Metals sequestered in coastal sediments are normally considered to be stable, but this investigation shows – somewhat surprisingly – that mercury concentrations in a previously contaminated area, Harboøre Tange, Denmark, have decreased since the 1980s. Mercury concentrations were determined in sediment and benthic biota and present values were compared to values in the 1980s and values from areas without known; history of mercury contamination. Concentrations in both the upper 20 cm of the sediments and; biota are considerably lower now compared to latest monitoring (1980s). Sediment.concentrations at most locations have decreased from the 100–300 ng Hg g⁻¹ dry weight (dw) level to levels below the Background Concentration (BC) of 50 ng Hg g⁻¹ dw defined by Oslo-Paris Convention for the Protection of the Marine Environment of the North-East Atlantic; some stations are at the 2–10 ng Hg g⁻¹ dw level characteristic of Danish coastal sediments with no known history of mercury contamination. Concentrations of mercury in the benthic biota along Harboøre Tange have also decreased since the 1980s but despite the lowered mercury concentrations in the sediments, concentrations in most samples of benthic invertebrate fauna still exceed those in uncontaminated coastal areas and also the Environmental Quality Standard (EQS) of 20 ng Hg g⁻¹ wet weight (≈100 ng Hg g⁻¹ dry weight) defined by the European Union’s Water Framework Directive. Concentration ranges in selected organisms are: (Harboøre Tange l980s/Harboøre Tange now/uncontaminated areas - given in ng Hg g⁻¹ dw): Periwinkles Littorina littorea 9000/150–450/55-77, blue mussels Mytilus edulis up to 9000/300–500/40–170, cockles Cerastoderma edule up to 8000/400–1200/200, brown shrimp Crangon crangon 700–2200/150-450/47, eelgrass Zostera marina up to 330/25–70/12. The present results - together with a literature review - show that a simple and straight forward relationship between the concentrations of mercury in sediment and benthic organisms does not necessarily exist.

This study reports comprehensive analysis of seasonal and inter-annual variations of aerosol properties (optical, physical and chemical) and radiative effects over Pokhara Valley in the foothills of central Himalayas in Nepal utilizing the high-quality multi-year columnar aerosol data observed recently from January 2010 to December 2017. This paper focusses on the seasonal and inter-annual variations of chemical (composition), and absorption properties of aerosols and their radiative effects. The single scattering albedo (SSA) either decreases as a function of wavelength or remains independent of wavelength. The seasonal mean aerosol absorption optical depth (AAOD) exhibits a behavior opposite to that of SSA. Carbonaceous aerosols (CA) dominate (≥60%) aerosol absorption during the whole year. Black carbon (BC) alone contributes >60% to AAODCA while brown carbon (BrC) shares the rest. The absorbing aerosol types are determined to be BC, and mixed (BC and dust) only. Dust as absorbing aerosol type is absent over the Himalayan foothills. The ARFSFC is ≥ -50 Wm⁻² except in monsoon almost every year. The ARFATM is ≥ 50 Wm⁻² during winter and pre-monsoon in all the years. ARFESFC, ARFETOA and ARFEATM follow a similar pattern as that of ARF. High values of ARFE at SFC, TOA and ATM (except during monsoon when values are slightly lower) suggest that aerosols are efficient in significantly modulating the incoming solar flux throughout the year. The annual average aerosol-induced atmospheric heating rate (HR) over Pokhara is nearly 1 K day⁻¹ every year during 8-year observation, and is highest in 2015 (∼2.5 K day⁻¹). The HR is about 1 K day⁻¹ or more over all the locations in IGP during the year. These quantitative results can be used as inputs in global/regional climate models to assess the climate impact of aerosols, including on regional temperature, hydrological cycle and melting of glaciers and snowfields in the region.

The current global coronavirus disease 2019 (COVID-19) pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been a tremendous public health challenge globally. While the respiratory transmission of SARS-CoV-2 has been established, evolving reports on the impact of the gastrointestinal system and the prolonged faecal shedding of SARS-CoV-2 show the likelihood of faecally mediated transmission. The increasing evidential presence of SARS-CoV-2 in wastewater and faecal material poses a significant public health threat which may potentiate global vulnerability to high risk of human exposure through environmental drivers especially in less developed countries. While extensively exploring the likelihood of faecally mediated SARS-CoV-2 transmission, infection control and prevention measures aimed at mitigating this pandemic should holistically include environmental drivers.

