Brown carbon (BrC) has been proposed as an important driving factor in climate change due to its light absorption properties. However, our understanding of BrC’s chemical and optical properties are inadequate, particularly at remote regions. This study conducts a comprehensive investigation of BrC aerosols in summer (Aug. 2013) and winter (Jan. 2014) at Southeast Tibetan Plateau, which is ecologically fragile and sensitive to global warming. The concentrations of methanol-soluble BrC (MeS-BrC) are approximately twice of water-soluble BrC (WS-BrC), demonstrating the environmental importance of water-insoluble BrC are previously underestimated with only WS-BrC considered. The mass absorption efficiency of WS-BrC (0.27–0.86 m² g⁻¹) is lower than those in heavily polluted South Asia, indicating a distinct contrast between the two sides of Himalayas. Fluorescence reveals that the absorption of BrC is mainly attributed to humic-like and protein-like substances, which broaden the current knowledge of BrC’s chromophores. Combining organic tracer, satellite MODIS data and air-mass backward trajectory analysis, this study finds BrC is mainly derived from bioaerosols and secondary formation in summer, while long-range transport of biomass burning emissions in winter. Our study provides new insights into the optical and chemical properties of BrC, which may have implications for environmental effect and sources of organic aerosols.

The traditional assessment of agricultural soil remediation technologies pay limited attention to sustainability and only considers the decrease in contaminant concentrations and cost, even though the sustainability of these technologies has been prioritized. This 3-year field study comprehensively assessed the sustainability of four commonly used agricultural soil remediation technologies in terms of metal(loid) removal efficiency, environmental merit, and cost. The farmland was contaminated by previous sewage irrigation with excessive amounts of As, Cd, and Pb. The four selected remediation technologies used were phytoextraction, intercropping of hyperaccumulators and cash crops, chemical immobilization, and turnover and attenuation (T&A). A risk reduction–environmental merit–cost model was utilized to compare these four technologies. Results showed that T&A reduced the health risks posed by excess metal(loid)s by ∼47% and yielded the highest risk reduction and lowest cost. Phytoextraction achieved the highest environmental merit because it produced the least interruption to the environment. A simplified assessment frame for soil remediation technology was established from a retrospective aspect using data from a real soil remediation project. Environmental merit is a less considered factor and more difficult to quantify than risk reduction or cost, thus requiring increased attention.

Cadmium (Cd) contamination is a big challenge for managing food supply and safety around the world. Reduction of the bioaccumulation of cadmium (Cd) in wheat is an important way to minimize Cd hazards to human health. This study compared and highlighted the effects of soil and foliar applications of Zn on Cd accumulation and toxicity in cultivars with high Cd accumulation (high-Cd wheat) and low Cd accumulation (low-Cd wheat). Both foliar and soil Zn applications provided effective strategies for reducing wheat grain Cd concentrations in the high-Cd wheat by 26–49% and 25–52%, respectively, and these also significantly reduced the concentrations in wheat stems and leaves. Foliar and soil Zn applications significantly reduced Cd in leaves and stems of the low-Cd wheat but had no effects on grain Cd. Both soil and foliar Zn applications significantly alleviated Cd toxicity by regulation of Cd transport genes, as reflected by the increased grain yield and antioxidant enzyme activity in the wheat tissues. Gene expression in response to zinc application differed in the two wheat cultivars. Down-regulation of the influx transporter (TaNramp5) and upregulation of the efflux transporters (TaTM20 and TaHMA3) in the high-Cd wheat may have contributed to the Zn-dependent Cd alleviation and enhanced its tolerance to Cd toxicity. Additionally, foliar Zn applications down-regulated the leaf TaHMA2 expression that reduced root Cd translocation to shoots, while soil Zn applications down-regulated the root TaLCT1 expression, which contributed to the reduction of root Cd concentrations. Soil (99 kg ZnSO₄·7H₂O ha⁻¹) and foliar (0.36 kg ZnSO₄·7H₂O ha⁻¹) Zn applications can effectively decrease the Cd in grains and guarantee food safety and yield, simultaneously. The presented results provide a new insight into the mechanisms of, and strategies for, using Zn for the Cd reduction in wheat.

Tea plants (Camellia sinensis (L.) O. Kuntze) can hyperaccumulate fluoride (F). The accumulation of F in tea leaves may induce serious health problems in tea consumers. It has been reported that selenium (Se) could reduce the accumulation of heavy metals in plants. Thus, the aim of this study was to investigate whether exogenous Se could reduce F accumulation in tea plant. The results showed that Se treatment could decrease F content in tea leaves, increase F accumulation in roots, decrease the proportion of water-soluble F in tea leaves and increase the Se content. Low F levels promoted the accumulation of Se in tea plants. Se treatment could modulate F-induced oxidative injury by decreasing malondialdehyde level and increasing the activities of superoxide dismutase, peroxidase and catalase. Moreover, Se inhibited F-induced increase in leaf iron, calcium, aluminum, leaf and root magnesium and lead contents. These results showed that Se application could decrease F content and increase Se content in tea leaves, which may be served as a novel strategy for production of healthy tea.

