Microplastics pollution has become a matter of global concern because of its effects on aquatic life and the ecosystem. This study investigated the abundance and types of microplastics found in an urban canal of Thailand. Water quality and the relationship between microplastics pollutants and the physicochemical properties of water quality were also analyzed to provide evidence for this study. The mean abundance of microplastics was 370 ± 140 particle(p)/m3. The highest number and concentration of microplastics were found on surface water corelated with urbanization. Transparent brown and transparent colors in the form of film and fiber/lines were the predominant morphology. Polypropylene (PP) and polyethylene (PE) were the most abundant polymer type in all surface water samples. Furthermore, water quality was related with microplastic pollution. The physicochemical properties of turbidity (0.99), conductivity (0.97), total solid (0.95) and biological oxygen demand (0.84) were accounted for greatest influences on microplastics distribution. The estimated equation of microplastics was also closely corelated with water quality. These results demonstrate that microplastic pollution has progressed more in poor water quality than good water quality, indicating that the inflow process and sources of microplastics are similar to those of other pollutants. Therefore, this study is expected to encourage and enforce solid waste and wastewater management policies that prevent microplastics pollution in the environment.

Phenols have attracted global interest in the sphere of environmental management due to their potential toxicity on human health. This study determined concentrations of three priority phenolic compounds in effluent and water of a local textile industry in Abeokuta, Nigeria.  During tie-dye production, triplicates of effluent, well water, stream and control water were collected three times from five points to give a total of forty-five samples. Physicochemical parameters of samples including temperature, pH, electrical conductivity (EC), total suspended solids (TSS) and total dissolved solids (TDS) were determined according to standard methods while the concentrations of the priority phenolic compounds (4-nitrophenol, 4-chloro-3-methylphenol and 2, 4-dinitrophenol) were determined using High Performance Liquid Chromatography equipped with Ultra-Violet detector (HPLC/UV). Data obtained were subjected to descriptive (mean and standard deviation) and inferential (ANOVA) statistics. pH, EC and TSS of effluent and water samples were higher than the permissible limits of World Health Organization (WHO) and Federal Environmental Protection Agency (FEPA) while temperature of the effluent samples and TDS of the well water samples were within standard values. Higher concentrations of the priority phenolic compounds occurred in effluent than water samples but 4-nitrophenol was below detection limit (DL) in water samples. Concentrations of 4-nitrophenol, 4-chloro-3-methylphenol and 2,4-dinitrophenol in effluent exceeded stipulated standard of WHO (0.01 mg/L) and water samples. High concentrations of phenols in water bodies at the local textile industry suggest uncontrolled discharge of effluent from the industry which could eventually reach surface and ground water with potential significant health implications to the populace.

Severodvinsk city is the largest industrial center for the construction and repair of naval vessels in the NW Russia. The purpose of the presented study was to identify the main sources of pollution of the Severodvinsk industrial region and assess the ecological situation based on analysis of toxic metals in water and snow. Heavy metals content in water, melt snow filtrate and solid residue was measured using ICP-MS. On the urban area, there were high concentrations of Fe (up to 2843 MPC) in soluble form of snow, Al (up to 4680 MPC), Fe (up to 2807 MPC), Ni (up to 66.5 MPC), Pb (up to 44.7 MPC), Cd (up to 43.3 MPC), Cr (up to 43.2 MPC), Mn (up to 13.3 MPC), Co (up to 7.3 MPC), and As (up to 3.4 MPC) in insoluble form of snow, Fe (up to 56213 MPC) in water from wells. There were high values of mineralization (598 mg/L) and low pH values (to 5.21) in sites most susceptible to anthropogenic pollution. Statistical analysis showed that most of the metals in snow cover were linked with each other by strong correlation (r>0.9). Calculation of toxicological indices HMEI, HMPI, HMTL, HI and CR showed extremely high and dangerous for public health level of heavy metal pollution in the Severodvinsk industrial district. Studied radiation parameters of water from wells were within acceptable limits. Results obtained indicate the need to change the type of fuel in thermal power plant and reduce toxic emissions from the shipbuilding enterprises.

