endpoint, namely, the number of nematode offspring. The applicability of the bioassay was demonstrated using metal-spiked soils, which revealed metal concentration-dependent responses, and with 36 field soil samples characterized by different physicochemical properties and containing various metals. Principal component analysis revealed that texture fraction (clay, sand, and silt) and electrical conductivity values were the main factors influencing the nematode offspring counting assay, and these findings warrant further investigation. The nematode offspring counting assay is a rapid and simple process that can provide multi-directional toxicity assessment when used in conjunction with other standard methods.

This study is the first quantitative report on petroleum biomarkers from the coral reefs systems of the Persian Gulf. 120 reef surface sediment samples from ten fragile coral reef ecosystems were collected and analyzed for grain size, biogenic elements, elemental ratios, and petroleum biomarkers (n-alkanes, PAHs¹ and Hopanes) to assess the sources and early diagenesis of sedimentary organic matter. The mean grain size of the reef sediments ranged from 13.56 to 37.11% (Clay), 26.92 to 51.73% (Sand) and 35.97 to 43.85% (Silt). TOC² (3.35–9.72 mg.g⁻¹) and TON³ (0.4–1.10 mg.g⁻¹) were identified as influencing factors on the accumulation of petroleum hydrocarbons, whilst BC⁴ (1.08–3.28 mg.g⁻¹) and TIN⁵ (0.13–0.86) did not exhibit any determining effect. Although BC and TIN demonstrated heterogeneous spatial distribution, TOC and TON indicated homogenous distribution with continually upward trend in concentration from the east to west ward of the Gulf. The mean calculated TOC/TN ratios vacillated according to the stations (p < 0.05) from 2.96 at Shidvar Island to 8.64 at Hengam Island. The high TOC/TN ratios were observed in the Hengam (8.64), Kharg (8.04) and Siri (6.29), respectively, suggesting a predominant marine origin. The mean concentrations of ∑C11–35n-alkanes, ∑30 PAHs and ∑9Hopanes were found in the ranges of 385–937 μg.g⁻¹dw, (overall mean:590 μg.g⁻¹dw), 326–793 ng.g⁻¹dw (499 ng.g⁻¹dw), 88 to 568 ng.g⁻¹ d (258 ng.g⁻¹dw), respectively. Higher concentrations of detected petroleum biomarkers in reef sediments were chiefly distributed near main industrial areas, Kharg, Lavan and Siri, whilst the lower concentrations were in Hormoz and Qeshm. In addition, one-way ANOVA⁶ analysis demonstrated considerably significant differences (p < 0.05) among concentration of detected total petroleum hydrocarbons between most sampling locations. Some sampling sites especially Kharg, Lavan, Siri and Lark indicated higher concentration of n-alkanes due to the higher maintenance of organic matter by high clay content in the sediments. Furthermore, most sediment samples, except for Hormoz, Qeshm and Hengam showed an even carbon preference for n-alkanes which could be correlated to bacterial input. NPMDS⁷ analysis also demonstrated that among the congeners of petroleum biomarkers, n-C12,n-C14, n-C16,n-C18 and n-C20 for n-alkanes, Phe⁸ and Naph⁹ along with their Alkyl homologues for PAHs (2–3 rings accounted for 60%) and C30αβ and C29αβ for Hopanes were discriminated from their other congeners in the whole study area. Our results based on the PCA¹⁰ analysis and diagnostic indices of AHs¹¹ and PAHs along with ring classification of PAHs, in addition, the ubiquitous presence of UCM,¹² and Hopanes revealed that the main sources of the pollution were petroleum and petroleum combustion mainly from offshore oil exploration and extraction, discharge of pollutants from shipping activities.