Given that studies on actual sewage treatment plants are often affected by environmental conditions, it is challenging to clearly understand the associated bioaerosol generation and diffusion characteristics during the aeration process. Therefore, to enhance understanding in this regard, in this study, bioaerosol generator was used to simulate bioaerosol generation and diffusion under two aeration modes, i.e., bubble bottom aeration and brush surface aeration. The total concentration range of culturable bacteria in the bioaerosol produced by bubble bottom aeration and that produced by brush surface aeration were 300–3000 CFU/m³. Under bubble bottom aeration, the generated bioaerosol was symmetrically distributed around the source point, whereas under brush surface aeration, it was primarily distributed in the forward direction of the rotating brush surface. These bioaerosols from bubble bottom aeration predominantly consisted of particles with sizes below 3.3 μm, particularly those with sizes in the range 1.1–2.1 μm. On the contrary, the bioaerosols produced via brush surface aeration predominantly consisted of particles with sizes above 3.3 μm. The distribution characteristics of population structure in the two aeration modes were consistent with the distribution characteristics of concentration in the corresponding models. Additionally, the results showed that when the aeration process is unaffected by environmental conditions (particle matters, wind direct, wind speed, etc.), the bioaerosol components originate primarily from the parent sewage or sludge, and do not diffuse far from the source point. Therefore, source reduction (capping or sealing) can be recommended as the primary control strategy for bioaerosols in sewage treatment plants. The adoption of such measures will significantly limit the diffusion of bioaerosols, thereby reducing the potential risks associated with human exposure.

In China, excessive phosphorus (P) application in protected vegetable fields has led to high legacy P stores. Soil amendment with alum or dolomite is one of many best management practices (BMPs) used to reduce P losses in calcareous soils. However, both the kinetics and mechanisms of P sorption and soil available P in amended soils are understudied. Herein, both aspects were looked at under controlled conditions. Firstly, a sorption study which coupled P concentrations with poorly-crystalline Al hydroxides and dolomite was conducted. Results from this batch experiment showed that P sorption on poorly-crystalline Al hydroxides was homogenous and occurred mainly via displacement of inner-sphere hydroxyl (Al–OH) instead of the formation of AlPO₄. However, the amount of sorbed P reached maximum sorption of 73.1 mg g⁻¹ and did not change with further increase in P concentration. It was observed that P adsorbed onto the dolomite surface at low P concentrations, whereas hydroxyl replacement and uneven cluster precipitation of Ca₃(PO₄)₂ occurred at high P concentrations. A second 90 day incubation experiment investigated changes to soil available P and sorption-desorption across variable rates of amendments (0–50 g kg⁻¹). Results showed that alum amendment at a rate of 50 g kg⁻¹ decreased soil CaCl₂–P and Olsen-P concentrations by 91.9% and 57.8%, respectively. However, Olsen-P increased when the dolomite rates were <20 g kg⁻¹. Phosphorus sorption-desorption of the amended soil showed alum had higher P sorption efficiency than dolomite at low addition rates (<10 g kg⁻¹). However, soil amended with high dolomite rates (>10 g kg⁻¹) could sorb more P in comparison with alum when P concentrations were increased. The P status of the amended soil was closely connected to the P sorption mechanisms on mineral amendments, soil P concentrations and soil properties.

Plant-derived materials as environmentally friendly biosorbents to remove heavy metals from wastewater have been extensively studied. However, the chemical oxygen demand (COD) increase caused by the plant-derived biosorbent has not been considered previously. In this study, water hyacinth was used as biosorbent to remove Cd(II) from wastewater. About 66% of Cd(II) was removed by the biosorbent with a maximum biosorption capacity (qₘₐₓ) of 21.6 mg g⁻¹. However, the COD of the filtrate increased from 0 to 292 mg L⁻¹ during this process. Subsequently, endophytes, microalgae and the microalgae-endophyte symbiotic system (MESS) were assessed for the simultaneous Cd(II) and COD removal. Among these three systems, the MESS achieved the best performance. After 3 d of inoculation, the extent of total Cd(II) removal increased to 99.2% while COD decreased to 77 mg L⁻¹. This study provides a new insight into the application of a plant-derived biosorbent in combination with microalgae and endophytes for the effective treatment of heavy metal-bearing wastewater.

