Persistent Pollutants Research Articles

Obesogens and Energy Homeostasis: Definition, Mechanisms of Action, Exposure and Adverse Effects on Human Health.

Obesity is a major risk factor for noncommunicable diseases and is associated with a reduced life expectancy of up to 20 years, as well as with other consequences such unemployment and increased economic burden for society. It is a multifactorial disease and physiopathology of obesity involves dysregulated calorie utilization and energy balance, disrupted homeostasis of appetite and satiety, lifestyle factors including sedentary lifestyle, lower socio-economic status, genetic predisposition, epigenetics and environmental factors. Some endocrine-disrupting chemicals (EDCs) have been proposed as "obesogens" that stimulate adipogenesis leading to obesity. In this review, definition of obesogens, their adverse effects, underlying mechanisms and metabolic implications will be updated and discussed. Disruption of lipid homeostasis by EDCs involves multiple mechanisms including increase in the number and size of adipocytes, disruption of endocrine-regulated adiposity and metabolism, alteration of hypothalamic regulation of appetite, satiety, food preference and energy balance, and modification of insulin sensitivity in the liver, skeletal muscle, pancreas, gastrointestinal system and the brain. At a cellular level, obesogens can exert their endocrine disruptive effects by interfering with peroxisome proliferator-activated receptors and steroid receptors. Human exposure to chemical obesogens mainly occurs by ingestion and, to some extent, by inhalation and dermal uptake, usually in an unconscious manner. Persistent pollutants are lipophilic features; thus, they bio-accumulate in adipose tissue. Although there is an increasing number of reports studying the effects of obesogens, their mechanisms of action remain to be elucidated. In addition, epidemiological studies are needed in order to evaluate human exposure to obesogens.

Using diatom chain length as a bioindicator of heavy-metals contamination in marine environments

The increasing release of toxic heavy metals into marine environments poses significant risks due to their persistence and bioaccumulation. Diatoms are ideal bioindicators because of their sensitivity to environmental changes. Despite traditional methods for detecting these persistent pollutants effectively identify composition and concentration, they are time-consuming, they often require the use of harmful reagents, and do not allow a fast assessment of detrimental impacts on marine organisms. To fill this gap, we have successfully investigated the toxicity of different heavy metals in the marine diatom Skeletonema pseudocostatum thanks to a newly developed high-power terahertz (THz) spectrometer. By combining THz spectroscopy, microscopy and ecotoxicological assays, we found that the formation of long diatom chains is significantly inhibited by the presence of lead, copper, and chromium, which disrupt their metabolism. Although the THz absorption and refractive index spectra were not affected by diatom concentration in undoped samples, THz frequencies were highly sensitive to changes in diatom chain length due to heavy metals exposure. These findings suggest that this approach allows to investigate the biochemical processes involved in chain formation in S. pseudocostatum and related algae. THz spectroscopy could therefore provide deeper insights into the microscopic metabolic activity of diatoms, addressing key biochemical questions surrounding these organisms. Furthermore, we propose this novel approach for environmental pollution monitoring, since it could provide a rapid, harmless and sensitive detection method to assess heavy metal toxicity in marine diatoms, key organisms at the basis of the trophic chain.

Development and characterization of active gelatin-chitosan packaging incorporated with guava leaf extract for extending meat shelf life

Biopolymer films (biofilms) were evaluated for suitability in meat packaging applications. Polyesters, proteins, and carbohydrates are among the most commonly utilized materials for producing bioplastics due to their mechanical properties, which closely resemble those of conventional plastics. However, these properties are significantly influenced by the film's composition, molecular weight, solvent type, pH, component concentration, and processing temperature. Conventional plastic films, including microplastics, are non-bioactive and contribute to persistent pollution. This underscores the importance of developing novel materials that incorporate bioactive plant compounds to endow plastic films with antimicrobial and antioxidant functionalities. In this study, two gelatin-chitosan films were fabricated: one without any extract and another incorporating guava leaf extract. These films were characterized to determine their optical, mechanical, morphological, and thermal properties. Additionally, a microbiological analysis was conducted to assess the impact of polymeric biofilm packaging on the shelf life of beef. Both films exhibited favorable tensile strength values (24.74 – 27.12 MPa), high transparency (0.79 – 1.18), and effective barrier properties against water vapor (8.95 – 9.29 × 10⁻⁸ g·mm·Pa⁻1·h⁻1·m⁻2) and oxygen (9.7–9.10 × 10⁻1⁸ m³·m⁻2·s⁻1·Pa⁻1). During storage, the biofilm containing guava leaf extract demonstrated a reduction in microbial growth, and this enhanced the beef’s color stability. In conclusion, biopolymeric films incorporating guava leaf extract demonstrated notable antioxidants and antimicrobial properties, effectively inhibiting microbial growth, preserving the physical quality of beef, and significantly extending its shelf life under refrigerated conditions.

