Microorganisms are ubiquitous in the atmosphere, where they can disperse for a long distance. However, it remains poorly understood how these airborne microorganisms vary and which factors influence the microbial distribution in different anthropogenic activity regions. To explore the regional differences of bacteria and fungi in airborne particles, PM₂.₅ and PM₁₀ samples were collected in the urban and rural areas of Hangzhou. The bacterial and fungal communities in the urban atmosphere was more similar to each other than those in the rural atmosphere. Analyses conducted by the concentration weighted trajectory model demonstrated that the local environment contributed more to the similarity of airborne bacteria and fungi compared with the atmospheric transport. The concentrations of local air pollutants (PM₂.₅, PM₁₀, NO₂, SO₂ and CO) were positively correlated with the similarity of the bacterial and fungal communities. Additionally, the concentrations of these air pollutants in the urban site were about 1.5 times than those in the rural site. This implicated that anthropogenic activity, which is the essential cause of air pollutants, influenced the similarity of airborne bacteria and fungi in the urban area. This work ascertains the outdoor bacterial and fungal distribution in the urban and the rural atmosphere and provides a prospective model for studying the contributing factors of airborne bacteria and fungi.

A biofilm reactor was designed with flat ceramic substrates to remove Co(II), Ni(II) and Zn(II) from industrial wastewater. The ceramics were made of clay and nano-rubber with high mechanical resistance. The surface of the ceramic substrate was modified with neutral fiber and nano-hydroxyapatite. A uniform and stable biofilm mass of 320 g with 2 mm of thickness was produced on the modified ceramic after 3 d. The micro-organisms were identified in the biofilm by polymerase chain reaction (PCR) method. Functional groups of biofilms were identified with a Fourier transform infrared spectrometer (FT-IR). Experiments were designed by central composite design (CCD) using the responsive surface method (RSM). The biosorption process was optimized at pH = 5.8, temperature = 22 °C, feed flux of heavy metal wastewater = 225 ml, substrate flow = 30 ml, and retention time = 7.825 h. The kinetic data was analyzed by pseudo first-order and pseudo second-order kinetic models. Isotherm models and thermodynamic parameters were applied to describe the biosorption equilibrium data of the metal ions on the biofilm-ceramic. The maximum biosorption efficiency and capacity of heavy metal ions were about 72% and 57.21 mg, respectively.

Terrestrial environments are subject to extensive pollution by plastics and, based on the slow degradation of plastics, are likely to act as long term sinks for microplastic debris. Currently the hazards of microplastics in soil and the potential impacts on soil organisms is poorly understood. Particularly the role of particle characteristics, such a size or polymer type, in dose-response relationships for microplastics is not known. The aim of this study was to assess the ingestion and toxicity of nylon (polyamide) particles, in three different size ranges, to Enchytraeus crypticus in a soil exposure. Effects were also compared with those of polyvinyl chloride (PVC) particles, in a single size range. Nylon particle ingestion was confirmed using fluorescence microscopy, with greatest ingestion for particles in the smallest size range (13–18 μm). To investigate how particle size affected survival and reproduction, E. crypticus were exposed to nylon particles in two well-defined size ranges (13–18 and 90–150 μm) and concentrations of 20, 50, 90 and 120 g/kg (2–12% w/w). An intermediate nylon size range (63–90 μm) and a larger sized PVC particle (106–150 μm), both at 90 g/kg, were also tested. Survival was not affected by either of the polymer types or sizes. Reproduction was significantly reduced, in a dose-dependent manner, by the nylon particles at high exposure concentrations (>90 g/kg). Smaller size ranges (13–18 μm) had a greater effect compared to larger size ranges (>63 μm), with a calculated EC₅₀ for the 13–18 μm size range of 108 ± 8.5 g/kg. This greater hazard could be qualitatively linked with the ingestion of a greater number of smaller particles. This study highlights the potential for toxic effects of plastics in small size ranges to soil organisms at high exposure concentrations, providing understanding of the hazards microplastics may pose in the terrestrial environment.