The occurrence of Active Pharmaceutical Ingredients (APIs) in the environment is becoming a major area of concern due to their undesirable effects on non-target organisms. This study investigated the occurrence and risk of contamination by five antibiotics and three antiretrovirals drugs in a fast-growing peri-urban area in Kenya, with inadequate sewer system coverage. Due to poor sewage connectivity and poorly designed decentralized systems, wastewater is directly released in open drains. Water and sediment samples were collected from open surface water drains, while wastewater samples were collected from centralized wastewater treatment plants (WWTP). Solid-phase extraction and ultrasonic-assisted extraction for the aqueous and sediment samples respectively were carried out and extracts analyzed by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) using isotopically labeled internal standards. APIs were observed with the detection frequency ranging from 36% to 100%. High mean concentrations of 48.7 μg L⁻¹, 108 μg L⁻¹, and 532 μg L⁻¹ were observed in surface drains for Lamivudine (3 TC), Sulfamethoxazole (SMX), Ciprofloxacin (CIP) respectively. Drain sediments also showed high concentrations of APIs ranging from 2.1 to 13,100 μg kg⁻¹. APIs in this study exceeded those observed in existing literature studies. JKUAT WWTP removal efficiencies varied from −90.68% to 72.67%. Total APIs emission load of the study area was 3550 mg d⁻¹ with WWTP effluent contributing higher loads (2620 mg d⁻¹) than surface water drains (640 mg d⁻¹). Zidovudine (ZDV), nevirapine (NVP), and trimethoprim (TMP) loads in drains, however, exceeded WWTP effluent. Low to high ecotoxicity risk of the individual APIs were observed to the aquatic environment, with high risks for the development of antibiotic resistance in microbiome as determined by the risk quotient (RQ) approach. Risk management through efficient wastewater collection, conveyance, and treatment is necessary to suppress the measured concentrations.

The demineralized fraction (DM), lipid-free fraction (LF), nonhydrolyzable organic carbon fraction (NHC), and black carbon (BC) were isolated from five marine surface sediments, and they were characterized by elemental analysis as well as CO₂ and N₂ adsorption techniques, respectively. The NHC fractions were characterized using advanced solid-state ¹³C nuclear magnetic resonance (NMR) and x-ray photoelectron spectroscopy (XPS). Then, the sorption isotherms of phenanthrene (Phen) and nonylphenol (NP) on all of the samples were investigated by a batch technique. The CO₂ micropore volumes were corrected for the outer specific surface areas (SSAs) by using the N₂-SSA. Significant correlations between the micropore-filling volumes of Phen and NP and the micropore volumes suggested that the micropore-filling mechanism dominated the Phen and NP sorption. Meanwhile, the (O + N)/C atomic ratios were negatively and significantly correlated with the sorption capacities of Phen and NP, indicating that the sedimentary organic matter (SOM) polarity also played a significant role in the sorption process. In addition, a strong linear correlation was demonstrated between the aromatic C and the sorption capacity of Phen for the NHC fractions. This study demonstrates the importance of the micropores, polarity, and aromaticity on the sorption processes of Phen and NP in the sediments.

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.

As the typical range of influence of oil spills surrounds urbanised and economically active areas, it is likely that fragile regions may not be part of the most vulnerable zones. This premise is remediated in this paper with the adoption of a vulnerability approach based on the integration of static and dynamic information, such as oil pollution susceptibility. Susceptibility is a poorly consolidated term and is often used as synonym for environmental sensitivity; it is considered here to be the distribution areas of oil slicks. To test the proposed approach, an integrated estimation of environmental vulnerability is carried out for an environmentally sensitive area in the south of Brazil by merging static data inherent to the medium with information of a dynamic nature related to trajectory, behaviour and the fate of oil at sea. Moreover, the oil pollution intensity and environmental sensitivity data in susceptible areas are addressed. Subsequently, the environmental vulnerability is estimated by integrating hazard maps, concentrations and losses of the mass of the oil slick, oil beaching time and the littoral sensitivity index hierarchy. Results will prove to be useful to highlight critical areas for which the highest levels of severity are expected, which can lead to improvements in decision-making processes to support oil-spill prevention, as well as improve response readiness, especially in developing countries that have historically under-protected their sensitive regions.