New weapons explosive exhibits persistent toxicity in plants.

Explosives are widespread, toxic and persistent environmental pollutants. 2,4-Dinitroanisole (DNAN) is being phased in to replace 2,4,6-trinitrotoluene (TNT) in munitions. Here we demonstrate that only low levels of DNAN are detoxified in Arabidopsis, leaving it to remain as a substrate for monodehydroascorbate reductase 6 mediated chronic phytotoxicity. Enhancing the potential for environmental toxicity, DNAN is readily transported to the aerial tissues exposing this toxin to herbivores and the wider food chain.

Biophotoelectrocatalytic detoxification of Bisphenol A using Bismuth-doped TiO2 Nanotubes photoanode coupled with Laccase-immobilized cathode

Photoelectrocatalytic (PEC) technology has been demonstrated to be an effective method for environmental remediation, but its efficiency in detoxifying persistent pollutants such as bisphenol A (BPA) requires further enhancement. Herein, an enzyme-coupled PEC system for detoxification of BPA was proposed by integrating a Bismuth-doped TiO2 Nanotubes (Bi-TiO2 NTs) photoanode and laccase-immobilized cathode. The results reveal that the doping of Bi into TiO2 enhances the visible light absorption and reduces the recombination of photogenerated electron-hole pairs when exposed to simulated solar irradiation. When the laccase-immobilized cathode was incorporated into the PEC device, the resulting biophotoelectrocatalytic system exhibited excellent degradation performance for BPA, owing to the synergistic effect between enzymatic catalysis and photoelectrocatalysis. A potential degradation pathway for BPA was established through the analysis of intermediate products, and subsequent phytotoxicity assessments revealed a significant reduction in the toxicity of the laccase-coupled PEC-degraded BPA solution. This study highlights that coupling a laccase-immobilized cathode with Bi-doped TiO2 NTs photoanodes serves as an effective method for the detoxification of persistent pollutants.

Analysis of perfluoroalkyl carboxylates and perfluoroalkyl sulfonates in environmental water by in-port arylation gas chromatography-electron impact ionization-mass spectrometry.

Per- and polyfluoroalkyl substances (PFAS) are persistent environmental pollutants that have been used for various purposes. Although PFAS can pollute the environment in a variety of areas related to the use, storage, and disposal of their products, there are insufficient data on the extent of PFAS pollution outside industrialized countries with their manufacturing facilities. Most of the analyses depend on high-cost liquid chromatography-tandem mass spectrometry. In this study, we established a method to analyze ionic PFAS using gas chromatography-electron impact ionization-mass spectrometry with in-port arylation by diaryl iodonium. Extraction of PFAS from water samples was performed using solid phase extraction with reverse phase sorbent. Fourteen PFAS compounds could be detected from spiked water samples, and the detection limit ranged from 3.1 to 8.1ng L-1. Using this method, we analyzed groundwater samples from Okinawa Island, Japan, and detected PFAS up to a total concentration of 1900ng L-1. This method uses relatively inexpensive analytical equipment; hence, it can possibly enable surveys on PFAS contaminations in a wide range of regions and opportunities.

Heavy metals: toxicity and human health effects.

