Persistent Environmental Pollutants Research Articles

Environmental significance of PAH photoproduct formation: TiO2 nanoparticle influence, altered bioavailability, and potential photochemical mechanisms

Interactions between polycyclic aromatic hydrocarbons (PAHs) and titanium dioxide (TiO2) nanoparticles (NPs) can produce unforeseen photoproducts in the aqueous phase. Both PAHs and TiO2-NPs are well-studied and highly persistent environmental pollutants, but the consequences of PAH-TiO2-NP interactions are rarely explored. We investigated PAH photoproduct formation over time for benzo[a]pyrene (BaP), fluoranthene (FLT), and pyrene (PYR) in the presence of ultraviolet A (UVA) using a combination of analytical and computational methods including, identification of PAH photoproducts, assessment of expression profiles for gene indicators of PAH metabolism, and computational evaluation of the reaction mechanisms through which certain photoproducts might be formed. Chemical analyses identified diverse photoproducts, but all PAHs shared a primary photoproduct, 9,10-phenanthraquinone (9,10-PQ), regardless of TiO2-NP presence. The computed reaction mechanisms revealed the roles photodissociation and singlet oxygen chemistry likely play in PAH mediated photochemical processes that result in the congruent production of 9,10-PQ within this study. Our investigation of PAH photoproduct formation has provided substantial evidence of the many, diverse and congruent, photoproducts formed from physicochemically distinct PAHs and how TiO2-NPs influence bioavailability and time-related formation of PAH photoproducts.

From Antagonism to Enhancement: Triton X-100 Surfactant Affects Phenanthrene Interfacial Biodegradation by Mycobacteria through a Shift in Uptake Mechanisms.

Polycyclic aromatic hydrocarbons (PAHs), as persistent environmental pollutants, often reside in nonaqueous-phase liquids (NAPLs). Mycobacterium sp. WY10, boasting highly hydrophobic surfaces, can adsorb to the oil-water interface, stabilizing the Pickering emulsion and directly accessing PAHs for biodegradation. We investigated the impact of Triton X-100 (TX100) on this interfacial uptake of phenanthrene (PHE) by Mycobacteria, using n-tetradecane (TET) and bis-(2-ethylhexyl) phthalate (DEHP) as NAPLs. Interfacial tension, phase behavior, and emulsion stability studies, alongside confocal laser scanning microscopy and electron microscope observations, unveiled the intricate interplay. In surfactant-free systems, Mycobacteria formed stable W/O Pickering emulsions, directly degrading PHE within the NAPLs because of their intimate contact. Introducing low-dose TX100 disrupted this relationship. Preferentially binding to the cells, the surfactant drastically increased the cell hydrophobicity, triggering desorption from the interface and phase separation. Consequently, PAH degradation plummeted due to hindered NAPL access. Higher TX100 concentrations flipped the script, creating surfactant-stabilized O/W emulsions devoid of interfacial cells. Surprisingly, PAH degradation remained efficient. This paradox can be attributed to NAPL emulsification, driven by the surfactant, which enhanced mass transfer and brought the substrate closer to the cells, despite their absence at the interface. This study sheds light on the complex effect of surfactants on Mycobacteria and PAH uptake, revealing an antagonistic effect at low concentrations that ultimately leads to enhanced degradation through emulsification at higher doses. These findings offer valuable insights into optimizing bioremediation strategies in PAH-contaminated environments.

Global trends of dioxin and dioxin-like PCBs in animal-origin foods: a systematic review and gap areas

Global trends of dioxin and dioxin-like PCBs in animal-origin foods: a systematic review and gap areas

Polycyclic aromatic hydrocarbon skin permeation efficiency in vitro is lower through human than pigskin and decreases with lipophilicity

