Microplastics (MPs) have become an emerging threat for organisms. However, the toxicity mechanisms on biota, especially soil biota remain largely unclear. This study distinguished the effects of five types of MPs and their extractable additives on a typical soil oligochaete Enchytraeus crypticus using a traditional ecotoxicological approach combined with gut microbiota analysis. A variety of inorganic and organic compounds were screened in extractable solutions. Both MPs and their extractable additives decreased the growth and survival rates of the worms and shifted the gut microbiota, and the effects were type-specific. The differences between the effects of MPs and their extractable additives on traditional ecotoxicological parameters were insignificant, suggesting that extractable additives were the main toxicity pathways on soil fauna. The type-specific effects of MPs were attributed to the varied chemical compositions of extractable additives, and the compounds responsible for the shift of gut microbiota were further identified. The distinguishable effects on gut microbiota between MPs and their extractable additives together with the significant regressions between gut microbiota and traditional ecotoxicological parameters confirmed that gut microbiota could be a more sensitive indicator of organism's health conditions. Combined, the study provided an important insight into the toxicity mechanisms of MPs on soil fauna and extractable additives of MPs may be a hidden threat.

Atmospheric microplastics have been widely reported in studies around the world. Microfibres are often the dominant morphology found by researchers, although synthetic (i.e., plastic) microfibres are typically just a fraction of the total number of microfibres, with other, non-synthetic, cellulosic microfibres frequently being reported. This study set out to review existing literature to determine the relative proportion of cellulosic and synthetic atmospheric anthropogenic (man-made) microfibres, discuss trends in the microfibre abundances, and outline proposed best-practices for future studies. We conducted a systematic review of the existing literature and identified 33 peer-reviewed articles from Scopus and Google Scholar searches that examined cellulosic microfibres and synthetic microfibres in the atmosphere. Multiple analyses indicate that cellulosic microfibres are considerably more common than synthetic microfibres. FT-IR and Raman spectroscopy data obtained from 24 studies, showed that 57% of microfibres were cellulosic and 23% were synthetic. The remaining were either inorganic, or not determined. In total, 20 studies identified more cellulosic microfibres, compared to 11 studies which identified more synthetic microfibres. The data show that cellulosic microfibres are 2.5 times more abundant between 2016 and 2022, however, the proportion of cellulosic microfibres appear to be decreasing, while synthetic microfibres are increasing. We expect a crossover to happen by 2030, where synthetic microfibres will be dominant in the atmosphere. We propose that future studies on atmospheric anthropogenic microfibres should include information on natural and regenerated cellulosic microfibres, and design studies which are inclusive of cellulosic microfibres during analysis and reporting. This will allow researchers to monitor trends in the composition of atmospheric microfibers and will help address the frequent underestimation of cellulosic microfibre abundance in the atmosphere.

Fe–N co-doped biochar is recently an emerging carbocatalyst for persulfate activation in situ chemical oxidation (ISCO). However, the involved catalytic mechanisms remain controversial and distinct effects of coexisting water components are still not very clear. Herein, we reported a novel N-doped biochar-coupled crystallized Fe phases composite (Fe@N-BC₈₀₀) as efficient and low-cost peroxydisulfate (PDS) activators to degrade bisphenol A (BPA), and the underlying influencing mechanism of coexisting inorganic anions (IA) and humic constituent. Due to the formation of graphitized nanosheets with high defects (AI index>0.5, ID/IG = 1.02), Fe@N-BC₈₀₀ exhibited 2.039, 5.536, 8.646, and 23.154-fold higher PDS catalytic activity than that of Fe@N-BC₆₀₀, Fe@N-BC₄₀₀, N-BC, BC. Unlike radical pathway driven by carbonyl group and pyrrolic N of low/mid-temperature Fe@N–BCs. The defective graphitized nanosheets and Fe-Nx acted separately as electron transfer and radical pathway active sites of Fe@N-BC₈₀₀, where π-π sorption assisted with pyrrolic N and pore-filling facilitated BPA degradation. The strong inhibitory effects of PO₄³⁻ and NO₂⁻ were ascribed to competitive adsorption of phosphate (61.11 mg g⁻¹) and nitrate (23.99 mg g⁻¹) on Fe@N-BC₈₀₀ via electrostatic attraction and hydrogen bonding. In contrast, HA competed for the pyrrolic-N site and hindered electron delivery. Moreover, BPA oxidation pathways initiated by secondary free radicals were proposed. The study facilitates a thorough understanding of the intrinsic properties of designed biochar and contributes new insights into the fate of degradation byproducts formed from ISCO treatment of micropollutants.