Heavy metals are naturally occurring components of the Earth's crust and persistent environmental pollutants. Human exposure to heavy metals occurs via various pathways, including inhalation of air/dust particles, ingesting contaminated water or soil, or through the food chain. Their bioaccumulation may lead to diverse toxic effects affecting different body tissues and organ systems. The toxicity of heavy metals depends on the properties of the given metal, dose, route, duration of exposure (acute or chronic), and extent ofbioaccumulation. The detrimental impacts of heavy metals on human health are largely linked to their capacity to interfere with antioxidant defense mechanisms, primarily through their interaction with intracellular glutathione (GSH) or sulfhydryl groups (R-SH) of antioxidant enzymes such as superoxide dismutase (SOD), catalase, glutathione peroxidase (GPx), glutathione reductase (GR), and other enzyme systems. Although arsenic (As) is believed to bind directly to critical thiols, alternative hydrogen peroxide production processes have also been postulated. Heavy metals are known to interfere with signaling pathways and affect a variety of cellular processes, including cell growth, proliferation, survival, metabolism, and apoptosis. For example, cadmium can affect the BLC-2 family of proteins involved in mitochondrial death via the overexpression of antiapoptotic Bcl-2 and the suppression of proapoptotic (BAX, BAK) mechanisms, thus increasing the resistance of various cells to undergo malignant transformation. Nuclear factor erythroid 2-related factor 2 (Nrf2) is an important regulator of antioxidant enzymes, the level of oxidative stress, and cellular resistance to oxidants and has been shown to act as a double-edged sword in response to arsenic-induced oxidative stress. Another mechanism of significant health threats and heavy metal (e.g., Pb) toxicity involves the substitution of essential metals (e.g., calcium (Ca), copper (Cu), and iron (Fe)) with structurally similar heavy metals (e.g., cadmium (Cd) and lead (Pb)) in the metal-binding sites of proteins. Displaced essential redox metals (copper, iron, manganese) from their natural metal-binding sites can catalyze the decomposition of hydrogen peroxide via the Fenton reaction and generate damaging ROS such as hydroxyl radicals, causing damage to lipids, proteins, and DNA. Conversely, some heavy metals, such as cadmium, can suppress the synthesis of nitric oxide radical (NO·), manifested by altered vasorelaxation and, consequently, blood pressure regulation. Pb-induced oxidative stress has been shown to be indirectly responsible for the depletion of nitric oxide due to its interaction with superoxide radical (O2·-), resulting in the formation of a potent biological oxidant, peroxynitrite (ONOO-). This review comprehensively discusses the mechanisms of heavy metal toxicity and their health effects. Aluminum (Al), cadmium (Cd), arsenic (As), mercury (Hg), lead (Pb), and chromium (Cr) and their roles in the development of gastrointestinal, pulmonary, kidney, reproductive, neurodegenerative (Alzheimer's and Parkinson's diseases), cardiovascular, and cancer (e.g. renal, lung, skin, stomach) diseases are discussed. A short account is devoted to the detoxification of heavy metals by chelation via the use of ethylenediaminetetraacetic acid (EDTA), dimercaprol (BAL), 2,3-dimercaptosuccinic acid (DMSA), 2,3-dimercapto-1-propane sulfonic acid (DMPS), and penicillamine chelators.

Exploring the sources, occurrence, transformation, toxicity, monitoring, and remediation strategies of per- and polyfluoroalkyl substances: a review.

Per- and polyfluoroalkyl substances (PFAS), a class of man-made chemicals, possess unique properties that have rendered them indispensable in various industries and consumer goods. However, their extensive use and persistence in the environment have raised concerns about their potential repercussions on human health and the ecosystem. This review provides insights into the sources, occurrence, transformation, impacts, fate, monitoring, and remediation strategies for PFAS. Once released into the environment, these chemicals undergo intricate transformation processes, such as degradation, bioaccumulation, and biomagnification, which result in their far-reaching distribution and persistence. Their chemical stability results in persistent pollution, with far-reaching ecological and human health implications. Remediation strategies for PFAS are still in their infancy, and researchers are exploring innovative and sustainable methods for treating contaminated environments. Promising technologies such as adsorption, biodegradation, and electrochemical oxidation have shown the potential to remove PFAS from contaminated sites, yet the search for more efficient and sustainable solutions continues. In conclusion, this review emphasizes the urgent need for continued research and innovation to address the global environmental challenge posed by PFAS. As we move forward, it is imperative to prioritize sustainable solutions that minimize the detrimental consequences of these substances on human health and the environment.