Polycyclic aromatic hydrocarbons (PAH) are persistent environmental pollutants, which occasionally appear as contaminants in consumer products. Upon dermal contact, transfer of PAH into the stratum corneum (s.c.) and migration through the skin may occur, resulting in this class of highly toxic compounds to become bioavailable. In this study, dermal penetration through human and porcine skin of 24 PAH, comprising broad mass (152–302 g/mol) and octanol-water partition coefficient (logP: 3.9–7.3) ranges, was evaluated via Franz diffusion cell in vitro assays. More lipophilic and potentially more toxic PAH had decreased permeation rates through the rather lipophilic s.c. into the more hydrophilic viable (epi-)dermis. Furthermore, human skin was less permeable than pigskin, a commonly used surrogate frequently applied in skin penetration studies. In particular, the s.c. of human skin retains a greater share of PAH, an effect that is more pronounced for smaller PAH. Moreover, we compared the skin permeation kinetics of different PAH in pigskin. While small PAH (< 230 g/mol, logP < 6) permeate the skin quickly and are detected in the receptor fluid after 2 h, large PAH (> 252 g/mol, logP ≥ 6) do not fully permeate the skin up to 48 h. This indicates that highly lipophilic PAH do not become bioavailable as readily as their smaller congeners when transferred to the skin surface. Our data suggest that pigskin could be used as a surrogate for worst case scenario estimates of dermal PAH permeation through human skin.

Facile synthesis of Au–TiO2/Bacterial cellulose aerogel nanocomposites with enhanced photocatalytic degradation of methylene blue under UV irradiation

The Au–TiO2/Bacterial cellulose aerogel nanocomposites (Au–TiO2/BC NCs) with remarkable photocatalytic properties and designed to solve agglomeration and reusability challenges in wastewater treatment have been successfully synthesized. The integration of gold nanoparticles (Au NPs) with TiO2, in conjunction with bacterial cellulose (BC) serving as a three-dimensional nanostructure, resulted in the formation of Au–TiO2/BC NCs through mechanical compositing, a confirmation obtained through various characterization techniques including XRD, SEM, SEM-EDS, TEM, TEM-EDS, BET, XPS, FT-IR, Spectrofluorometer, Raman, and UV–vis spectroscopy. The combination of Au–TiO2 nanoparticles with BC showcased homogeneous coverage over BC nanostructures, attributed to BC's unique properties, particularly its surface hydroxyl groups that prevent TiO2 agglomeration, along with uniform distribution of Au nanoparticles on TiO2 layers. Photocatalytic activity, assessed through methylene blue (MB) degradation under both UV and direct sunlight irradiation, demonstrated significantly improved efficiency with AuNPs, achieving approximately 90% degradation in the Au–TiO2/BC NCs under UV irradiation. The synthesized NCs exhibited stability with a slight performance reduction after cyclic tests, indicating potential for wastewater treatment applications under diverse light conditions. The integration of Au NPs onto TiO2 surfaces amplified light-induced reactions, addressing critical challenges in environmental remediation, particularly in the degradation of persistent environmental pollutants. This study offers valuable insights, positioning Au–TiO2/BC NCs as promising candidates for sustainable environmental remediation, emphasizing reusability, enhanced photocatalytic performance, and a straightforward synthesis process under both UV and direct sunlight irradiation.

Nanoremediation and Antioxidant Potential of Biogenic Silver Nanoparticles Synthesized Using Leucena's Leaves, Stem, and Fruits.

Synthetic dyes are persistent organic environmental pollutants that can cause extensive damage to living beings and to the ecosystem as a whole. Cost-effective, sustainable, and efficient strategies to deal with this type of pollution are necessary as it commonly resists conventional water treatment methods. Silver nanoparticles (AgNPs) synthesized using the aqueous extract from the leaves, stem, and fruits of Leucaena leucocephala (Leucena) were produced and characterized through UV-vis, TEM, EDS, SDL, XPS, XRD, and zeta potential, and they proved to be able to promote adsorption to remediate methylene blue and tartrazine pollution in water. The nanoremediation was performed and did not require direct exposure to sunlight or any special lamp or a specific reduction agent. The AgNPs produced using the extract from the leaves exhibited the best performance in nanoremediation and also presented antioxidant activity that surpassed the one from butylated hydroxytoluene (BHT). Consequently, it is an interesting nanotool to use in dye nanoremediation and/or as an antioxidant nanostructure.

Distribution of Pesticides and Polychlorinated Biphenyls in Food of Animal Origin in Croatia.