Glyphosate is one of the most used herbicides in agricultural lands worldwide. Wind-eroded sediment and dust, as an environmental transport pathway of glyphosate and of its main metabolite aminomethylphosphonic acid (AMPA), can result in environmental- and human exposure far beyond the agricultural areas where it has been applied. Therefore, special attention is required to the airborne transport of glyphosate and AMPA. In this study, we investigated the behavior of glyphosate and AMPA in wind-eroded sediment by measuring their content in different size fractions (median diameters between 715 and 8 μm) of a loess soil, during a period of 28 days after glyphosate application. Granulometrical extraction was done using a wind tunnel and a Soil Fine Particle Extractor. Extractions were conducted on days 0, 3, 7, 14, 21 and 28 after glyphosate application. Results indicated that glyphosate and AMPA contents were significantly higher in the finest particle fractions (median diameters between 8 and 18 μm), and lowered significantly with the increase in particle size. However, their content remained constant when aggregates were present in the sample. Glyphosate and AMPA contents correlated positively with clay, organic matter, and silt content. The dissipation of glyphosate over time was very low, which was most probably due to the low soil moisture content of the sediment. Consequently, the formation of AMPA was also very low. The low dissipation of glyphosate in our study indicates that the risk of glyphosate transport in dry sediment to off-target areas by wind can be very high. The highest glyphosate and AMPA contents were found in the smallest soil fractions (PM10 and less), which are easily inhaled and, therefore, contribute to human exposure.

Addressing the challenge that phosphorus is the key factor and cause for eutrophication, we evaluated the phosphorus release control performance of a new phosphorus inactive clay (PIC) and compared with Phoslock®. Meanwhile, the impacts of PIC and Phoslock® on phytoplankton abundance and community structure in eutrophic water were also discussed. With the dosage of 40 mg/L, PIC effectively removed 97.7% of total phosphorus (TP) and 98.3% of soluble reactive phosphorus (SRP) in eutrophic waters. In sediments, Fe/Al-phosphorus and organic phosphorus remained stable whereas Ca-phosphorus had a significant increase of 13.1%. The results indicated that PIC may form the active overlay at water-sediment interface and decrease the bioavailability of phosphorus. The phytoplankton abundance was significantly reduced by PIC and decreased from (1.0–2.4) × 107 cells/L to (1.3–4.3) × 106 cells/L after 15 d simultaneous experiment. The phytoplankton community structure was also altered, where Cyanobacteria and Bacillariophyceae were the most inhibited and less dominant due to their sensitivity to phosphorus. After PIC treatment, the residual lanthanum concentration in water was 1.44–3.79 μg/L, and the residual aluminium concentration was low as 101.26–103.72 μg/L, which was much less than the recommended concentration of 200 μg/L. This study suggests that PIC is an appropriate material for phosphorus inactivation and algal bloom control, meaning its huge potential application in eutrophication restoration and management.

Uptake and elimination kinetics of metals in soil invertebrates are a function of both soil and organism properties. This study critically reviewed metal toxicokinetics in soil invertebrates and its potential use for assessing bioavailability. Uptake and elimination rate constants of different metals are summarized. Invertebrates have different strategies for essential and non-essential metals. As a consequence, different types of models must be applied to describe metal uptake and elimination kinetics. We discuss model parameters for each metal separately and show how they are influenced by exposure concentrations and by physiological properties of the organisms. Soil pH, cation exchange capacity, clay and organic matter content significantly affect uptake rates of non-essential metals in soil invertebrates. For essential metals, kinetics is hardly influenced by soil properties, but rather prone to physiological regulation mechanisms of the organisms. Our analysis illustrates that toxicokinetics can be a valuable measurement to assess bioavailability of soil-bound metals.

Green tides dominated by Ulva prolifera have be present in the Southern Yellow Sea for 15 consecutive years. They not only damage the marine environment, but also cause economic losses to coastal cities. However, there is still no fully effective approach for preventing green tides. In this article, approaches for the prevention of U. prolifera taken over recent years are reviewed. They can be generally divided into physical, chemical, and biological approaches. Physical approaches have been used to control the overwhelming green macroalgae bloom and inhibit the germination of U. prolifera, including physical salvage approach, refrigeration net technology, improved farming methods and raft technology, and modified clay method. These approaches require significant labor and material resources. Many chemical reagents have been used to eliminate U. prolifera early germination and growth, such as oxidative algaecide, acid treatment, heavy metal compounds, antifouling coating, and alkaloids. Chemical approaches have high efficiency, high economic benefit, and simple operation. Presently, biological control approaches remain in the exploratory stage. The verification of pilot and large-scale experiment results in sea areas is lacking, including the application of large organisms and microorganisms to control U. prolifera, and some of the mechanisms have not been thoroughly studied. This article introduces the three types of approaches, and evaluates the advantages and disadvantages of different methods to facilitate the reduction of the green tide bloom scale in the Southern Yellow Sea.

