Cadmium (Cd) pollution is currently the most serious type of heavy metal pollution throughout the world. Previous studies have shown that Cd elevates the mortality of paddy field spiders, but the lethal mechanism remains to be explored profoundly. In the present study, we measured the activities of protective enzymes (acetylcholinesterase, glutathione peroxidase, phenol oxidase) and a heavy metal chelating protein (metallothionein) in the pond wolf spider Pardosa pseudoannulata after Cd exposure. The results indicated that Cd initially increased the enzyme activities and protein concentration of the spider after 10- and 20-day exposure before inhibiting them at 30-day exposure. Further analysis showed that the enzyme activities in the cephalothorax were inhibited to some extent. Since the cephalothorax region contains important venom glands, we performed transcriptome sequencing (RNA-seq) analysis of the venom glands collected from the spiders after long-term Cd exposure. RNA-seq yielded a total of 2826 differentially expressed genes (DEGs), and most of the DEGs were annotated into the process of protein synthesis, processing and degradation. Furthermore, a mass of genes involved in protein recognition and endoplasmic reticulum (ER) -associated protein degradation were down-regulated. The reduction of protease activities supports the view that protein synthesis and degradation in organelles and cytoplasm were dramatically inhibited. Collectively, our outcomes illustrate that Cd poses adverse effects on the expression of protective enzymes and protein, which potentially down-regulates the immune function in the venom glands of the spiders via the alteration of protein processing and degradation in the ER.

We investigated the in vitro effects of pyriproxyfen on ionic balance in the testis of the zebrafish by measuring ⁴⁵Ca²⁺ influx. In vivo pyriproxyfen treatment was carried out to study oxidative stress, and conduct morphological analysis of the testis and liver. Whole testes were incubated in vitro with/without pyriproxyfen (10⁻¹², 10⁻⁹ or 10⁻⁶ M; 30 min) and ⁴⁵Ca²⁺ influx determined. To study pyriproxyfen’s mechanism of action, inhibitors/activators of ionic channels or pumps/exchangers, protein kinase inhibitors or a calcium chelator were added 15 min before the addition of ⁴⁵Ca²⁺ and pyriproxyfen. We evaluated the in vivo effects of 7 day exposure to waterborne pyriproxyfen (10⁻⁹ M) on reactive oxygen species (ROS) formation, lipid peroxidation, and reduced glutathione content (GSH), glutathione S-transferase (GST), superoxide dismutase (SOD), catalase (CAT) and γ-glutamyltransferase (GGT) activity. Morphological analyses of the testis and liver were carried out after in vivo exposure of D. rerio to pyriproxyfen. Pyriproxyfen increased ⁴⁵Ca²⁺ influx by opening the voltage-dependent T-type channels (T-type VDCC), inhibiting sarco/endoplasmic reticulum ⁴⁵Ca²⁺-ATPase (SERCA) and the NCX exchanger (forward mode) and by mobilizing calcium from stores. The involvement of potassium channels and protein kinase C (PKC) was also demonstrated in pyriproxyfen-induced intracellular calcium elevation. In vivo pyriproxyfen treatment of D. rerio increased lipid peroxidation, decreased GSH content and increased GST activity in testes, in addition to increasing the number and size of spermatogonia cysts and inducing hepatocyte basophilia and dilation of blood vessels in the liver. The toxicity of pyriproxyfen is mediated by calcium overload, increased lipid peroxidation, and a diminished antioxidant capacity in the testis, due to GSH depletion, and altered spermatogenesis. The development of high basophilia in the liver suggests that pyriproxyfen may have estrogenic activity, possibly acting as an endocrine-disruptor. These findings indicate that these alterations may contribute to pyriproxyfen toxicity and spermatogenesis disruption.

Oil spills are a serious environmental problem. To better support risk assessment and pollution control for oil spills, a good understanding of oil transport in the environment is required. This study focused on the numerical simulation of the nearshore oil behaviors based on computational fluid dynamics. Based on the Navier-Stokes momentum equations for an incompressible viscous fluid and volume of fluid (VOF) method, a 3D numerical model of three-phase transient flow was developed. The wave number, averaged flow velocity and oil properties would affect the oil spread extent and the oil volume fraction. The higher the averaged flow velocity and wave number, the lower the oil concentration, and the faster the horizontal movement of the oil. The spilled oil may move to contact the seafloor by increasing the averaged flow velocity at the inlet boundary. Through increasing the wave number, the oil would stay near the water surface. In the nearshore, where the wave is the main seawater motion, the oil containment boom should be set preferentially to the direction of wave transmission for oil cleaning. This study shows that by doubling the wave number and increasing the averaged flow velocity (ten times) at the same time, the maximum oil volume fraction would be reduced by around 32%. Finally, the water temperature had no significant impact on the oil migration, and the impact of evaporation should be considered in the simulation.