Pesticides and polychlorinated biphenyls (PCBs) are persistent environmental pollutants. When entering the food chain, they can represent a public health problem due to their negative effects on health. In this study, concentrations of organochlorine pesticides (OCPs), organophosphate pesticides (OPPs), pyrethroids, carbamates, and PCBs-a total 73 compounds-were determined in a total of 2268 samples of fat tissues (beef, pork, sheep, goat, poultry, game, horse, rabbit) and processed fat, meat, and processed meat products collected in Croatia during an 8-year period. In fatty tissues, 787 results exceeded the limits of quantification (LOQ): 16 OCPs, eight OPPs, six pyrethroids, one carbamate, and seven PCBs. The most positive results in fat samples were found for OCPs, with a frequency of quantification in the range of 57.5-87.5%. Hexachlorobenzene (HCB) and dichlorodiphenyldichloroethylene (DDE) were quantified in the highest percentages, in the ranges of 5.5-66.7% and 5.4-55.8%. Concentrations above the MRL values were determined for chlorpyrifos in pork fat and for resmethrin in six fat samples and one pâté. In 984 samples of meat and meat products, only 62 results exceeded the LOQ values. The highest frequency of quantification was determined for OCPs (25 samples), of which 40% were DDT isomers (60% DDE). Frequency quantifications of PCBs in fat samples were between 7.23 and 36.7%. An evaluation of the health risk assessment showed that the consumption of fat, meat, and meat products does not pose a threat to consumer health, since all EDI values were well below the respective toxicological reference values.

Evaluating contamination of seafood purchased from U.S. retail stores by persistent environmental pollutants, pesticides and veterinary drugs

Studies have reported health risks associated with seafood contamination, but few data exist on levels in commercially available seafood in the US. To better understand, the magnitude of foodborne exposure and identify vulnerable populations in the US, we measured concentrations of veterinary drugs, persistent organic pollutants (POPs) (polycyclic aromatic hydrocarbons [PAHs], polybrominated diphenyl ethers [PBDEs] and polychlorinated biphenyls [PCBs]), and legacy and current-use pesticides in 46 seafood samples purchased from retail outlets. Measured levels were used to estimate risk based on available maximum residue limits (MRLs) and toxic equivalence (TEQ) factors for analytes. Only seventeen of the 445 analytes were detected, at low substance frequencies. However, half of the samples tested positive for one or more analyte, with total concentrations ranging from below the limit of detection (LOD) to as high as 156 µg/kg wet weight. Based on the risk assessment for individual pesticides and veterinary drugs, the hazard quotients (HQ) were all <1, indicating no risk. However, for the sum of PCB126 and PCB167, two dioxin-like PCBs detected in our samples, the TEQ was nearly two orders of magnitude higher than the WHO limits in one catfish sample. Moreover, vulnerable groups with higher rates of consumption of specific fish types may face higher risks.

Degradation and metagenomic analysis of 4-chlorophenol utilizing multiple metal tolerant bacterial consortium.

Chlorophenols are persistent environmental pollutants used in synthesizing dyes, drugs, pesticides, and other industrial products. The chlorophenols released from these processes seriously threaten the environment and human health. The present study describes 4-chlorophenol (4-CP) degradation activity and metagenome structure of a bacterial consortium enriched in a 4-CP-containing medium. The consortium utilized 4-CP as a single carbon source at a wide pH range, temperature, and in the presence of heavy metals. The immobilized consortium retained its degradation capacity for an extended period. The 4-aminoantipyrine colorimetric analysis revealed complete mineralization of 4-CP up to 200mg/L concentration and followed the zero-order kinetics. The addition of glycerol and yeast extract enhanced the degradation efficiency. The consortium showed both ortho- and meta-cleavage activity of catechol dioxygenase. Whole genome sequence (WGS) analysis revealed the microbial compositions and functional genes related to xenobiotic degradation pathways. The identified genes were mapped on the KEGG database to construct the 4-CP degradation pathway. The results exhibited the high potential of the consortium for bioremediation of 4-CP contaminated sites. To our knowledge, this is the first report on WGS analysis of a 4-CP degrading bacterial consortium.