Only scarce information is available about the abundance of microplastics (MPs) in Nordic lakes. In this study, the occurrence, types, and distribution of MPs were assessed based on the lake water and sediment samples collected from a sub-basin of Lake Saimaa, Finland. The main goal was to estimate the possible effect of the local wastewater treatment plant (WWTP) on the abundance of MPs in different compartments of the recipient lake area. Collected bottom sediment samples were Cs-137 dated and the chronological structure was utilized to relate the concentrations of MPs to their sedimentation years. Raman microspectroscopy was used for the MPs’ identification from both sample matrices. In addition, MPs consisting of polyethylene (PE), polypropylene (PP) and polystyrene (PS) were quantified from lake water samples by pyrolysis-gas chromatography-mass spectrometry to provide a complementary assessment of MPs based on two different analysis methods, which provide different metrics of the abundance of microplastics. MPs concentrations were highest in sediment samples closest to the discharge site of WWTP effluents (4400 ± 620 n/kg dw) compared to other sites. However, such a trend was not found in lake water samples (0.7 ± 0.1 n/L). Overall, microplastic fibers were relatively more abundant in sediment (70%) than in water (40%), and the majority of detected microplastic fibers were identified as polyester. This indicates that a part of textile fibers passing the WWTP processes accumulate in the sediment close to the discharge site. In addition, the abundance of MPs was revealed to have increased slightly during the last 30 years.

In spring, ozone (O₃) pollution frequently occurrs in eastern China, but key drivers remain uncertain. In this study, interannual variations in springtime ozone in Shanghai, China, from 2013 to 2021, were investigated to assess the health impacts and the effectiveness of recent air pollution control measures. A combination of ground-level measurements of regulated air pollutants, lidar observations, and backward trajectories of air masses was used to identify the key drivers for enhancing springtime O₃. The results show that external imports of O₃ driven by atmospheric circulation are notable sources of springtime surface O₃. For example, the downward transport from the free troposphere could contribute to over 50% of surface O₃ in the morning. The surface O₃ mixing ratios in spring exhibited an upward trend of 0.93 ppb yr⁻¹ (p < 0.05) from 2013 to 2021. The change in meteorological variables, particularly the increase in air temperature, could explain nearly 87% of the springtime O₃ upward trend. The change in anthropogenic emissions of precursors only contributed to a small fraction (<13%) of the increase in springtime O₃. The cumulative exposure of urban residents to O₃ in spring also exhibited a significant upward trend (111 ppb yr⁻¹, p < 0.05). With the rapid increase in surface O₃, premature respiratory mortality attributable to O₃ exposure has fluctuated at approximately 2933 deaths per year since 2016, even though the total deaths from respiratory diseases have significantly declined. Long-term exposure to high O₃ concentrations is a significant contributor to premature respiratory mortality.