Plastic pollution is an emerging problem and is a consequence of the post-consumer plastic waste accumulation in the environment coupled to mismanaged waste programmes. Countries are counteracting the continuous growth of plastic litter with different strategies: introducing bans and limits on both plastic items and materials, promoting plastic recycling and recovery strategies and encouraging voluntary clean up actions, as well as raising public awareness. However, the toxicity of plastics to the environment and organisms is not only related to their polymer chains, but also to the fact that plastic materials contain hazardous additives and can adsorb environmental pollutants (i.e. heavy metals and persistent organic contaminants, respectively). The plastic/additives/pollutants combination may be ingested by marine organisms and then enter in the food chain. Therefore, legislation for additives and contaminants is crucial both to reduce environmental pollution and their toxic effects on organisms, which of course includes humans. In this review, the current policies on plastics and related contaminants are described focusing on current laws. Moreover, recommendations for seafood consumption are suggested, since each fish or mollusc eaten may potentially result in plastic particles, additives or contaminants ingestion.

Groundwater contamination originating from anthropogenic industrial activities is a global concern, adversely impacting health of living organisms and affecting natural ecosystems. Monitoring contamination in a complex groundwater system is often limited by sparse data and poor hydrogeological delineation, so that numerous indicators (organic, inorganic, isotopic) are frequently used simultaneously to reduce uncertainty. We suggest that selected Technology-Critical Elements (TCEs), which are usually found in very low concentrations in the groundwater environment, might serve as contamination indicators that can be monitored through aquifer systems. Here, we demonstrate the use of selected TCEs (in particular, Y, Rh, Tl, Ga, and Ge) as indicators for monitoring anthropogenic groundwater contamination in two different groundwater systems, near the Dead Sea, Israel. Using these TCEs, we show that the sources of local groundwater contamination are phosphogypsum ponds located adjacent to fertilizer plants in two industrial areas. In addition, we monitored the spatial distribution of the contaminant plume to determine the extent of well and spring contamination in the region. Results show significant contamination of the groundwater beneath both fertilizer plants, leading to contamination of a series of wells and two natural springs. The water in these springs contains elevated concentrations of toxic metals; U and Tl levels, among others, are above the maximum concentration limits for drinking water.

Pollution-tolerant lichens are recognized ecological indicators of air pollution in cities, which can also collect airborne anthropogenic particles in their tissues. Harmful (sub)micron-sized magnetites are a ubiquitous component of air particle pollution, adversely impacting human health. In this work, in situ magnetic susceptibility κᵢₛ of well-characterized ultrafine magnetite and lichen thalli were measured to quantify the amount of airborne magnetic particles (AMP) after calibration and to assess the lichen's decontamination over time. Up to 2850 magnetic measurements were carried out in twenty-nine transplanted lichens (collected in urban and clean areas) from winter 2020 to winter 2021. Before the transplants, their initial κᵢₛ values were 0.23–9.45 × 10⁻⁵ SI, representing AMP contents of 0.1–4.6 mg in lichen thalli. After lichens were transplanted to a shared site, the magnetic signals evidenced short-term increases and long-term decreases. After three, five and nine months, the AMP loss is more pronounced for transplanted lichens from polluted (e.g., AMP_5-months loss = 0.59 mg) than clean (= 0.08 mg) sites. Rainfall influenced the lichen's decontamination between seasons. In situ measurements and lichens offer a valued and time-saving methodology for biomonitoring harmful airborne particles simply and effectively.

Despite a growing focus on anthropogenic toxic metal pollution in urban environments, few studies have addressed the problem of quantification when more than two pollution sources are likely present, particularly within complex urban settings in the United States (U.S.). In this study, we utilize the MixSIAR package in R for source apportionment based on Pb isotopic signatures in lichen and road sediment in two urban-industrial centers in SW Ohio (OH). We show that ranges of pollutant contributions are more useful than only visualizing mean or raw values of source apportionment, because this avoids overinterpretation of data when certain sources have a large range of uncertainty. We point out both the dominance of industrial pollution as well as the legacy of leaded gasoline pollution in typical mid-sized U.S. cities, which is evident in both road sediment and lichens. Leaded gasoline contribution to Pb in Middletown, OH lichens mostly vary between ~10 and 25%, while in Hamilton, OH the contribution to lichens and road sediment tends to be relatively negligible except for two road sediment samples and one lichen sample, where median contributions are ~20–30%. Industrial combustion pollution source contributions vary between ~25 and 75% in Hamilton, and ~50–100% in Middletown, OH. Furthermore, comparing pollution sources in lichens to modern particulate matter can provide a record of how pollutant sources change over time, such as our traffic lichen (Sample Li-9) plotting closer to leaded gasoline on a bivariate mixing diagram than modern traffic particulate matter, or our coke plant lichen containing slightly less Pb contribution from industrial combustion sources relative to modern coke plant particulate matter. Lastly, when applicable, multi-source mixing models should be complimented in future studies with additional isotopic source tracers such as Cu, Zn, Nd, and Os to further elucidate unique sources of metal pollutants in addition to Pb.