Isolation of High Density Polyethelene Degradating Bacteria from Soil

Plastics are the most commonly used polymers for routine applications. These plastics are less biodegradable in the environment. So the plastics accumulated drastically in the environment and had bad effects on it. High-density polyethylene (HDPE) is a major cause of persistent and long-term environmental pollution. The main objective of the present study is the isolation and screening of bacterial species with the capability to degrade high-density polyethylene (HDPE). The two bacterial isolates were identified from soil collected from the dumping yard of village Atake (Tal-Karad, Dist-Satara). These two bacterial isolates were obtained on minimal agar medium incorporated with HDPE. These isolates are further tested for degradation of the plastic. The isolate 1 (Bacillus cereus) could degrade the plastic to the extent of 16% in terms of % weight loss, while the isolate 2 (Pseudomonas halobacterium) could degrade the plastic to the extent of 10% in terms of % weight loss, thus the isolate 1, which was identified as Bacillus cereus was found to be the best among the two isolates.

Insight into the mechanism of melatonin in attenuating PCB126-induced liver injury: Resistance to ROS-dependent NETs formation to alleviate inflammation and lipid metabolism dysfunction

3,3′,4′,4′,5-Polychlorinated biphenyls (PCB126) is classified as a persistent organic environmental pollutant that can cause liver damage by producing excessive reactive oxygen species (ROS). ROS also can stimulate neutrophil extracellular traps (NETs) formation, which cause damage to organism if NETs are produced in excess. Melatonin is generally considered to possess strong antioxidant and anti-inflammation prosperities, but it is unclear whether it can alleviate PCB126-induced injury. To explore whether PCB126-induced liver injury is related to the formation of NETs and whether melatonin has a potent protective effect, we established PCB126 exposure/ PCB126 and melatonin co-treatment mouse models by gavage. To further clarify the specific mechanism, we also cultured neutrophils and AML12 cells to replicate in vivo model. Here, we found PCB126 exposure resulted in an elevation in the activities of MDA, LPO, PCO, and 8-OHdG, and a reduction in the activities of CAT, GSH-PX and SOD. We found that PCB126 exposure led to an elevation in the expression levels of chemokines (CCL2, CCL3, CCL4, CXCL12, and CXCL8) and marker factors for NETs formation (MPO, NE, NOX2, PKCα, and PKCζ) in the PCB126 group. IF, SYTOX staining, and SEM results also revealed that PCB126 could stimulate NETs formation. In addition, results of a co-culture system of PBNs and AML12 cells revealed that the expression levels of inflammatory cytokines (IL-1β, IL-6, and TNF-α) significantly decreased and the expression levels of metabolism factors (Fas, Acc, and Srebp) slightly decreased for scavenging NETs, indicating NETs formation aggravated PCB126-induced hepatic damages. Noteworthy, treatment with melatonin reversed these results. In summary, our findings revealed that melatonin alleviated hepatic damage aggravated by PCB126-induced ROS-dependent NETs formation through suppressing excessive ROS production. This finding not only enriches toxicological mechanism of PCB126, but more importantly extends biological effects of melatonin and its potential application values.

Microplastics cause hepatotoxicity in diabetic mice by disrupting glucolipid metabolism via PP2A/AMPK/HNF4A and promoting fibrosis via the Wnt/β-catenin pathway.

In recent years, microplastics (MPs) have gained significant attention as a persistent environmental pollutant resulting from the decomposition of plastics, leading to their accumulation in the human body. The liver, particularly of individuals with type 2 diabetes mellitus (T2DM), is known to be more susceptible to the adverse effects of environmental pollutants. Therefore, to investigate the potential impact of MPs on the liver of diabetic mice and elucidate the underlying toxicological mechanisms, we exposed db/db mice to 0.5 μm MPs for 3 months. Our results revealed that MPs exposure resulted in several harmful effects, including decreased body weight, disruption of liver structure and function, elevated blood glucose levels, impaired glucose tolerance, and increased glycogen accumulation in the hepatic tissue of the mice. Furthermore, MPs exposure was found to promote hepatic gluconeogenesis by perturbing the PP2A/AMPK/HNF4A signaling pathway. In addition, MPs disrupt redox balance, leading to oxidative damage in the liver. This exposure also disrupted hepatic lipid metabolism, stimulating lipid synthesis while inhibiting catabolism, ultimately resulting in the development of fatty liver. Moreover, MPs were found to induce liver fibrosis by activating the Wnt/β-catenin signaling pathway. Furthermore, MPs influenced adaptive thermogenesis in brown fat by modulating the expression of uncoupling protein 1 (UCP1) and genes associated with mitochondrial oxidative respiration thermogenesis in brown fat. In conclusion, our study demonstrates that MPs induce oxidative damage in the liver, disturb glucose and lipid metabolism, promote hepatic fibrosis, and influence adaptive thermogenesis in brown fat in diabetic mice. These findings underscore the potential adverse effects of MPs on liver health in individuals with T2DM and highlight the importance of further research in this area.

