Total concentration and chemical partitioning of heavy metals are commonly used in environmental quality assessment; however, their comparability and comprehensive application are far less discussed. Herein, bioavailability, pollution and eco-risk of As, Cd, Cr, Cu, Ni, Pb and Zn in surface sediments of Erhai Lake were evaluated referring to multiple indices following the experimental methods of complete digestion, optimized Community Bureau of Reference (BCR) and 1.0 M HCl extractions. Results of bioavailability for most metals were similar and comparable from BCR and HCl extractions. While bioavailable concentrations of Cd and Pb from HCl extraction were significantly (p < 0.01) lower than those from BCR extraction, indicating BCR extraction is more efficient. Results of enrichment factor (EF) and concentration enrichment ratio (CER) suggested that Cd was the highest polluted element followed by As, Pb and Zn, whereas Cr, Cu and Ni were mainly natural in origin. Similar concentrations of anthropogenic As from EF and CER assessments indicated anthropogenic As mainly existed in bioavailable form. However, anthropogenic Cd, Pb and Zn existed in both bioavailable and residue forms, resulting in the underestimation of anthropogenic metals by the CER assessment. The sediment quality guidelines (SQGs), potential ecological risk index (Er) and risk assessment code (RAC) showed inconsistent eco-risks for each of the metals except Cd. Combining pollution level and chemical partitioning with SQGs, Er and RAC assessments, high eco-risk of Cd, moderate eco-risk of As and Pb, and low eco-risk of Cr, Cu, Ni and Zn were graded. Our study highlights the limitation of single index and the necessity of integrating multiple indices following total concentration and chemical partitioning in metal pollution and eco-risk assessments.

In the past decades, research on water pollution microplastics (MPs) has intensified tremendously. However, the relationship between MPs and environmental factors in urban river networks is under researched. Our study selected 65 sampling sites from a sophisticated urban river network system in Shanghai Municipality, China. Here, the combined influence of land-use types, river width, and water quality parameters to explore MPs distribution patterns. We found that MPs abundance ranged from 0.7 to 24.3 items/L, and the spatial difference in abundance was significant at a limited number of sampling sites. Fibrous MPs were the most abundant MPs in the river system. 72.7% of MPs <3 mm. Of the ten polymers detected, polypropylene and polyethylene terephthalate were predominant. In addition, cotton fiber was the main non-plastic component found in the samples. Moreover, land-use types showed no significant impact on MPs in the buffer zone of the sampling sites. However, point source pollution may cause an abnormal increase in MPs abundance. Through redundant analysis, we found that the phytoplankton abundance (e.g., chlorophyll-a) was influenced by MPs shape, while the river width influence MPs size. Construction activities were identified as the leading point source of pollution for the abnormal increase in local MPs pollution. Our results will inform on MPs distribution patterns in the super-metropolis river system.

In this study, the influencing factors and sources of historical changes in polycyclic aromatic hydrocarbons (PAHs) in the sediment core of Fuxian Lake were analyzed. Before 1970, the Σ₁₆PAH concentration fluctuated widely, with one or more maximum values. During 1971–2004, the Σ₁₆PAH concentration showed a slow growth trend, while during 2005–2017, the concentration increased sharply, reaching a peak value of 821 ng g⁻¹. dw in 2017. The results of a positive matrix factorization (PMF) model demonstrated that before 1970, PAHs were mainly derived from biomass burning in the Fuxian Lake sediment core, with an overall contribution of 40 %. During 1971–2004, the source of PAHs was mainly coal combustion, with an overall contribution of 34 %. During 2005–2017, PAHs primarily originated from traffic, with an overall contribution of 33 %. Population, coal, GDP, motor, and petroleum had a significant influence on low molecular weight (LMW) PAHs in 1980–2004 and 2005–2017. Motor, coal, population, and GDP had a greater impact on high molecular weight (HMW) PAHs. Before 1970 and in 1971–2004, meteorological factors had little effect on PAHs in the sediment core in Fuxian Lake. During 2005–2017, day and rainfall were significantly negatively correlated with HMW PAHs, while temperature and wind were not correlated with PAH concentrations. During 2005–2017, total organic carbon (TOC) and total nitrogen (TN) had greater adsorption effects on HMW PAHs than on LMW PAHs. Before 1970 and in 1971–2004, the adsorption effects of TOC and TN on 3–4-ring PAHs were greater than those of 2-ring and 5–6-ring PAHs. Total phosphorus (TP) had no adsorption effect on PAHs in the entire sedimentary column.