Due to the potential toxicity of polycyclic aromatic hydrocarbons (PAHs) to humans, the uptake and translocation of PAHs in food crops have gained much attention. However, it is still unclear whether phloem participates in the acropetal translocation of PAHs in plants. Herein, the evidence for acropetal translocation of phenanthrene (a model PAH) via phloem is firstly tested. Wheat (Triticum aestivum L.) new leaves contain significantly higher phenanthrene concentration than old leaves (P < 0.05), and the inhibitory effect on phenanthrene translocation is stronger in old leaves after abscisic acid and polyvinyl alcohol (two common transpiration inhibitors) application. Phenanthrene concentration in xylem sap is slightly higher than in phloem sap. Ring-girdling treatment can significantly reduce phenanthrene concentration in castor bean (Ricinus communis L.) leaves. Two-photon fluorescence microscope images indicate a xylem-to-phloem and acropetal phloem translocation of phenanthrene in castor bean stem. Therefore, phloem is involved in the acropetal translocation of phenanthrene in wheat seedlings, especially when the xylem is not mature enough in scattered vascular bundle plants. Our results provide a deeper understanding of PAH translocation in plants, which have significant implications for food safety and phytoremediation enhancement of PAH-contaminated soil and water.

Elasmobranchs are particularly prone to accumulating contaminants due to their life history patterns and relatively high trophic position. However, several compounds, especially contaminants of emerging concern, have still not been well studied in this group. Here, we aimed to determine the occurrence and concentrations of several inorganic and organic contaminants in different tissues of the Brazilian guitarfish Pseudobatos horkelii. This species is a critically endangered species, endemic from the Southwest Atlantic which uses southern Brazilian waters as a nursery habitat. Polycyclic aromatic hydrocarbons (PAHs), emerging pesticides, pharmaceutical and personal care products (PPCPs) and trace metals were determined in five biological tissues in order to assess the accumulation and organotropism of these compounds. Except for chlorothalonil and triclosan, all compounds were detected in, at least, one tissue, mostly in liver samples. All compounds differed among tissues, with liver presenting the higher concentrations of several contaminants, followed by muscle and gills. PAHs and PPCPs were the most detected analytes and presented the highest concentrations among tissues. Diclofenac levels were determined, for the first time in elasmobranchs, and were relatively high, when compared to other fishes. Finally, relatively high concentrations of PAHs, dichlofluanid and octocrylene in muscle might be suggestive of chronic exposure, presenting also human health implications. Regarding trace metals, contrary to most elasmobranch studies, Hg levels were low in all tissues, whereas Cd and Pb here higher in liver, and gills and blood samples, respectively. Our results indicate that P. horkelii is exposed to several organic and inorganic which might affect this species in a long-term scale. Concerning the determination of emerging contaminants, it is likely that other elasmobranchs are also exposed to these compounds and special attention should be given to this issue in order to predict future effects on this group.

Owing to environmental health concerns, a number of per- and polyfluoroalkyl substances (PFAS) have been phased-out, and increasingly replaced by various chemical analogs. Most prominent among these replacements are numerous perfluoroether carboxylic acids (PFECA). Toxicity, and environmental health concerns associated with these next-generation PFAS, however, remains largely unstudied. The zebrafish embryo was employed, in the present study, as a toxicological model system to investigate toxicity of a representative sample of PFECA, alongside perfluorooctanoic acid (PFOA) as one of the most widely used, and best studied, of the “legacy” PFAS. In addition, high-resolution magic angle spin (HRMAS) NMR was utilized for metabolic profiling of intact zebrafish embryos in order to characterize metabolic pathways associated with toxicity of PFAS. Acute embryotoxicity (i.e., lethality), along with impaired development, and variable effects on locomotory behavior, were observed for all PFAS in the zebrafish model. Median lethal concentration (LC₅₀) was significantly correlated with alkyl chain-length, and toxic concentrations were quantitatively similar to those reported previously for PFAS. Metabolic profiling of zebrafish embryos exposed to selected PFAS, specifically including PFOA and two representative PFECA (i.e., GenX and PFO3TDA), enabled elaboration of an integrated model of the metabolic pathways associated with toxicity of these representative PFAS. Alterations of metabolic profiles suggested targeting of hepatocytes (i.e., hepatotoxicity), as well as apparent modulation of neural metabolites, and moreover, were consistent with a previously proposed role of mitochondrial disruption and peroxisome proliferator-activated receptor (PPAR) activation as reflected by dysfunctions of carbohydrate, lipid and amino acid metabolism, and consistent with a previously proposed contribution of PFAS to metabolic syndrome. Taken together, it was generally concluded that toxicity of PFECA is quantitatively and qualitatively similar to PFOA, and these analogs, likewise, represent potential concerns as environmental toxicants.