Effects of environmentally relevant concentrations of micro(nano)plastics on aquatic microorganisms: Changes in potential function but not in overall composition

Micro(nano)plastics (MNPs) are a growing problem as persistent environmental pollutants. Here, we investigated the impact of MNPs on microorganisms in aquatic microbial floc exposed to NPs (80 ​nm) and MPs (8 ​μm) for 35 days. Water quality indicators were tested weekly and microbiological analyses were conducted on Day 7 and 28 after exposure. The results showed that there were significant differences in the levels of total ammonia nitrogen or nitrite between the MNPs groups and the control group, spanning from Day 7 to Day 28. For the microbial response, microbial community richness in the NPs and MPs groups were significantly increased at Day 7. Functional prediction showed that the relative abundances of bacteria associated with the “Forms Biofilms”, “Potentially Pathogenic”, “Plastic Degradation” and nitrogen cycle processes were significantly different after MNPs exposure. The results suggest that MNPs had no significant effect on the microbial diversity of mature microbial flocs. Findings suggest MPs could cause an increase in the relative abundance of potentially pathogenic bacteria, while NPs do not. In addition, stress associated with MNPs affected the nitrogen cycle of microorganisms, and NPs exerted greater impacts than MPs. Findings from this study further our understanding of the impact of MNPs at environmentally relevant concentrations on microorganisms in aquatic ecosystems.

Rutin ameliorate PFOA induced renal damage by reducing oxidative stress and improving lipid metabolism

Perfluorooctanoic acid (PFOA) is a persistent environmental pollutant that can accumulate in the kidneys and eventually cause kidney damage. Rutin (RUTIN) is a natural flavonoid with multiple biological activities, and its use in against kidney damage has been widely studied in recent years. It is not yet known whether rutin protects against kidney damage caused by PFOA. In this study, 30 ICR mice were randomly divided into three groups: CTRL group, PFOA group and PFOA+RUTIN group. The mice were fed continuously by gavage for 28 days. Renal pathological changes were assessed by HE and PASM staining, and serum renal function and lipid indicators were measured. RNA-seq and enrichment analysis using GO, KEGG and PPI to detect differential expression of genes in treatment groups. Kidney tissue protein expression was determined by Western blot. Research has shown that rutin can improve glomerular and tubular structural damage, and increase serum CREA, HDL-C levels and decrease LDH, LDL-C levels. The expression of AQP1 and ACOT1 was up-regulated after rutin treatment. Transcriptomic analysis indicated that PFOA and rutin affect the transcriptional expression of genes related to lipid metabolism and oxidative stress, and may affected by PI3K-Akt, PPAR, NRF2/KEAP1 signaling pathways. In conclusion, rutin ameliorated renal damage caused by PFOA exposure, and this protective effect may be exerted by ameliorating oxidative stress and regulating lipid metabolism.

Per- and polyfluoroalkyl substances and cardiometabolic diseases: A review.

Per- and polyfluoroalkyl substances (PFAS) are a group of persistent and widespread environmental pollutants that represent a high concern for human health. They have been shown to be associated with several important physiological processes such as lipid metabolism and the immune system. Consequently, PFAS are suspected to play a role in cardiometabolic disease development. However, the evidence regarding associations between PFAS and overt cardiovascular disease and type 2 diabetes remains limited and inconsistent. To address this, we conducted a review of the epidemiological evidence. A deeper understanding of potential underlying molecular mechanisms may help to explain inconsistencies in epidemiological findings. Thus, to gain more mechanistic insight, we also summarized evidence from omics and laboratory studies into an adverse outcome pathway framework. Our observations indicate the potential for associations of PFAS with multiple molecular pathways that could have opposite associations with disease risk, which could be further modified by mixture composition, lifestyle factors or genetic polymorphisms. This identifies the need for exposome studies considering mixture effects, the use of multi-omics data to gain insight in relevant pathways and the integration of epidemiological and laboratory studies to enhance mechanistic understanding and causal inference. Improved comprehension is essential for environmental health risk assessments.