Numerical study of rainfall percolation through a novel capillary barrier cover with a zipper-shape interface between fine- and coarse-grained soils

The huge amount of leachate generated in landfills causes persistent pollution to soil and groundwater. Landfill cover is vital for reducing leachate generation through reducing rainwater infiltration. Yet, the traditional cover with capillary barrier effects (CCBE) is only applicable in reducing rainwater percolation at its base in arid or semi-arid region. To solve this problem, a novel capillary barrier cover is proposed, which adds multiple gravel-segments to the traditional CCBE to form the zipper-shape interface between fine- and coarse-grained soils. Hydraulic response of this zippered CCBE is numerically investigated considering different gravel-segment sizes, drainage-ditch widths and climate conditions. It is found that the zippered CCBE has a lower water percolation than the traditional one by up to 57 %. It is because the capillary barrier effects along the right side-wall of gravel-segment leads to water accumulation and hence water percolation near its base, facilitating reducing water percolation using drainage ditch below the gravel-segment. Moreover, water percolation increases when the gravel-segment height exceeds 0.3 times thickness of fine-grained soil or the gravel-segment width increases, due to reduction of water storage in fine-grained soil. Under the recorded annual precipitation of 1235 mm in the semi-humid region in China, the annual percolation of the traditional and zippered CCBEs are 84 mm/year and 36 mm/year, respectively. Thus, the zippered CCBE might extent the applicability of the traditional CCBE from arid or semi-arid region to semi-humid region.

Construction of Mo-Doped CuO Incorporated on Carbon Black Modified Disposable Sensor for the Voltammetric Detection of Metol in Environmental Samples

Abstract In this study, a molybdenum-doped copper oxide (Mo–CuO) composite was synthesized via a hydrothermal method and combined with carbon black (CB) to form Mo–CuO@CB. This composite was used to modify a screen-printed carbon electrode (SPCE) for the detection of Metol (MT), an industrial pollutant harmful to both human health and the environment. Structural and surface characterization was performed using high-resolution transmission electron microscopy, field-effect scanning electron microscopy, energy-dispersive spectroscopy, Raman spectroscopy, X-rssy photoelectron spectroscopy, and X-ray diffraction. Electrochemical techniques, including differential pulse voltammetry and cyclic voltammetry, were used to assess the sensor's performance. The Mo–CuO@CB@SPCE sensor exhibited a low detection limit of 2.7 nM, and limit of quantification is 82 nM, a broad linear range (5.0 × 10−9 – 170 mol L-1), and high sensitivity (4.148 μA μM⁻¹ cm⁻²), benefiting from the catalytic activity of Mo–CuO and the large surface area of CB. With recovery rates ranging from 96 % to 100.6% in pond, river, and tap water, the sensor effectively detects MT in environmental samples, ensuring reliable monitoring of this persistent pollutant.

Impact of Legacy Perfluorooctane Sulfonate (PFOS) and Perfluorooctanoate (PFOA) on GABA Receptor-Mediated Currents in Neuron-Like Neuroblastoma Cells: Insights into Neurotoxic Mechanisms and Health Implications.

Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are persistent environmental pollutants, raising concerns due to their widespread presence and disruptive biological effects. These compounds are highly stable, allowing them to bioaccumulate in the environment and living organisms, potentially impacting critical physiological functions such as hormonal balance, immune response, and increasing cancer risk. Despite regulatory restrictions, their pervasive nature necessitates further research into their potential effects on cellular and neuronal function. This study first evaluated the cytotoxic effects of PFOS and PFOA on S1 neuroblastoma cells; a dose-dependent reduction in cell viability was revealed for PFOS, while PFOA exhibited minimal toxicity until millimolar concentrations. We further investigated their potential to modulate GABAergic neurotransmission using patch-clamp electrophysiology. Both PFOS and PFOA caused a significant but reversible reduction in GABA receptor-mediated currents following one-minute pre-treatment. These findings suggest that PFOS and PFOA can interfere with both cellular viability and GABAergic signaling, providing critical insights into their functional impacts and highlighting the need for further investigation into the long-term consequences of PFAS exposure on nervous system health.