As a common natural phenomenon, corpse decomposition may lead to serious environmental pollution such as nitrogen pollution. However, less is known about antibiotic resistance genes (ARGs), an emerging contaminant, during corpse degradation. Here, ARGs and microbiome in three soil types (black, red and yellow soil) have been investigated between experimental and control groups based on next-generation sequencing and high-throughput quantitative PCR techniques. We found that the absolute abundance of total ARGs and mobile genetic elements (MGEs) in the experimental groups were respectively enriched 536.96 and 240.60 times in different soil types, and the number of ARGs in experimental groups was 7–25 more than that in control groups. For experimental groups, the distribution of ARGs was distinct in different soil types, but sulfonamide resistance genes were always enriched. Corpse decomposition was a primary determinant for ARGs profiles. Microbiome, NH₄⁺ concentrates and pH also significantly affected ARGs profiles. Nevertheless, soil types had few effects on ARGs. For soil microbiome, some genera were elevated in experimental groups such as the Ignatzschineria and Myroides. The alpha diversity is decreased in experimental groups and microbial community structures are different between treatments. Additionally, the Escherichia and Neisseria were potential pathogens elevated in experimental groups. Network analysis indicated that most of ARGs like sulfonamide and multidrug resistance genes presented strong positively correlations with NH₄⁺ concentrates and pH, and some genera like Ignatzschineria and Dysgonomonas were positively correlated with several ARGs such as aminoglycoside and sulfonamide resistance genes. Our study reveals a law of ARGs’ enrichment markedly during corpse decomposing in different soil types, and these ARGs contaminant maintaining in environment may pose a potential threat to environmental safety and human health.

Rice is the world’s most consumed and in-demand grain. Ecuador is one of the main rice-consuming countries in Latin America, with an average per capita consumption of 53.2 kg per year. Rice cultivation takes place under flooding conditions, which favors the mobilization and subsequent accumulation of heavy metals in the plant. This study’s principal objective was to evaluate the contamination of cadmium (Cd) and lead (Pb) in the rice cultivation system in the province of Guayas. To this end, extensive sampling of water, soil and rice grains was carried. Water samples were analyzed to determine physicochemical properties and concentrations of dissolved Cd and Pb. Physicochemical properties, total organic carbon (TOC), total content of nitrogen (N), iron (Fe), manganese (Mn), phosphorus (P), bioavailable phosphorus (P mehlich), Cd and Pb were determined in soil samples. In addition, to understand the dynamics of Cd and Pb mobility and bioavailability, an extraction of six randomly selected soil samples was carried out. The concentration values of the total Cd and Pb content in the rice cultivation system did not exceed the maximum recommended limit for soil, water and rice grains. However, 85% of the total Cd was in the soluble or exchangeable fraction of the soil, while the Pb was strongly bound to crystalline iron oxyhydroxides. It was established that the TOC, N, Fe, and P mehlich have a significant correlation (p < 0.05) with the overall concentration of Cd and Pb in the rice farming soil. The Cd and Pb present in rice do not represent a dietary health risk to the population of Ecuador.

Despite the mercury (Hg) control measures adopted by the international community, Hg still poses a significant risk to ecosystem and human health. This is primarily due to the ability of atmospheric Hg to travel intercontinentally and contaminating terrestrial and aquatic environments far from its natural and anthropogenic point sources. The issue of Hg pollution is further complicated by its unique physicochemical characteristics, most noticeably its multiple chemical forms that vary in their toxicity and environmental mobility. This meant that most of the risk evaluation protocols developed for other metal(loid)s are not suitable for Hg. Soil is a major reservoir of Hg and a key player in its global cycle. To fully assess the risks of soil Hg it is essential to estimate its bioavailability and/or availability which are closely linked to its toxicity. However, the accurate determination of the (bio)-available pools of Hg in soils is problematic, because the terms ‘bioavailable’ and ‘available’ are ill-defined. In particular, the term ‘bioavailable pool’, representing the fraction of Hg that is accessible to living organisms, has been consistently misused by interchanging with other intrinsically different terms e.g. mobile, labile, reactive and soluble pools. A wide array of physical, chemical, biological and isotopic exchange methods were developed to estimate the (bio)-available pools of Hg in soil in an attempt to offer a plausible assessment of its risks. Unfortunately, many of these methods do not mirror the (bio)-available pools of soil Hg and suffer from technical drawbacks. In this review, we discuss advantages and disadvantages of methods that are currently applied to quantify the (bio)-availability of Hg in soils. We recommended the most feasible methods and give suggestions how to improve the determination of (bio)-available Hg in soils.