Accumulation of organophosphorus pollutants in adipose tissue of obese women - metabolic alterations

Organophosphorus pesticides (OPPs) and organophosphate esters (OPEs) are organophosphorus compounds created as substitutes for persistent environmental pollutants, namely organochlorines pesticides and brominated flame retardants, respectively. However, there is evidence that organophosphorus compounds are also widespread across the environment and have adverse effects on biota. In humans, OPPs and OPEs were reported to be carcinogenic, neurotoxic, hepatotoxic, nephrotoxic, amongst others. As lipophilic compounds, these accumulate in fat tissues as adipose tissue. Yet biomonitoring studies and analytical methodologies to assess these compounds in the human body are scarce, particularly in adipose tissue. In this study, the presence of six OPPs and seven OPEs was determined in samples of subcutaneous adipose tissue (scAT) and visceral adipose tissue (vAT) from 188 adult obese women. OPPs and OPEs were quantified by gas chromatography (GC) flame photometric detection and confirmed in GC tandem mass spectrometry. The detection frequencies ranged between 0.5-1.6% and 48–53%, respectively for OPPs and OPEs. Organophosphorus pollutants were present in both adipose tissues and median concentrations were 0.008 ± 0.020 μg/g scAT and 0.009 ± 0.020 μg/g vAT. A total of 32 Spearman's correlations were found between organophosphorus pollutants concentrations in adipose tissue and several biochemical parameters (18 positive and 14 negative). Our results show that anthropometric and hormonal parameters, cholesterol, glycaemia, macrominerals, urea and sedimentation velocity might be influenced by the presence of these compounds. The presence of organophosphorus pollutants in the environmental and their possible effect on female metabolic processes is concerning. Particularly because presently OPEs usage is not controlled or limited by any regulation. More studies are needed to fully understand these pollutants behaviour and hazard effects on human health, biota, and the environment so control regulations can be drawn to prevent and lessen their effects.

Influence of reactor composition on the thermal decomposition of perfluorooctanesulfonic acid (PFOS)

Various reactor tubes (quartz, stainless steel 316 and stainless steel 253 MA) were used to examine their influence on the thermal decomposition of perfluorooctanesulfonic acid (PFOS) between 400 and 1000 °C. Using helium as a carrier gas, with the addition of 100 – 300 ppm of PFOS to the feed gas, the influence of the reactor materials on PFOS decomposition was studied. The quartz reactor led to a notable reduction in the concentration of HF and substantial quantities of SiF4 were observed. Stainless steel 316 produced C2F4, HF, COF2 and SO2 as its primary products up to 800 °C. However, at temperatures above 800 °C, near quantitative removal of SO2 from the gas phase was observed, with the concomitant formation of a blue molybdenum sulfur complex. Stainless steel 253 MA, the composition of which contains over 1% Si produced substantial quantities of SiF4 but no significant decrease in the gas phase concentration of HF. Environmental implicationThis research underscores the significant role of reactor material in the thermal treatment of PFAS, a globally widespread and enduring environmental contaminant. The findings have direct implications for the optimization of thermal treatment strategies aimed at mitigating PFAS contamination. The insight into how different reactor materials interact with PFOS during thermal treatment expands our understanding of potential destruction methods. This knowledge is crucial in the development of effective, sustainable strategies for managing persistent environmental pollutants like PFAS.

Biodegradation of Benzo[a]pyrene by a White-Rot Fungus Phlebia acerina: Surfactant-Enhanced Degradation and Possible Genes Involved.

Polycyclic aromatic hydrocarbons (PAHs) are persistent environmental pollutants that pose a threat to human health. Among these PAHs, benzo[a]pyrene (BaP), a five-ring compound, exhibits high resistance to biodegradation. White-rot fungus Phlebia acerina S-LWZ20190614-6 has demonstrated higher BaP degradation capabilities compared with Phanerochaete chrysosporium and P. sordida YK-624, achieving a degradation rate of 57.7% after 32 days of incubation under a ligninolytic condition. To further enhance the biodegradation rate, three nonionic surfactants were used, and the addition of 1 or 2 g·L-1 of polyethylene glycol monododecyl ether (Brij 30) resulted in nearly complete BaP biodegradation by P. acerina S-LWZ20190614-6. Interestingly, Brij 30 did not significantly affect the activity of manganese peroxidase and lignin peroxidase, but it did decrease laccase activity. Furthermore, the impact of cytochrome P450 on BaP degradation by P. acerina S-LWZ20190614-6 was found to be relatively mild. Transcriptomic analysis provided insights into the degradation mechanism of BaP, revealing the involvement of genes related to energy production and the synthesis of active enzymes crucial for BaP degradation. The addition of Brij 30 significantly upregulated various transferase and binding protein genes in P. acerina S-LWZ20190614-6. Hence, the bioremediation potential of BaP by the white-rot fungus P. acerina S-LWZ20190614-6 holds promise and warrants further exploration.

