Despite of much evidence of trace metal pollution in the Pearl River Estuary (PRE), the seasonal dynamics of metal bioavailability as well as the potential impacts of metal pollution on the local marine organisms in this estuary is poorly understood. In the present study, the accumulation of trace metals and reproductive states of three populations of oyster Crassostrea hongkongensis, a keystone bivalve species in the PRE, were for the first time investigated throughout a one-year field study. Significant temporal fluctuations of metal accumulation were observed in the somatic tissues of oysters, suggesting seasonal variations of metal bioavailability in the PRE. A major feature of the seasonal variations was the increased levels of metal bioaccumulation in the summer season for the contaminated sites nearby the major river inlets. High riverine inputs accompanied by relatively lower salinity in summer may greatly contribute to such variations. Furthermore, oyster populations from two contaminated sites had a poor reproductive condition in comparison with the reference oyster population, as reflected by a significant decrease of gonad-somatic index (GSI) and gonad cover area (GCA), as well as an obvious change of sex ratios. Gonadal metal accumulation of Cu, Zn, Ni, Co and Pb in the contaminated oysters was much higher than that in the relatively uncontaminated oysters. Especially, the concentrations of these metals in the gonad during the breeding season had significantly negative correlations with the gonad condition indexes (GSI and GCA). Our results suggested strong seasonal fluctuations of bioavailability of trace metals in this highly contaminated estuary as well as an adverse effect of metal pollution on the reproduction of local oyster populations.

A sediment core was obtained from Moira Lake to study the legacy of contamination and remediation at the Deloro industrial site which includes 95-years of operations involving gold mining, mineral processing, and arsenic-based pesticide production resulting in high levels of arsenic, cobalt, and nickel. A timeline for the sediment core was established by ²¹⁰Pb dating and used to evaluate the geochemical record and the impact on primary production and subfossil cladocerans. In the early 1800s, there was an initial increase in the arsenic, cobalt and nickel concentrations due to industrial development. By the 1850s, the rate of enrichment increased due to the conglomeration of small-scale operations. In the 1960s, the concentrations of those metal(loid)s decreased following the cessation of the industrial activity at Deloro and the initiation of a clean-up effort. Primary production, inferred by chlorophyll-a concentrations, initially decreased as the metal(loid)s concentrations increased. This was followed by a recovery of the chlorophyll-a concentrations and further increases in production to higher levels than recorded prior to the Deloro years. Secondary production, inferred by cladoceran assemblage structure, was initially dominated by bosminids. The assemblage then changed to one dominated by chydorids and daphnids with the change occurring contemporaneous with the change in chlorophyll-a. However, the changes in primary and secondary production occurred during the period of accelerated metal(loid) enrichment, suggesting limited impact of contamination on primary and secondary producers. Loss on ignition results revealed that during the period of accelerated arsenic enrichment, the carbonate content of the sediments increased while the percent organic content decreased. This work contributes to ongoing research to establish the environmental legacy of historical industrial activities within complex ecosystems. Furthermore, the combination of geochemical (i.e. ²¹⁰Pb, ICP-OES, XANES) and ecological analysis provides a more complete picture of the complex interactions that have occurred in Moira Lake.

Magnetic properties of urban street dust can be used as a proxy of urban pollution. In this study, magnetic measurements on 160 street dust samples, collected from five different functional areas (industrial, traffic, commercial, residential and clean areas) in sixteen administrative districts in Shanghai, China, were systematically conducted. It is showed that magnetic carriers were predominately coarse-grain ferrimagnetic particles. Meantime, concentration-related magnetic parameters showed significant variations among the functional areas and administrative units. Magnetic susceptibility (χ) decreased in the following order: industrial area (IA) > traffic area (TA) > commercial area (CoA) > residential area (RA) > clean area (ClA). Moreover, combined with the analyses conducted using a scanning electron microscope and an energy dispersive X-ray spectrometer (SEM-EDX), it is found that spherical magnetic particles originating mainly from anthropogenic sources were abundant in industrial areas. Baoshan district, which is heavily impacted by industrial activities, showed the highest χ value among the administrative units. Additionally, the correlations of street dust χ value with population, value of industrial output and the gross domestic product (GDP) in Shanghai and other cities indicated that χ is positively correlated with the city GDP as well as the population size (PS) to some extent. This study demonstrates that magnetic parameters of street dust can be used as an effective tool for monitoring environmental pollution and industrial activities in urban environments.