Persistent organic pollutants (POPs), including Perfluoroalkyl substances (PFASs), enter into the marine ecosystem, raising questions on possible adverse effects caused to the health of marine organisms and especially of top predators. Thus, there is an urge to assess the occurrence and the tissue distribution of PFASs in apex predators. To this end, the current study examines concentrations and distribution of 15 PFASs among 85 samples of different tissues from 9 shark and ray species collected in Greece. The results showed a similar PFAS pattern among the different tissues, with long carbon chain PFASs being the most frequently detected compounds. PFTrDA was the most predominant compound in terms of concentration and frequency of detection, followed by PFUnDA and PFOS. PFTrDA concentrations ranged between < LOQ and 27.1 ng/g ww, while PFUnDA and PFOS levels ranged from <LOQ to 16.0 and < LOQ to 21.6 ng/g ww, respectively. Regarding their frequency of detection, PFTrDA and PFUnDA were detected in 98% and 91% of the samples, respectively, while PFOS was detected in 79%. ΣPFAS concentrations in each analysed tissue ranged from 0.3 to 85 ng/g ww, with the latter being detected in the liver of angular roughshark (Oxynotus centrina). On average, PFASs were found to be accumulated in tissues in the following order: gonads > heart > liver ≈ gills > muscle. Relative contribution (%) of individual compounds to ΣPFAS concentration varied among the different shark tissues, and also among the different shark species. No correlation between PFASs levels in tissues and sharks’ gender, length and geographical origin was observed.

Dibutyl phthalate (DBP), one of the most widely used plasticizers, is a known environmental endocrine disruptor that impairs male and female fertility. In this study, oral administration of DBP was given to pregnant mice on 14.5 days post coitus (dpc) for 3 days; and additionally, DBP was added into the culture of 14.5 dpc fetal ovaries for 3 days. DBP exposure during gestation disturbed the progression of meiotic prophase I of mouse oocytes, specifically from the zygotene to pachytene stages. Meanwhile, the DBP-exposed pachytene oocytes showed increased homologous recombination sites and unrepaired DNA damage. Furthermore, DBP caused DNA damage by increasing oxidative stress, decreased the expression of multiple critical meiotic regulators, and consequently induced oocyte apoptosis. Moreover, the effect of DBP on meiosis I prophase involved estrogen receptors α and β. Collectively, these results demonstrated a set of meiotic defects in DBP-exposed fetal oocytes. As aberrations in homologous recombination can result in aneuploid gametes and embryos, this study provides new support for the deleterious effects of phthalates.

Photocatalytic degradation is an attractive strategy to purify waste water contaminated by macromolecular organics. Compared with the single-component photocatalysts, heterostructures of different semiconductors have been widely used to improve the photocatalytic performance. In this work, we fabricate a hetero-structured photocatalyst consisting of two-dimensional graphitic carbon nitride (g-C3N4) nanosheets and commercial MoO3 microparticles through a simple mixing and annealing process. The photocatalytic performance was evaluated in various dye degradation reactions, especially Rhodamine (RhB) degradation. The MoO3/g-C3N4 composite shown a significant improvement compared with individual MoO3 or g-C3N4 as well as their physical mixture. By applying electron spin resonance (ESR) spin-trap spectra, radical scavenge experiments and electrochemical analysis, we find that a direct Z-scheme charge transfer between MoO3 and g-C3N4 not only causes an accumulation of electrons in g-C3N4 and holes in MoO3, but also boosts the formation of superoxide radical and hydroxyl radical. The superoxide radical and hole dominate the photocatalytic degradation, while the hydroxyl radical plays a negligible role and its production can be suppressed by lowering the pH value.

Iron-bearing clays are ubiquitously distributed as mineral dusts in the atmosphere. Bromophenols were reported as the major products from thermal decomposition of the widely used brominated flame retardants (BFRs). However, little information is available for the reactivity of iron associated with mineral dusts to interact with the atmospheric bromophenols and the subsequent toxic effects. Herein, three common clay minerals (montmorillonite, illite and kaolinite) were used to simulate mineral dusts, and the reactions with gaseous 2-bromophenol were systematically investigated under environmentally relevant atmospheric conditions. Our results demonstrate that structural Fe(III) in montmorillonite and Fe(III) from iron oxide in illite mediated the dimerization of 2-bromophenol to form hydroxylated polybrominated biphenyl and hydroxylated polybrominated diphenyl ether. The surface reaction is favored to occur at moisture environment, since water molecules formed complex with 2-bromophenol and the reaction intermediates via hydrogen bond to significantly lower the reaction energy and promote the dimerization reaction. More importantly, the formed dioxin-like products on clay mineral dust increased the toxicity of the particles to A549 lung cell by decreasing cell survival and damaging cellular membrane and proteins. The results of this study indicate that not only mineral dust itself but also the associated surface reaction should be fully considered to accurately evaluate the toxic effect of mineral dust on human health.