Clearfield® wheat (Triticum aestivum) have helped eliminate the toughest grasses and broadleaf weeds in Spain since 2005. This crop production system includes other tolerant cultivars to the application of imidazolinone (IMI) herbicides. However, the continuous use and off-label rates of IMI herbicides can contribute to the development of resistance in Lolium rigidum and other weed species. In this research, the main objectives were to study the resistance mechanisms to acetolactate synthase (ALS) and acetyl coenzyme A carboxylase (ACCase) inhibitors in a L. rigidum accession (LrR) from a Clearfield® wheat field, with a long history rotating these IMI-tolerant crops and compare them with those present in the IMI-tolerant wheat. The resistance to ACCase inhibitors in LrR was due to point mutations (Ile1781Leu plus Asp2078Gly) of the target site gene plus an enhanced herbicide metabolism (EHM), on the other hand, in wheat accessions was due only by EHM. Mechanisms involved in the resistance to ALS inhibitors were both point mutations of the target gene and EHM in the IMI-tolerant wheat, while only evidence of mutation (Trp574Leu) was found in the multiple herbicide resistant L. rigidum accession. This research demonstrates that if crop rotation is not accompanied by the use of alternative sites of action in herbicide-tolerant crops, resistant weeds to herbicide to which crops are tolerant, can easily be selected. Moreover, repeated and inappropriate use of Clearfield® crops and herbicide rotations can lead to the evolution of multiple resistant weeds, as shown in this study, and have also inestimable environmental impacts.

In this study, we backward traced and controlled the pollution of organophosphorus flame retardants (OPFRs) in aquaculture areas from the standpoints of terminal treatment, migration and transformation resistance, and source molecular substitution technology. A regulatory plan to considerably reduce the combined biotoxicity of fish exposed to OPFRs in aquaculture areas and significantly improves the biodegradation of sewage treatment and the efficiency of soil plant-microorganism combined remediation was formulated. Environmentally friendly alternatives of OPFRs were designed. The supplementation scheme of aquatic feed significantly alleviates the toxicity risk of fish exposure to OPFRs in aquafarm (reduced by 121.02%). The regulatory scheme of external stimulus to enhance the biodegradation of OPFRs in wastewater treatment process included an H₂O₂ concentration of 400 mg/L, voltage gradient of 1.5 V/m, and pH of 6.5 can improve the degradation capacity of OPFRs molecules by 88.86%. The degradation of OPFRs can be enhanced by plant-microorganism combined remediation (up to 98.64%) by growing plants whose primary function is phytoextraction in soils dominated by Sphingopyxis sp. and Rhodococcus sp. A 3D-QSAR pharmacophore model based on apoptosis toxicity, mitochondrial dysfunction, oxidative stress response, reproductive, neurotoxicity, gill-inhalation combined toxicity of fish exposed to OPFRs in aquafarm was fabricated. The recommended aquatic feed scheme and the control scheme of enhanced degradation of OPFRs by sewage treatment and soil environment had better applicability for the new-designed OPFRs substitution molecules (the maximum combined toxicity/degradation is reduced/increased by 75.46% and 63.24%, respectively). In this paper, a technical scheme of OPFRs terminal treatment, process regulation, and source control was applied as a cradle-to-grave approach to reduce the ecological toxicity risk of fish exposed to OPFRs in aquaculture areas providing theoretical support for the realization of OPFRs environmental pollution control.

Natural environments have been linked to decreased risk of cardiovascular disease (CVD) and respiratory disease (RSD) mortality. However, few cohort studies have looked at associations of natural environments with CVD or RSD hospitalization. The aim of this study was to evaluate these associations in a cohort of U.S. Medicare beneficiaries (∼63 million individuals). Our open cohort included all fee-for-service Medicare beneficiaries (2000–2016), aged ≥65, living in the contiguous U.S. We assessed zip code-level park cover based on the United States Geological Survey Protected Areas Database, average greenness (Normalized Difference Vegetation Index, NDVI), and percent blue space cover based on Landsat satellite images. Cox-equivalent Poisson models were used to estimate associations of the exposures with first CVD and RSD hospitalization in the full cohort and among those living in urban zip codes (≥1000 persons/mile²). NDVI was weakly negatively correlated with percent park cover (Spearman ρ = −0.23) and not correlated with percent blue space (Spearman ρ = 0.00). After adjustment for potential confounders, percent park cover was not associated with CVD or RSD hospitalization in the full or urban population. An IQR (0.27) increase in NDVI was negatively associated with CVD (HR: 0.97, 95%CI: 0.96, 0.97), but not with RSD hospitalization (HR: 0.99, 95%CI: 0.98, 1.00). In urban zip codes, an IQR increase in NDVI was positively associated with RSD hospitalization (HR: 1.02, 95%CI: 1.00, 1.03). In stratified analyses, percent park cover was negatively associated with CVD and RSD hospitalization for Medicaid eligible individuals and individuals living in low socioeconomic status neighborhoods in the urban population. We observed no associations of percent blue space cover with CVD or RSD hospitalization. This study suggests that natural environments may benefit cardiorespiratory health; however, benefits may be limited to certain contexts and certain health outcomes.