Hexa-mix-chlorinated/brominated benzenes (HXBs), a group of newly found analogues of hexachlorobenzene (HCB) and hexabromobenzene (HBB), may exhibit similar environmental risks and toxicities as HCB and HBB, and therefore possess high interests in environmental and toxicological research. Yet information regarding HXBs in the environment remains scarce. In this study, we developed an isotope dilution method for quantitative and semiquantitative determination of five HXBs in fly ash, soil and air using gas chromatography high resolution mass spectrometry (GC-HRMS) in multiple ion detection mode. The samples were Soxhlet-extracted and purified with multilayer composite silica gel-alumina columns, followed by GC-HRMS detection. Identification of HXBs was conducted by the comparison between theoretical and detected mass spectra using paired-samples T test and cosine similarity analysis. Two HXBs (C₆BrCl₅ and C₆Br₄Cl₂) with reference standards were quantitatively determined while the rest three (C₆Br₂Cl₄, C₆Br₃Cl₃ and C₆Br₅Cl) without reference standards were semiquantitatively analyzed by sharing the calibration curves of C₆BrCl₅ and C₆Br₄Cl₂ in cooperation with isotopologue distribution computation. The accuracies for C₆BrCl₅ and C₆Br₄Cl₂ were 87.3–107.8% with relative standard deviations (RSD) of 2.8–5.0%. The method limits of quantification of the HXBs were 0.10 ng/g in fly ash and soil samples and 0.09 pg/m³ in ambient air samples. The recoveries ranged from 42.7% to 102.1% with RSD of 3.7–13.9%. This method has been successfully applied to the analysis of the HXBs in the environmental samples. The total concentrations of HXBs in the fly ash, soil and ambient air samples were 19.48 ng/g, 10.44 ng/g and 5.13 pg/m³, respectively, which accounted for 10.6%, 0.4% and 10.8% of the corresponding total concentrations of HCB and HBB. This study provides a reference method for quantitative and/or semiquantitative analyses of novel mix-halogenated organic compounds, and sheds light on the full picture of HXBs pollution in the environment.

This review aims to gather and summarize information about the occurrence of emerging contaminants and antibiotic resistance genes in environmental matrices in Latin America. We aim to contribute to future research by compiling a list of priority pollutants adjusted to the needs and characteristics of Latin America, according to the data presented in this study. In order to perform a comprehensive research and secure a representative and unbiased amount of quality data concerning emerging contaminants in Latin America, the research was performed within the Scopus® database in a time frame from 2000 to July 2019. The countries with higher numbers of published articles were Brazil and México, while most studies were performed in the surroundings of Mexico City and in Southern and Southeastern Brazil. The main investigated environmental matrices were drinking water and surface water. The presence of antibiotic resistance was frequently reported, mainly in Brazil. Monitoring efforts should be performed in other countries in Latin America, as well as in other regions of Brazil and México. The suggested priority list for monitoring of emerging contaminants in Latin America covers: di(2-ethylhexyl) phthalate (DEHP), bisphenol-A (BP-A), 4-nonylphenol (4-NP), triclosan (TCS), estrone (E1), estradiol (E2), ethinylestradiol (EE2), tetracycline (TC), amoxicillin (AMOX), norfloxacin (NOR), ampicillin (AMP) and imipenem (IMP). We hope this list serves as a basis for the orientation of the future research and monitoring projects to better understand the distribution and concentration of the listed emerging substances.

Bioaccessibility measurements of polycyclic aromatic hydrocarbons (PAHs) in soils are significant for exposure risk assessment. The current physicochemical methods require tedious operation processes, underestimate the actual risks, or are unsuitable for high organic content soils. In this work, an efficient and convenient method based on polydopamine-coated polyethylene sieve plate (PDA@PESP) and hydroxypropyl-β-cyclodextrin (HPCD) was developed to predict the bioaccessibility of PAHs in multi-type soils. The PDA@PESP can be prepared via in situ self-polymerization, allowing to extract PAHs from HPCD solution quantitatively and rapidly. When applied to evaluate the bioaccessibility with PDA@PESP as an adsorption sink and HPCD as a diffusive carrier, the proposed method can significantly improve the extractable fraction of PAHs compared to single HPCD extraction in particular for high organic carbon content soil and high-ring PAHs. The desorption kinetics data indicated that the method can predict the bioaccessible fraction of PAHs. In addition, the method predicted a satisfactory accumulation into earthworms (Eisenia fetida) with a slope statistically approximated to 1. A highly significant linear regression (R2 = 0.95) was also found between the proposed method and Tenax desorption in historically contaminated soils, demonstrating that the method is an efficient and convenient approach for the bioaccessibility prediction of PAHs in soils.