The below-cloud washout (BCW) effect on PM₂.₅ concentration during periods of rain is still a subject of debate. Existing BCW schemes for PM₂.₅ have large deficiencies that influence its simulation in 3D chemical transport models (CTMs). In this study, a 7-year dataset with high temporal resolution (in minutes) sampled from a pristine rural site is used to calculate the BCW coefficient during the rain events. The data used for the BCW coefficient calculation cover a wide range of rain intensity from 2 mm h⁻¹ to 60 mm h⁻¹. The BCW coefficient linearly correlates with the rain intensity, with a correlation coefficient of 0.82. The coefficient has a magnitude of 10⁻⁵ to 10⁻⁴ s⁻¹ when the rain intensity ranges from 1 to 40 mm h⁻¹. After implementing the updated BCW scheme into the Comprehensive Air Quality Model with Extensions (CAMx) model, the performance of PM₂.₅ simulation improves for the two months of heavy rain. Apart from the CAMx model, our scheme can be easily implemented into other 3D CTMs to improve PM₂.₅ simulation during rainy days. The BCW effect can clean around 10–40% of the PM₂.₅ over our study region, which can help to reduce the PM₂.₅ exposure level for residents, and the health burdens caused by this pollutant can thus be reduced. Rainmaking is a potential way to decrease PM₂.₅ concentration, but it cannot be the key method to reduce the PM₂.₅ level to the standard during episodic cases (e.g., >200 μg/m³).

Bioelectrochemical systems (BESs) have been widely investigated for recalcitrant waste treatment mainly because of their waste removal effectiveness. Electroactive microbes (EMs) have long been thought to contribute to the high effectiveness by interacting with electrodes via electron chains. However, this work demonstrated the dispensable role of EMs for enhanced recalcitrant contamination degradation in BESs. We revealed enhanced p-fluoronitrobenzene (p-FNB) degradation in a BES by observing a defluorination efficiency that was three times higher than that in biodegradation or electrochemical processes. Such an improvement was achieved by the collaborative roles of electrode biofilms and planktonic microbes, as their individual contributions to p-FNB degradation were found to be similarly stimulated by electricity. However, no bioelectrochemical activity was found in either the electrode biofilms or the planktonic microbes during stimulated p-FNB degradation; because no biocatalytically reductive or oxidative turnovers were observed on cyclic voltammetry curves. The non-involvement of EMs was further proven by the similar microbial community evolution for biofilms and planktonic microbes. In summary, we proposed a mechanism for indirect electrical stimulation of microbial metabolism by electrochemically generating the active mediator p-fluoroaniline (p-FA) and further degradation by a sequential combination of electrochemical p-FNB reduction and biological p-FA oxidation by non-EMs.

Inspired by methods used for life cycle impact assessment (LCIA), we constructed a series of indicators to appreciate the noxiousness of radioactive materials and wastes for human and ecosystem health. According to known potential human health and ecological effects of such materials, six main impact categories were considered to initiate the development of the method: human cancer and non-cancer effects vs. ecotoxicity, considering both chemotoxicity and radiotoxicity. For ecosystems, the noxiousness indicator is based on the concept of Potentially Affected Fraction (PAF), used as a damage indicator at the ecosystem level. The PAF express the toxic pressure on the environment due to one substance. It has been enlarged to mixtures of substances as multi-substances PAF (ms-PAF), and applied to a mix of stable and radioactive substances. Combining ecotoxicity data and a simplified model of exposure of fauna and flora, we proposed a chemotoxicity indicator and a radiotoxicity indicator, ultimately aggregated into a single indicator simply by addition.According to acknowledged practices in LCIA and corresponding available data, we suggested implementing to human health an approach similar to that applied to ecosystems. We produced eigth basic indicators combining effects categories (cancer and non cancer), exposure pathways (ingestion and inhlation) and substances (chemicals and radionuclides). The principle of additivity supporting the whole proposed approach allows their complete aggregation into a single indicator also for human health. Different source terms may be then easily directly compared in terms of human and ecological noxiousness.Applied to the time evolution of a High Level radioactive Waste (HLW), the method confirmed over 1 million years the dominance of the radiotoxicity in the noxiousness of the material for both humans and environment. However there is a change with time in the ranking of the most noxious substances, with stable metals contribution going progressively up. Finally, the HLW global noxiousness, integrating human health and ecological aspects, was assessed through time at three stages and showed a temporal decrease as expected from the dominance of the radiotoxicity.