Naphthalene sulfonic acids (NSAs) are used extensively in industrial applications as dispersants in dyes, rubbers, and pesticides, and as anti-corrosive agents in coatings, gels, and sealants. This study examined the toxicity of three NSA congeners, barium dinonylnaphthalene sulfonate (BaDNS), calcium dinonylnaphthalene sulfonate (CaDNS), and dinonylnaphthalene disulfonic acid (DNDS), to two benthic species, Tubifex tubifex and Hyalella azteca. Two substrates with different levels of organic carbon (sediment [2%] and sand [0%]) were used in toxicity tests. Juvenile production was the most sensitive endpoint for T. tubifex: the 28-d EC50s were <18.2, 22.2, and 64.0 μg/g dw in sand and 281.3, 361.6, and 218.9 μg/g dw in sediment for BaDNS, CaDNS, and DNDS, respectively. The 28-d LC50s for H. azteca were similar among compounds: 115.3, 82.1, and 49.0 μg/g dry weight (dw) in sand, and 627.3, 757.9, and >188.5 μg/g dw in sediment, for BaDNS, CaDNS, and DNDS, respectively. However, when LC50s were estimated based on concentrations of NSAs measured in overlying water (which can be an important route of exposure for H. azteca), BaDNS and CaDNS were 3–4 orders of magnitude more toxic than DNDS. The NSAs examined were >3-fold more toxic when present in substrates with no organic carbon (e.g., sand) for all H. azteca endpoints where LC/EC50s could be calculated and for sublethal endpoints for T. tubifex. The organic carbon content of the sediment appears to have acted as a sink and reduced NSA toxicity by decreasing bioavailability. Environmental sediment samples were collected from 12 river sites across southern Ontario. The maximum concentration of CaDNS observed in sediment collected from this region was 2.8 μg/g dw in sediment with 2% organic carbon; 100-fold lower than the lowest EC10 in the current study.

Devon Great Consols (DGC) is a region in south west England where extensive mining for Cu, Sn and As took place in the nineteenth century. Because of its historical and geological significance, DGC has protected status and is part of the Cornwall and West Devon Mining Landscape UNESCO World Heritage Site. Recently, the region was opened up to the public with the construction or redevelopment of various trails, tracks and facilities for walking, cycling and field visits. We used portable x-ray fluorescence spectrometry to measure, in situ, the concentrations of As in soils and dusts in areas that are accessible to the public. Concentrations ranged from about 140 to 75,000 μg g⁻¹ (n = 98), and in all but one case exceeded a Category 4 Screening Level for park-type soil of 179 μg g⁻¹. Samples returned to the laboratory and fractionated to <63 μm were subjected to an in vitro assessment of both oral and inhalable bioaccessibility, with concentrations ranging from <10 to 25,500 μg g⁻¹ and dependent on the precise nature and origin of the sample and the physiological fluid applied. Concentrations of As in PM₁₀ collected along various transects of the region averaged over 30 ng m⁻³ compared with a typical concentration in UK air of <1 ng m⁻³. Calculations using default EPA and CLEA estimates and that factor in for bioaccessibility suggest a 6-h visit to the region results in exposure to As well in excess of that of minimum risk. The overall risk is exacerbated for frequent visitors to the region and for workers employed at the site. Based on our observations, we recommend that the remodelling or repurposing of historical mine sites require more stringent management and mitigation measures.

The prevalence of microplastic debris in aquatic ecosystems as a result of anthropogenic activity has received worldwide attention. Although extensive research has reported ubiquitous and directly adverse effects on organisms, only a few published studies have proposed the long-term ecological consequences. The research in this field still lacks a systematic overview of the toxic effects of microplastics and a coherent understanding of the potential ecological consequences. Here, we draw upon cross-disciplinary scientific research from recent decades to 1) seek to understand the correlation between the responses of organisms to microplastics and the potential ecological disturbances, 2) summarize the potential ecological consequences triggered by microplastics in aquatic environments, and 3) discuss the barriers to the understanding of microplastic toxicology. In this paper, the physiochemical characteristics and dynamic distribution of microplastics were related to the toxicological concerns about microplastic bioavailability and environmental perturbation. The extent of the ecological disturbances depends on how the ecotoxicity of microplastics is transferred and proliferated throughout an aquatic environment. Microplastics are prevalent; they interfere with nutrient productivity and cycling, cause physiological stress in organisms (e.g., behavioral alterations, immune responses, abnormal metabolism, and changes to energy budgets), and threaten the ecosystem composition and stability. By integrating the linkages among the toxicities that range from the erosion of individual species to the defective development of biological communities to the collapse of the ecosystem functioning, this review provides a bottom-up framework for future research to address the mechanisms underlying the toxicity of microplastics in aquatic environments and the substantial ecological consequences.