The hazardous effects of herbicides are well known; however, their effects on the reproductive system remain unclear. In this study, we demonstrated the anti-proliferative effects of dinitramine (DN) on immature murine testicular cell lines (Leydig and Sertoli cells) mediated via endoplasmic reticulum (ER) stress-induced calcium dysregulation in the cytosol and mitochondria. The results demonstrated that the viability and proliferation of DN-treated TM3 and TM4 cells decreased significantly, even in the spheroid state. DN induced the apoptosis of TM3 and TM4 cells and decreased the expression of genes related to cell cycle progression. Treatment with DN increased the cytosolic and intramitochondrial levels of calcium by activating ER stress signals. DN activated the Erk/P38/Jnk Mapk pathway and inactivated the Pi3k/Akt pathway in murine testicular cells. Co-treatment with 2-aminoethoxydiphenyl borate (2-APB) mitigated DN-induced calcium upregulation in both testicular cell lines. Although 2-APB did not antagonize the anti-proliferative effect of DN in TM3 cells, treatment with 2-APB and 1,2-bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid restored the proliferation of DN-treated TM4 cells.

The remarkable journey of progression of mankind has created various impacts in the form of polluted environment, amassed heavy metals and depleting resources. This alarming situation demands sustainable energy resources and approaches to deal with these environmental hazards and power deficit. Pyrolysis and co-pyrolysis address both energy and environmental issues caused by civilization and industrialization. The processes use hazardous waste materials including waste tires, plastic and medical waste, and biomass waste such as livestock waste and agricultural waste as feedstock to produce gas, char and pyrolysis oil for energy production. Usage of hazardous materials as pyrolysis and co-pyrolysis feedstock reduces disposal of harmful substances into environment, reducing occurrence of soil and water pollution, and substituting the non-renewable feedstock, fossil fuels. As compared to combustion, pyrolysis and co-pyrolysis have less emission of air pollutants and act as alternative options to landfill disposal and incineration for hazardous materials and biomass waste. Hence, stabilizing heavy metals and solving the energy and waste management problems. This review discusses the pyrolysis and co-pyrolysis of biomass and harmful wastes to strive towards circular economy and eco-friendly, cleaner energy with minimum waste disposal, reducing negative impact on the planet and creating future possibilities.

The extensive use of semiconducting nanoparticles such as quantum dots in biomedical and industrial products can lead to their inadvertent release into the freshwater system. Natural exudates in the aquatic system comprising extracellular polymeric substance (EPS) and protein-rich metabolites can eventually adsorb onto the quantum dots (QDs) surface and form an eco-corona. The alterations in the physio-chemical and toxicological behavior of CdSe/ZnS QDs under the influence of eco-corona in the freshwater system have not been explored yet. In the present study, lake water medium conditioned with exudate secreted by Scenedesmus obliquus was utilized as an eco-corona forming matrix. The time-based evolution of the eco-corona on the differently charged CdSe/ZnS QDs was analyzed using transmission electron microscopy and dynamic light scattering. Aging of amine-QDs in algal exudate for 72 h showed enhanced aggregation (Mean Hydrodynamic Diameter- 1969 nm) as compared to carboxyl-QDs (1543 nm). Further, eco-coronation tends to impart an overall negative charge to the QDs. The fluorescence intensity of amine-QDs was quenched by 84% due to the accumulation of higher eco-corona. An integrative effect of surface charge and accumulated eco-corona layer influenced the Cd²⁺ ion leaching from the QDs. An enhancement in the algal cell viability treated with carboxyl - CdSe/ZnS (90%) and amine- CdSe/ZnS QDs (94%) aged for 72 h suggested that eco-corona can effectively mitigate the inherent toxicity of the QDs. The oxidative stress markers in the algal cells (LPO, SOD, and CAT) were in correlation with the cytotoxicity results. The algal photosynthetic efficiency depended on the deposition of eco-coronated QDs on the cell surface. Cellular uptake results indicated low Cd²⁺ concentration of nearly 13.9 and 11.5% for carboxyl- and amine- CdSe/ZnS QDs respectively. This suggests that eco-coronation directly influences the bioavailability of engineered nanoparticles.

Packaging is necessary for preserving and delivering products and has significant impacts on human health and the environment. Particle matter (PM) may be released from packages and transferred to the air during a typical peeling process, but little is known about this package-to-air migration route of particles. Here, we investigated the emission profiles of total and biological particles, and the horizontal and vertical dispersion abilities and community structure of viable microbes released from packaging to the air by peeling. The results revealed that a lot of inhalable particles and viable microbes were released from package to the air in different migration directions, and this migration can be regulated by several factors including package material, effective peeling area, peeling speed and angles, as well as the characteristics of the migrant itself. Dispersal of package-borne viable microbes provides direct evidence that viable microbes, including pathogens, can survive the aerosolization caused by peeling and be transferred to air over different distances while remaining alive. Based on the experimental data and visual proof in movies, we speculate that nonbiological particles are package fibers fractured and released to air by the external peeling force exerted on the package and that microbe dispersal is attributed to surface-borne microbe suspension by vibration caused by the peeling force. This investigation provides new information that aerosolized particles can deliver package-borne substances and viable microbes from packaging to the ambient environment, motivating further studies to characterize the health effects of such aerosolized particles and the geographic migration of microbes via packaging.