The performance, microbial community and enzymatic activity of sequencing batch reactors (SBRs) were investigated under 75-day exposure of different Cu(II) concentrations. Cu(II) at 0–5 mg/L had no distinct impact on the chemical oxygen demand (COD) and nitrogen removal, oxygen-uptake rate (OUR), nitrification and denitrification rate, and microbial enzymatic activity. The inhibitory effects of Cu(II) at 10 and 30 mg/L on the nitrogen removal rate, OUR, and microbial enzymatic activity of SBR increased with an increment in operation time due to the Cu(II) biotoxicity and the accumulation of Cu(II) in activated sludge. The changes of microbial reactive oxygen species production, lactate dehydrogenase release, catalase activity and superoxide dismutase activity demonstrated that Cu(II) at 10 and 30 mg/L broke the equilibrium between the oxidation and antioxidation processes in microbial cells and also damaged the cytomembrance integrity, which could affect the COD and nitrogen removal performance and change normal microbial cell morphology. The Cu(II) in the influent could be removed by the microbial absorption and accumulated in the activated sludge under long-term exposure. The microbial community displayed some distinct changes from 0 to 30 mg/L Cu(II). In contrast with 0 mg/L Cu(II), Nitrosomonas, Nitrospira and some denitrifying bacteria obviously decreased in relative abundance under long-term exposure of 10 and 30 mg/L Cu(II).

In recent decades, most lakes in Eastern China have suffered unprecedented nitrogen pollution, making them potential “hotspots” for N2O production and emission. Understanding the mechanisms of N2O production and quantifying emissions in these lakes is essential for assessing regional and global N2O budgets and for mitigating N2O emissions. Here, we measure isotopic compositions (δ15N-N2O and δ18O-N2O) and site preference (SP) of dissolved N2O in an attempt to differentiate the relative contribution of N2O production processes in the shallow, eutrophic Chaohu Lake, Eastern China. Our results show that the bulk isotope ratios for δ15N-N2O, δ18O-N2O, and SP were 5.8 ± 3.9‰, 29.3 ± 13.4‰, and 18.6 ± 3.2‰, respectively. More than 76.8% of the dissolved N2O was produced via microbial processes. Findings suggest that dissolved N2O is primarily produced via nitrification (between 27.3% and 48.0%) and denitrification (between 31.9% and 49.5%). In addition, isotopic data exhibit significant N2O consumption during denitrification. We estimate the average N2O emission rate (27.5 ± 26.0 μg N m−2 h−1), which is higher than that from rivers in the Changjiang River network (CRN). We scaled-up the regional N2O emission (from 1.98 Gg N yr−1 to 4.58 Gg N yr−1) using a N2O emission factor (0.51 ± 0.63%) for shallow lakes in the middle and lower region of the CRN. We suggest that beneficial circumstances for promoting complete denitrification may be helpful for reducing N2O production and emissions in fresh surface waters.

Twenty-six polycyclic aromatic hydrocarbons (PAHs) and four synthetic musk compounds (SMCs) accumulated by Masson pine needles from different areas of Shanghai were investigated in the present study. Concentrations of Σ26PAHs (sum of 26 PAHs) ranged from 234 × 10−3 to 5370 × 10−3 mg kg−1. Levels of Σ26PAHs in different sampling areas followed the order: urban areas (Puxi and Pudong) > suburbs > Chongming. Total concentrations of 16 USEPA priority PAHs ranged from 225 × 10−3 to 5180 × 10−3 mg kg−1, ranking at a relatively high level compared to other regions around the world. Factor analysis and multi-linear regression model has identified six sources of PAHs with relative contributions of 15.1% for F1 (vehicle emissions), 47.8% for F2 (natural gas and biomass combustion), 7.8% for F3 (oil), 10.6% for F4 (coal combustion), 15.7% for F5 (“anthracene” source) and 3.0% for F6 (coke tar). Total concentrations of 4 SMCs varied between 0.071 × 10−3 and 2.72 × 10−3 mg kg−1 in pine needles from Shanghai. SMCs with the highest detected frequency were Galaxolide and musk xylene, followed by musk ketone and Tonalide. The highest level of SMCs was found near industrial park and daily chemical plant. The results obtained from this study may have important reference value for local government in the control of atmospheric organic pollution.

The salinization of freshwater environments is a global concern, and one of the largest sources of salinated water is the mining industry. An increasing number of modern mines are working with low grade sulfide ores, resulting in increased volumes of potentially harmful saline drainage. We used water monitoring data, together with data on sedimentary fossil remains (cladoceran, diatom and chironomid), to analyze the spatio-temporal (5 sampling locations and 3 sediment depths) impact of salinated mine water originating from the Talvivaara/Terrafame open cast mine on multiple components of the aquatic ecosystem of Lake Jormasjärvi, Finland. Lake Jormasjärvi is the fourth and largest lake in a chain of lakes along the path of the mine water. Despite the location and large water volume, the mine water has changed the chemistry of Lake Jormasjärvi, reflected in increased electrical conductivity values since 2010. The ecological impact is significant around the inflow region of the lake, as all biological indicator groups show a rapid and directional shift towards new species composition. There is a clear trend in improved water quality as one moves further from the point of inflow, and as one looks back in time. Our results show that salinated mine water may induce rapid and large scale changes, even far downstream along a chain of several sinking basins. This is of special importance in cases where large amounts of waste water are processed in the vicinity of protected habitats.