Persulfate-based advanced oxidation process is considered as a promising technology for the degradation of phenol, where efficient, cost effective, and green methods with high peroxydisulfate (PS) activation capacity is of increasing demand. In this work, an in-situ liquid phase precipitation combined with ball milling method was applied for the synthesized of α-FeOOH/biochar, as be the PS activator for phenol degradation. Results showed that the ball-milled α-FeOOH and red pine wood biochar prepared at 700 °C (BM-α-FeOOH/PBC700) exhibited the highest catalytic property with PS for phenol oxidation (a phenol removal rate of 100%), compared with the BM-α-FeOOH (16.0%) and BMPBC700 (66.3%). The presence of intermediate products such as hydroquinone and catechol, and total organic carbon (TOC) removal rate (88.9%) proved the oxidation of phenol in the BM-α-FeOOH/PBC700+PS system. The characterization results showed that the functional groups (e.g., CO, C–O, Fe–O, and Si–O), the dissolved organic matter (DOM) in biochar, the loading of Fe element, and higher degree of graphitization and defect structures, contributed to the activation of PS to form free radicals (i.e., SO₄·⁻, ·OH, ·O₂⁻, and hVB⁺) for phenol oxidation, of which, SO₄·⁻ and ·OH account for 72.1% of the phenol removal rate. The specific contribution to the PS activation for phenol oxidation by each part of the materials was calculated based on the “whole to part” experiment. The contribution of DOM, acid-soluble substance, and carbon matrix and basal part in BM-α-FeOOH/PBC700 were 6.0%, 40.9%, and 53.1%, respectively. The reusability experiments of BM-α-FeOOH/PBC700 demonstrated that the composite was relatively stable after four cycles of reuse. Among three co-existing anions (NO₃⁻, Cl⁻, and HCO₃⁻), HCO₃⁻ played the most significant inhibition effects on phenol removal through reducing the phenol removal rate from 89.6% to 77.9%. This work provides guidance for the design of high active and stable carbon materials that activate PS to remove phenol.

An increasing body of evidence has linked greenspace and various health outcomes in children and adolescents, but the conclusions were inconsistent. For this review, we comprehensively summarized the measurement methods of greenspace, resultant health outcomes, and potential mechanisms from epidemiological studies in children and adolescents (aged ≤19 years). We searched for studies published and indexed in MEDLINE and EMBASE (via Ovid) up to April 11, 2022. There were a total of 9,291 studies identified with 140 articles from 28 countries finally assessed and included in this systematic review. Over 70% of the studies were conducted in highly urbanised countries/regions, but very limited research has been done in low-and middle-income countries and none in Africa. Measures of greenspace varied. Various health outcomes were reported, including protective effects of greenspace exposure on aspects of obesity/overweight, myopia, lung health, circulatory health, cognitive function, and general health in children and adolescents. The associations between greenspace exposure and other health outcomes were inconsistent, especially for respiratory health studies. We pooled odds ratios (OR) using random-effects meta-analysis for health outcomes of asthma (OR = 0.94, 95%CI: 0.84 to 1.06), allergic rhinitis (OR = 0.95; 95% CI: 0.73 to 1.25), and obesity/overweight (OR = 0.91, 95%CI: 0.84 to 0.98) with per 0.1 unit increase in normalized difference in vegetation index (NDVI). These associations have important implications for the assessment and management of urban environment and health in children and adolescents.