Mejillones Bay is a coastal ecosystem situated in an oxygen-deficient upwelling area impacted by mining activities in the coastal desert region of northern Chile, where conspicuous microbial life develops in the sediments. Herein, heavy metal (loid)s (HMs) such as Cu, Pb, As, Zn, Al, Fe, Cd, Mo, Ni and V as well as benthic microbial communities were studied using spectrometry and iTag-16 S rRNA sequencing. Samples were taken from two contrasting sedimentary localities in the Bay named Punta Rieles (PR) and Punta Chacaya (PC) within 10–50 m water-depth gradient. PR sediments were organic matter rich (21.1% of TOM at 50 m) and overlaid with low-oxygen waters (<0.06 ml O2/L bottom layer) compared with PC. In general, HMs like Al, Ni, Cd, As and Pb tended to increase in concentration with depth in PR, while the opposite pattern was observed in PC. In addition, PR presented a higher number of unique families (72) compared to PC (35). Among the top ten microbial families, Desulfobulbaceae (4.6% vs. 3.2%), Flavobacteriaceae (2.8% vs. 2.3%) and Anaerolineaceae (3.3% vs. 2.3%) dominated in PR, meanwhile Actinomarinales_Unclassified (8.1% vs. 4.2%) and Sandaracinaceae (4.4% vs. 2.0%) were more abundant in PC. Multivariate analyses confirmed that water depth-related variation was a good proxy for oxygen conditions and metal concentrations, explaining the structure of benthic microbial assemblages. Cd, Ni, As and Pb showed uniformly positive associations with communities that represented the keystone taxa in the co-occurrence network, including Anaerolineaceae, Thiotrichaceae, Desulfobulbaceae, Desulfarculaceae and Bacteroidales_unclassified communities. Collectively, these findings provide new insights for establishing the ecological interconnections of benthic microorganisms in response to metal contamination in a coastal upwelling environment.

Butyl Xanthate (BX) is a typical flotation reagent used to extract non-ferrous nickel ores, discharged into the surrounding environment of mining areas in large quantities. However, few studies have focused on the toxicity of combined pollution of BX and nickel (Ni) on aquatic plants, especially phytoplankton, the main producer of aquatic ecosystems. The toxicity and potential mechanism of single and combined pollution of BX and Ni at different concentrations (0–20 mg L⁻¹) on typical freshwater algae (Chlorella pyrenoidosa) were studied. BX slightly stimulated the growth of C. pyrenoidosa on the first day, but Ni and Ni/BX mixture significantly inhibited it during incubation. Results showed that the inhibition rate (I) of the pollutants on the growth of C. pyrenoidosa followed the order: Ni/BX mixture > Ni > BX. The 96-h 20% effective inhibitory concentrations (96h-EC₂₀) of Ni and BX on C. pyrenoidosa growth were 3.86 mg L⁻¹ and 19.25 mg L⁻¹, respectively, indicating C. pyrenoidosa was sensitive to pollutants. The content of total soluble protein (TSP) and chlorophyll a (Chl-a) changed significantly, which may be caused by the damage of pollutants to cell structures (cell membranes and chloroplasts). In addition, the I of pollutants on C. pyrenoidosa growth was related to dose, superoxide dismutase (SOD), catalase (CAT) and malondialdehyde (MDA). The increasement of reactive oxygen species (ROS), antioxidant enzymes (SOD and CAT), and MDA content, suggested C. pyrenoidosa suffered from oxidative stress, leading to lipid oxidation. These results will help to understand the toxicity mechanism of pollutants in typical mining areas and assess the environmental risks of pollutants to primary producers in aquatic ecosystems.

Because most relevant studies have used small sample sizes, to date, representative atmospheric monitoring of persistent organic pollutants (POPs) on a regional scale has been very limited, which makes it difficult to precisely identify “hotspots” and possible pollution sources. In this study, an ultrahigh resolution monitoring technique was used to measure the atmospheric spatial variations in POP concentrations on a regional scale, throughout Campania, Italy. The occurrence of specific POPs—including polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs) and phthalate esters (PAEs)—were investigated using polyurethane foam-based passive air samplers (PUF-PAS), which were deployed at 129 sites across the Campania Territory between April and July 2016. The results show that the highest POP levels occurred in the Naples metropolitan area (NMA), although there were other problematic spots throughout the Territory. More specifically, hotspot areas in the NMA that depict serious POP pollution were found in the Bagnoli brownfield site, Sarno River Basin, and parts of the northeastern NMA sector. The atmospheric POP contamination in Campania is jointly controlled by the contributions of local emissions and long-range atmospheric transport. Diffusion model was employed to identify the potential sources of various POPs. The simulation showed that all the POP sources are located in the NMA and are closely related to industrial sites. This study demonstrates the advantage of using large sample sizes to identify POP source locations and achieve geospatial visualization of POP concentration and risk assessment levels.