Algae-Enhanced Electrospun Polyacrylonitrile Nanofibrous Membrane for High-Performance Short-Chain PFAS Remediation from Water.

As a short-chain PFAS (per- and polyfluoroalkyl substance), GenX was produced in recent years to replace traditional long-chain PFASs, such as perfluorooctanoic acid (PFOA). However, GenX turns out to be more toxic than people originally thought, posing health risks as a persistent environmental pollutant. In this research, for the first time, we incorporated chlorella, a single-celled green freshwater microalga that grows worldwide, with polyacrylonitrile (PAN) in equal amounts in electrospun nanofibers and studied the capability of the electrospun PAN/Algae bicomponent nanofibrous membrane (ES(PAN/Algae)) to bind and remove GenX from water. The incorporation of algae demonstrated a synergistic effect and significantly improved the GenX removal efficiency of the nanofibrous membrane. The maximum GenX removal capacity reached 0.9 mmol/g at pH 6, which is significantly higher than that of most of the reported GenX adsorbents as well as activated carbon. The GenX removal mechanism was investigated and discussed by using water contact angle, zeta potential, FTIR, and XPS techniques. This research demonstrated the potential to make highly efficient adsorbent/filter materials from common and economic materials to practically remediate short-chain PFASs from various water bodies.

Mulch-derived microplastic aging promotes phthalate esters and alters organic carbon fraction content in grassland and farmland soils

Agricultural plastic mulch is a major microplastics (MPs) source in terrestrial ecosystems. However, knowledge about the aging characteristics of mulch-derived MPs entering natural and agricultural soils and their effects on phthalate esters (PAEs) and organic carbon fractions is still limited. Black (contains black masterbatches) and white polyethylene (PE) and biodegradable (Bio, Poly propylene carbonate and Polybutylene adipate terephthalate synthetic material (PPC+PBAT)) mulch-derived MPs, at 0.3% (w/w) dose, were added to grassland and farmland soils for eight-week incubation. Microplastic (MP) aging degree was explored by quantifying the carbonyl index (CI). The soil PAEs and organic carbon fractions were also analyzed. After incubation, black and white PE-MP aged greater in farmland than in grassland. PAEs accumulated highest in PE-MP treatment (5.27–6.41 mg kg−1) followed by Bio-MP (1.88–2.38 mg kg−1). Soil organic carbon (SOC), particulate organic carbon (POC), and microbial biomass carbon (MBC) were reduced by 5.3%–8.2%, 31.8%–41.6%, and 39.7%–63.0%, dissolved organic carbon (DOC) was increased by 10.1%–27.6% in grassland containing MP compared to control. MPs’ aging degree promoted PAEs content or altered nutrients, then regulated soil microbial biomass and extracellular enzyme activity directly or indirectly, ultimately affecting SOC. Environmental implicationMicroplastics are persistent environmental pollutants that gradually undergo surface aging in response to extracellular enzymes secreted by microorganisms. As microplastics age, their surface roughness and functional groups change; thus, organochemical contaminants gradually leach out. Therefore, this study analyzed the aging of mulch film-derived microplastics under the action of diverse microorganisms in farmland and grassland soils and the effect on plasticizer and organic carbon fractions. The results proved that polyethylene microplastic aging degree was highest in farmland soil. Besides, biodegradable microplastic caused lower contamination of phthalate esters than polyethylene, but they affected soil carbon balance in grassland and farmland soils. Statement of environmental implicationThis study highlights that MPs affect organic carbon fractions by influencing the PAEs, available nutrients, and extracellular enzyme activity.