Visible light responsive heterophase Titania monoliths for the fast and efficient photocatalytic decontamination of organic pollutants

The article reports the synthesis of an ordered mesoporous network of heterophase TiO2 monoliths as a visible light-responsive photocatalyst using tri-block copolymers of Pluronic F108, P123 and F127 as structure-directing agents (SDAs) and temperature-controlled calcination (450–650 °C) has been carried out by direct templating-assisted hydrothermal approach. The structural/surface morphology and topographical properties of the photocatalyst are characterized using FE-SEM-EDAX, HR-TEM-SAED, p-XRD, VB-XPS, PLS, TG/DTA, UV-Vis-DRS, BET/BJH and zeta potential analysis. The undoped heterophase mesoporous TiO2 monoliths with in-built lattice/surface defects exhibit visible light photocatalytic properties, successfully dissipating Reactive Brown 10 (RB-10) dye. The influence of physicochemical parameters, such as SDAs, temperature, pH, dye concentration, catalyst dosage, photosensitizers and light intensities, are optimized for maximum photocatalytic performance at a shorter timespan. The F127-assisted mesoporous TiO2 monolith (550 °C) exhibits superior degradation kinetics (15 min) for RB-10 dye solution (20 ppm) at pH 2.0–3.0 using a photocatalyst dosage of 50 mg and 2 mM of KBrO3, irradiated with 150 W/cm2 tungsten lamp. The photocatalysts are fabricated without complicated chemical modifications and display topmost efficiency in quickly decontaminating persistent pollutants. The photoproducts from RB-10 photocatalytic degradation are investigated using HR-MS analysis. The photocatalyst can be reused efficiently for six cycles, even under extreme conditions.

Unraveling the promotive mechanism of nitrogen-doped porous carbon from wasted lignin for Cr (VI) removal

Persistent environmental pollution by heavy metals, particularly Cr (VI), poses significant risks to ecosystems and human health due to its high toxicity and bioaccumulation potential. The development of high-performance, cost-effective adsorbents from sustainable materials remains a critical challenge in the field of Cr (VI) remediation. This study investigates the influence of pyrrolic-N (N-5) within nitrogen-doped hierarchical porous carbon (N-HPC) on its adsorption capacity. Results indicate that N-HPC variants with a higher N-5 content exhibit superior adsorption abilities. The optimal sample demonstrated an exceptional adsorption capacity of 386.2 mg/g for Cr (VI). Even after seven regeneration cycles, this N-HPC variant maintained a remarkable 77.8 % removal efficiency for Cr (VI), highlighting its robust stability and selectivity. The relationship between the physicochemical properties of N-5 and N-HPC was thoroughly examined, revealing that N-5 plays a crucial role in the adsorption process. Due to its high electronegativity, nitrogen-doping into the carbon framework generates a dipole moment, enhancing the electronegativity of N-HPC, altering its local electron density and polarity, increasing specific surface area, carbon defect density, and ion exchange capacity. These factors collectively contribute to significant improvements in pore filling, ion exchange efficiency, and electrostatic adsorption by N-HPC. The reduction complexation mechanism emerges as the dominant factor in the adsorption process. N-5 not only provides reducing electrons as an electron donor, facilitating the continuous conversion of Cr (VI) to Cr (III), but also acts as an adsorption active site, complexing Cr to the surface of N-HPC. This synergistic effect strengthens the reduction complexation, enhances adsorption performance, and improves the regeneration cycle and adsorption selectivity for Cr.