Black carbon (BC) measurements were performed at Pudong (PD) urban supersite and Gonghexin (GH) roadside station from December 1, 2017 to August 10, 2020 to investigate the variations, source characteristics, and population exposure levels of BC in traffic and urban areas in Shanghai, China. The BC median concentration at GH was more than two-fold that at PD. Absorption Ångström exponent (AAE) values were 1.27 ± 0.17 and 1.31 ± 0.17 at PD and GH, respectively, suggesting the dominance of liquid fossil fuel combustion sources (i.e., traffic exhaust) at these stations. The higher BC and AAE values in winter at PD indicated the relatively increasing contribution of solid fuels (i.e., biomass burning) to BC concentration in urban Shanghai. The diurnal variation in BC showed similar twin-peak patterns at PD and GH, implying that traffic emission mainly contributed to ambient BC concentration in urban Shanghai. The estimated daily intakes (EDIs) of BC were generally higher in males than in females at both PD and GH. The highest BC EDIs at PD were found in age subgroups 1–<2 and 2–<3 years. In contrast, the BC EDIs at GH were observed in age subgroups 6–<9, 12–<15, and 15–<18 years, which were higher than those determined at PD, indicating that more attention must be paid to BC exposure of the population in these age subgroups. These results provide scientific insights into variations, source characteristics, and population exposure levels of BC in urban and traffic areas and could help in the development of BC control strategies in Shanghai.

The current study presents the oxidative potential (OP) along with a wide range of chemical speciation of particulate matter with an aerodynamic diameter less than 10 μm (PM₁₀) at five sites representing different environments in Ahmedabad, a big city in western India. On an average, PM₁₀ concentrations were 116 ± 36, 228 ± 43, 133 ± 29, 101 ± 21, and 70 ± 20 μg m⁻³; volume-normalized OP (OPV) were 2.51 ± 0.71, 5.62 ± 0.68, 2.69 ± 0.76, 2.14 ± 0.41, and 1.55 ± 0.51 nmol DTT min⁻¹ m⁻³; and mass-normalized OP (OPM) were 22 ± 3, 25 ± 5, 21 ± 6, 21 ± 2, and 22 ± 3 pmol DTT min⁻¹ μg⁻¹ over Bapunagar (backward residential area), Narol (industrial), Paldi (bus transport hub), Income Tax (huge running traffic) and Science City (posh residential area), respectively. Overall, OPV showed a significant linear correlation with PM₁₀, whereas OPM showed near uniformity with increasing PM₁₀. Although the OPM values were similar, the site-to-site variability in PM₁₀ concentration reflects the corresponding health risks associated with PM₁₀ exposure for the people living in these areas. Further, a noticeable temporal variation in OPM at Narol and Paldi suggests that species with diverse OPM contributed to PM₁₀ on different days. A strong linear relationship between the ratio of OPV to the mass concentration of organic carbon (OPOC) and the ratio of m/z 43 signal to total water-soluble organic aerosols (WSOA) signals (f43) suggests that the fossil-fuel combustion derived WSOA have higher OP. Furthermore, the relationships of OP with water-soluble trace metals and brown carbon are also investigated and discussed in this paper. Nitrogenous organic compounds particularly emitted from the traffic-related sources in Paldi and Income Tax have higher OPOC than those emitted from other sources over Bapunagar, Narol, and Science City.

The source for Lead (Pb) pollution in soils from the heavily industrialized area located along the coast of the Eastern Mediterranean, Haifa Bay, Northern Israel, is studied using the lead isotopic composition. The uniqueness of the studied data set is that it includes samples of soils, road-wash, and storm-dust sampled for nearly three decades (1988–2017). Road-wash sediments are similar in both elemental and Pb isotopic composition to soils sampled in the same year (2010), indicating re-suspension of local soil, as its origin. Soils sampled during and before 1993 show no evidence for Pb contamination (bulk soil values), although Pb as an additive was already in use. Furthermore, soil overturns hinder the possibility to trace changes in the Pb isotopic composition with time in soils of the same location. Soils sampled from 1995–8 to 2013 were significantly dominated by Post-1992 Pb additive, pointing to Pb’s peak as an additive. Soils Pb and Zn Enrichment factors for most samples are below 5, and their anthropogenic source is likely common. Forest fire enriched Pb and Zn in the soil, and their Pb isotope compositions reflect this enrichment. Lead from the Hod Assaf recycling plant detected up to some 2.5 km away, and although not analyzed in the current study, dioxin-like compounds possibly accompanied Pb.