Despite their ecological and socioeconomic importance, mangroves are among the most threatened tropical environments in the world. In the past two decades, the world's mangrove degradation and loss were estimated to lie between an 35% and >80%. However, appropriate bioindicators for assessing the impact of external factors, and for differentiating polluted from unpolluted areas are still scarce. Here, we determine the physicochemical profiles of the soils of two mangroves, one exposed to and one not exposed to anthropogenic factors. By metagenomic analysis based on 16S rRNA, we generated the bacterial diversity profiles of the soils and estimated their functional profiles. Our results showed that the two examined mangrove forests differed significantly in the physicochemical properties of the soils, especially regarding organic carbon, phosphorus and metal content, as well as in their microbial communities, which was likely caused by anthropogenic pollution. The physicochemical differences between the soils explained 76% of the differential bacterial composition, and 64% depended solely on gradients of phosphorus, metal ions and potassium. We found two genera JL-ETNP-Z39 and TA06 exclusively in polluted and non-polluted mangroves, respectively. Additionally, the polluted mangrove was enriched in Gemmatimonadetes, Cyanobacteria, Chloroflexi, Firmicutes, Acidobacteria, and Nitrospirae. A total of 77 genera were affected by anthropic contamination, of which we propose 33 as bioindicators; 26 enriched, and 7 depleted upon pollution.

Nitrogen (N) addition can change physicochemical properties and biogeochemical processes in soil, but whether or not these changes further affect the transport and transformation of heavy metal speciation is unknown. Here, a long-term (2004–2016) field experiment was conducted to assess the responses of different heavy metal speciation in three soil aggregate fractions to N additions in a temperate agroecosystem of North China. The organic matter turnover time was quantified based on changes in δ13C following the conversion from C3 (wheat) to C4 crop (corn). Averagely, N addition decreases and increases the heavy metal contents in bioavailable and organic bound fractions by 27.5% and 16.6%, respectively, suggesting N addition promotes the transformation of heavy metal speciation from bioavailable to organic bound, and such a promotion in a small aggregate fraction is more remarkable than that in a large aggregate fraction. The transformations of heavy metal speciation from bioavailable to organic bound in all soil aggregate fractions are largely dependent on the increments in the turnover time of organic matter. The increase in organic matter turnover time induced by N addition may inhibit the desorption of heavy metals from organic matter by prolonging the interaction time between heavy metals and organic matter and enhance the capacity of organic matter to adsorb heavy metals by increasing the humification degree and functional group. Our work can provide insights into the accumulation, migration, and transformation of heavy metals in soils in the context of increasing global soil N input from a microenvironmental perspective.

Nanoplastics have attracted increasing attention in recent years due to their widespread existence in the environment and the potential adverse effects on living organisms. In this paper, the toxic effects of nanoplastics on organisms were systematically reviewed. The translocation and absorption of nanoplastics, as well as the release of additives and contaminants adsorbed on nanoplastics in the organism body were discussed, and the potential adverse effects of nanoplastics on human health were evaluated. Nanoplastics can be ingested by organisms, be accumulated in their body and be transferred along the food chains. Nanoplastics showed effects on the growth, development and reproduction of organisms, and disturbing the normal metabolism. The toxic effects on living organisms mainly depended on the surface chemical properties and the particle size of nanoplastics. Positively charged nanoplastics showed more significant effects on the normal physiological activity of cells than negatively charged nanoplastics, and smaller particle sized nanoplastics could more easily penetrate the cell membranes, hence, accumulated in tissues and cells. Additionally, the release of additives and contaminants adsorbed on nanoplastics in organism body poses more significant threats to organisms than nanoplastics themselves. However, there are still knowledge gaps in the determination and quantification of nanoplastics, as well as their contaminant release mechanisms, degradation rates and process from large plastics to nanoplastics, and the transportation of nanoplastics along food chains. These challenges would hinder the risk assessment of nanoplastics in the environment. It is necessary to further develop the risk assessment of nanoplastics and deeply investigate its toxicological effects.

Tributyl phosphate (TBP) is recognised as a global environmental contaminant because of its wide use in floatation reagents, nuclear fuel reprocessing and plasticisers. This contaminant is hardly degraded by hydrolysis in the environment due to its special physicochemical properties. In this study, one TBP-degrading strain was isolated from TBP-contaminated abandoned mine tailings, and 16S rRNA identification revealed that the strain belonged to the genus Sphingomonas. Results validated that the strain could utilise TBP as the sole carbon source, and vitamin was not the essential factor for its growth. Liquid chromatography time-of-flight mass spectrometry analysis identified di-n-butyl phosphate (DnBP) and mono-n-butyl phosphate (MnBP) as the intermediate metabolites for TBP biodegradation. No obvious change in carbon and hydrogen isotope composition was observed in biodegradation processes (cell suspension and crude extract degradation), which indicated that the first irreversible bond cleavage did not involve carbon or hydrogen. Hence, the TBP degradation scheme by Sphingomonas sp. proposed that the first irreversible step of TBP transferred to DnBP would lead to PO bond cleavage. This study combined the identification of products and isotope fractionation in substrates to investigate the transformation mechanism, thereby providing an eco-friendly and cost-effective way for the in situ bioremediation of TBP-contaminated sites by the isolated TBP degradation strain.