This study assesses for the first time the concentrations of microplastics (MPs) in sediments, water and two human-consumed mussels with different ecological traits (Amarilladesma mactroides and Brachidontes rodriguezii) in a touristic sandy beach of Argentina. MPs were characterized through FTIR and SEM/EDX techniques. All the samples presented MPs with similar concentrations as other human-impacted coastal areas of the world, being black and blue fibers of < 0.5 and 0.5-1 mm the most abundant. SEM images exhibited cracks and fractures with clay minerals and microorganisms adhered to MPs surface. EDX spectrums showed potentially toxic elements, such as Cr, Ti, and Mo. FTIR identified polymers such as cellulose, polyamides, and polyacrylates in most of the samples analyzed. Our study demonstrates that microplastic pollution is a common threat to sandy beaches in Argentina, worsened by plastic particles carrying metal ions with potential toxic effects to the biota, including A. mactroides, an endangered species.

PURPOSE OF REVIEW: This review provides an overview of the latest developments in immobilisation of per- and poly-fluoroalkyl substances (PFAS) for soil remediation. It examines the efficacy of a range of amendments, including those with binding agents, along with a discussion of immobilisation mechanisms and post-immobilisation assessment needs. RECENT FINDINGS: Researchers have recently applied a variety of soil amendments to soil for PFAS immobilisation. Efficacy of these has varied widely, both between amendment and soil types and for individual PFAS molecules present in contaminated soils. Activated carbon based amendments, including composite amendments exhibit the highest efficacies of the examined studies. Immobilisation of PFAS is complex, with efficacy of immobilisation varying with soil properties including pH, clay and organic matter content, amendment properties, and molecular properties of the individual PFAS. Optimal remediation strategies need to be adjusted accordingly to site specific soil properties and contamination profiles. Additionally, bioavailability testing needs to supplement standard leaching approaches to determine effectiveness of PFAS soil immobilisation strategies.

The focus of this study was to determine the depth-wise variability of physicochemical properties (i.e., pH, TOC, TN, and EC), and heavy metals (i.e., Pb, Cu, Zn, As, and Cr) concentration, and the associated biological and ecological risks of the mangrove sediment. The accumulation of metal contents and the phytoremediation and phytoextraction were also investigated in a mangrove species, Acanthus ilicifolius. The mangrove sediment consists of a higher proportion of sand fraction (56.6–74.7%) followed by clay (10–28%) and silt (10.1–15. 7%) fractions. The concentrations (mg/kg) of Pb, Cu, Zn, As, and Cr were ranged from 22.05–34.3, 8.58–22.77, 85.07–114, 5.56–12.91, and 0.98–5.12 in all the sediment layers. The hierarchy of the mean metal concentration in sediment was Zn (102 mg/kg) > Pb (25.6 mg/kg) > Cu (14.8 mg/kg) > As (8.79 mg/kg) > Cr (2.74 mg/kg) respectively. The examined metal concentrations were below the respective average shale values (ASVs). The degree of environmental, ecological, and biological risks was minimal according to various pollution indices like geoaccumulation index (Igₑₒ), contamination factor (CF), and pollution load index (PLI). According to sediment quality guidelines (SQGs), the adverse biological risk effect was not likely to occur. The result of the potential ecological risk index (PERI) demonstrated that the study area was in the low-risk condition as the corresponded RI value < 100. A combined influence of geogenic and anthropogenic factors was identified as the metal sources by multivariate analysis. The study found that the accumulation rate of the metal contents was higher in leaves than that of roots. The mean descending metal concentration values were Zn (107) > Pb (28. 7) > Cu (16.9) > As (11.2) > Cr (4.99) in leaves and Zn (104.32) > Pb (27.02) > Cu (15.29) > As (10.39) > Cr (3.80) in roots. The translocation and bioaccumulation factors of heavy metals suggested that the mangrove plant species, A. ilicifolius can be used for phytoremediation and phytoextraction since the bio-concentration factor and translocation factor > 1. The studied species exhibited the metal tolerance associated with two following strategies, metal exclusion, and metal accumulation. However, excess metal tolerance can impact the surrounding marine environment.