Ecotoxicological Impact of Cigarette Butts on Coastal Ecosystems: The Case of Marbella Beach, Chile

Cigarette butts (CBs) are a major source of persistent pollution in coastal ecosystems, introducing harmful chemicals and microplastics into the environment. This study assesses the ecotoxicological impact of CB leachates on Marbella Beach, Chile, by analyzing the metal contamination and its phytotoxic effects on Lactuca sativa and Lolium perenne. Three scenarios were evaluated: CBs alone, CBs mixed with sand, and sand alone. Leachate analysis revealed significant concentrations of iron and zinc, with higher toxicity observed in scenarios involving CBs. Ecotoxicological assays demonstrated that cigarette butt leachates severely inhibited seed germination and plant growth, particularly in Lactuca sativa, which showed greater sensitivity compared to that of Lolium perenne. The results underscore the partial mitigating role of sand, although it was insufficient to prevent the toxic effects of CBs. The persistence of cellulose acetate in the environment and the continued release of hazardous chemicals highlight the ecological risks posed by cigarette butt pollution. These findings emphasize the need for improved waste management strategies and the development of biodegradable cigarette filters to reduce environmental contamination in coastal areas.

Recent trends in remediating Basic Red 46 dye as a persistent pollutant from water bodies using promising adsorbents: a review

Recent trends in remediating Basic Red 46 dye as a persistent pollutant from water bodies using promising adsorbents: a review

Polysaccharides and Composite Adsorbents in the Spotlight for Effective Agrochemical Residue Removal from Water

Agrochemical residues, including pesticides and herbicides, pose significant environmental and health risks when present in water sources. Conventional water treatment methods often fall short in effectively removing these persistent pollutants, necessitating innovative solutions. This review explores the use of polysaccharides and composite adsorbents as sustainable alternatives for agrochemical residue removal from water. Biopolymers such as chitosan, alginate, and cellulose are highlighted for their biodegradability, biocompatibility, and ability to be functionalized for enhanced adsorption performance. Recent advances in the development of composite materials incorporating nanomaterials, such as graphene, oxide, and metal oxides, have shown significant promise in enhancing the efficiency and selectivity of agrochemical adsorption. The review also addresses the fundamental mechanism of adsorption, such as electrostatic interactions, hydrogen bonding, and hydrophobic forces, that contribute to the effectiveness of these materials. Challenges associated with scalability, regeneration, and real-world applications are discussed, as well as future opportunities for integrating emerging technologies like 3D printing and machine learning into adsorbent design. Overall, polysaccharides and composites offer a promising pathway toward achieving efficient and sustainable agrochemical residue removal, with ongoing research needed to overcome current limitations and optimize their practical application in water treatment.

Vulnerability of kelp, Ecklonia radiata, to persistent nitrogen pollution and coastal darkening

Coastal darkening is expected to have pervasive impacts on benthic primary producers. However, the effects of nitrogen enrichment, an often-co-occurring stressor, on benthic primary producers and their functions is less clear. This study investigates the interactive effects of coastal darkening and nitrogenous eutrophication, including nitrogen source (NH4+ vs. NO3−), on the function of the kelp Ecklonia radiata. First, an in-situ experiment was used to assess the differential impacts of NH4+ and NO3− pulse enrichment on the photosynthetic performance and pH modulation capacity of E. radiata. Second, a laboratory experiment was used to assess the longer-term impacts of nitrogen enrichment under low-light conditions mimicking coastal darkening on service provisioning, including photosynthetic performance, pH modulation, nutrient uptake and growth. While pulse nitrogen enrichment had no impacts on the photosynthetic performance of E. radiata in-situ, persistent exposure to either NH4+ or NO3− acted as a stressor to sporophytes as indicated by elevated rates of dark respiration and lamina erosion and reduced photosynthetic efficiency and growth rates. Furthermore, low-light conditions elicited reduced photosynthetic capacity at saturating irradiance, which extended to a reduction in the extent of pH modulation, and significantly increased lamina erosion. While the two stressors appeared to act on distinct parameters, ultimately, both darkening and eutrophication directly reduced net primary production, especially when in combination. These results demonstrate the negative interactive effects of coastal darkening and eutrophication on E. radiata function, while suggesting a vulnerability of E. radiata to even moderate levels of persistent nitrogen enrichment. This vulnerability highlights the need to consider environmental conditions during kelp conservation and restoration, and when attempting to valorise kelp ecophysiology for nature-based solutions.

Polyethylene microplastic modulates the toxicity of pentachlorophenol to the microalgae Isochrysis galbana, clone t-ISO

Pentachlorophenol (PCP) and polyethylene microplastic (PE-MP) have been designated as emerging and persistent pollutants, respectively. The combined effects of those pollutants are still unknown, especially to organisms like phytoplankton that may adsorb to their surface. Therefore, the purpose of this study was to investigate for the first time the effects of PE-MP alone and in combination with PCP on the microalgae Isochrysis galbana, clone t-ISO following 72 h of exposure. Photosynthetic pigments amounts, carotenoid, protein, carbohydrate and fatty acids have been assessed. Acute toxicity test showed that the 72 h median inhibition concentration (72 h-EC50) was 148.2, 0.66 and 087 mg L−1 for PE-MP, PCP and their mixture. The utmost effects in growth inhibition rates were noted with 0.5 and 1.25 mg L−1 PCP (23% and 85%, respectively), and 100 and 300 mg L−1 PE-MP (49% and 64%, respectively). Moreover, it was found that those concentrations had a major impact on the photosynthetic pigments, protein, carbohydrate, and fatty acids amounts in algal cells. Furthermore, levels of H2O2 and Malondialdehyde (MDA), as well as the activities of catalase (CAT), superoxide dismutase (SOD), and ascorbate peroxidase (APX), indicated the induction of an oxidative stress in algal cells. It appears that adding PE-MP at a no-effect concentration (25 mg L−1) reduces the toxicity caused by PCP due to its adsorption to polyethylene microplastics.

Insights into sulfamethazine degradation by peroxymonosulfate activation using H2 reduced hematite in high-salinity wastewater: Performances and mechanisms

Sulfamethazine (SMT) is recognized as a persistent, bioaccumulate, and toxic antibiotic pollutant that is difficult to be completely eliminated through traditional wastewater treatment methods. Although advanced oxidation processes (AOPs) utilizing peroxymonosulfate (PMS) have demonstrated potential in degrading SMT, the lack of inexpensive and efficient PMS activators remains a significant obstacle for its practical application. In this study, we present the synthesis of a highly effective PMS activator, the naturally-occurring minerals-based material − H2– reduced hematite (HRH), on an industrial scale using a fluidized bed reactor. Impressively, within the PMS AOPs system, the synthesized HRH catalyst not only achieves 99.3 % degradation of SMT within 20 min, demonstrating a remarkable 10-fold increase in the degradation rate compared to pristine hematite, but also showcases excellent recyclability and durability. Additionally, this HRH/PMS system were proved to effectively remove SMT under high-salinity conditions. More importantly, through systematic characterization and theoretical calculations, an in-depth investigation into the primary activation mechanism and degradation pathway in this reaction process is provided. This work provided a highly feasible strategy for the application of natural mineral-based catalyst for the degradation of pollutants via PMS activation in high-salinity wastewater.

Association between exposure to per- and polyfluoroalkyl substances and missed miscarriage: A hospital-based case-control study in Shanghai, China

Per- and polyfluoroalkyl substances (PFAS) are persistent environmental pollutants linked to reproductive disruptions. This study investigated the relationship between PFAS exposure and missed miscarriage in a hospital-based, case-control study in Shanghai, China. There were 393 women in our research, including 198 cases and 195 controls. Concentrations of 30 PFAS in plasma were quantified using HPLC-MS/MS, and 15 PFAS were detected at a rate greater than 90 percent. PFOA, L-PFOS, and PFOS isomers were significantly higher in the cases than those in the controls. 13 PFAS showed significant positive associations with miscarriage risk after adjustment for confounders, particularly PFOA (OR: 2.99, 95 % CI: 1.96–4.68) and various PFOS isomers. BKMR analysis confirmed higher overall PFAS levels were associated with increased miscarriage risk. These findings highlight the potential reproductive toxicity of PFAS and underscore the need for further investigations and regulatory actions to mitigate PFAS exposure in pregnant women.