Search Results (223)

Wastewater treatment plants (WWTPs) function as engineered ecosystems in which microbial consortia mediate nutrient cycling, xenobiotic degradation, and heavy metal detoxification. This review discusses a forward-looking roadmap that integrates microbial ecology, multi-omics diagnostics, and artificial intelligence (AI) for next-generation treatments. Meta-analyses suggest that a globally conserved core microbiome indicates sludge functions, with high predictive value for treatment stability. Multi-omics approaches, including metagenomics, metatranscriptomics, and environmental DNA (eDNA) profiling, have integrated microbial composition with greenhouse gas (GHG) emissions, showing that WWTPs contribute 2–5% of anthropogenic nitrous oxide (N₂O) emissions. Emerging AI-enhanced eDNA models have achieved >90% predictive accuracy for effluent quality and antibiotic resistance gene (ARG) prevalence, facilitating near-real-time monitoring and adaptive control of effluent quality. Key advances include microbial strategies for degrading organic pollutants, pesticides, and heavy metals and monitoring industrial effluents. This review highlights both translational opportunities, including engineered microbial consortia, AI-driven digital twins and molecular indices, and persistent barriers, including ARG dissemination, resilience under environmental stress and regulatory integration. Future WWTPs are envisioned as adaptive, climate-conscious biorefineries that recover resources, mitigate ecological risks, and reduce their carbon footprint. Full article

Currently, ozone (O₃) has become one of the primary air pollutants in China, underscoring the importance of analyzing ozone formation sensitivity (OFS) for effective pollution control. Ozone sensitivity indices serve as effective tools for OFS identification. Among them, the ratio of volatile organic compounds (VOCs) to nitrogen oxides (NO_x)—such as the formaldehyde-to-nitrogen dioxide ratio (FNR, defined as HCHO/NO₂, where HCHO represents VOCs and NO₂ represents NO_x)—is one of the most widely used satellite-based indicators. Recent studies have highlighted glyoxal (CHOCHO) as another critical ozone precursor, prompting the proposal of the glyoxal-to-nitrogen dioxide ratio (GNR, CHOCHO/NO₂) as an alternative metric. This study systematically compares the performance of FNR and GNR across four major urban agglomerations in China: Beijing–Tianjin–Hebei (BTH), the Yangtze River Delta (YRD), the Pearl River Delta (PRD), and the Chengdu–Chongqing (CY) region, by integrating satellite remote sensing with ground-based observations. Results reveal that both indices exhibit consistent spatial trends in OFS distribution, transitioning from VOC-limited regimes in urban centers to NO_x-limited regimes in surrounding suburban areas. However, differences emerge in threshold values and classification outcomes. During summer, FNR identifies urban areas as transitional regimes (or VOC-limited in regions such as YRD and PRD), while suburban areas are classified as NO_x-limited. In contrast, GNR, which shows heightened sensitive to anthropogenic VOCs (AVOCs), exhibits a more restricted spatial extent in the transition regimes. By autumn, most urban areas shift toward VOC-limited regimes, while suburban regions remain NO_x-limited. Thresholds for both VOCs and NO_x increase during this period, with GNR demonstrating stronger sensitivity to NO_x. These findings underscore that the choice between FNR and GNR directly influences OFS determination, as their differing responses to biogenic and anthropogenic emissions lead to different conclusions. Future research should focus on integrating the complementary strengths of both indices to develop a more robust OFS identification method, thereby providing a theoretical basis for formulating effective ozone control strategies. Full article

Xiamen, a rapidly developing coastal metropolis and tourist hub in southeastern China, faces air quality challenges due to its dense population and tourism reliance. This study investigates PM_2.5 sources and temporal variations during autumn 2013–2017 via chemical characterization, mass reconstruction, and receptor modeling. The Positive Matrix Factorization (PMF) model identified five sources: secondary sulfate (31%), coal/vehicle emissions (28%), industrial emissions with secondary organic aerosols (SOA, 20%), ship emissions (14%), and fugitive dust (7%). Interannual variations in source contributions highlighted impacts of anthropogenic activities, meteorology, power plant upgrades, and stricter vehicle standards. PM_2.5 declined 19% (2013–2017), driven by emission controls, while SOA surged 42% (2015–2017) due to VOC oxidation and lower temperatures. Backward trajectory and Potential Source Contribution Function (PSCF) analyses revealed significant regional transport from northern industrial zones (32% contribution) and maritime activities. Ship emissions, which have remained relatively stable over the years, underscore the need for stricter marine regulations. Fugitive dust peaked in 2015 (25.8% of PM_2.5), linked to urban construction. The findings emphasize the interplay of local emissions and regional transport in shaping PM_2.5 pollution, providing a scientific basis for targeted control strategies in coastal cities with similar socioeconomic and geographic contexts. Full article

Geopolymers represent an innovative and environmentally sustainable alternative to traditional construction materials, offering significant potential for reducing anthropogenic CO₂ emissions. Among these, phosphoric acid-activated metakaolin-based systems have attracted increasing attention for their chemical and thermal resilience. In this study, we present a comprehensive structural and mechanical evaluation of metakaolin-based geopolymers synthesized across a wide range of Al/P molar ratios (0.8–4.0). Six formulations were systematically prepared and analyzed using X-ray powder diffraction (XRPD), small-angle X-ray scattering (SAXS), Fourier-transform infrared spectroscopy (FTIR), solid-state nuclear magnetic resonance (ssNMR), and complementary mechanical testing. The novelty of this work lies in the integrated mapping of composition–structure–property relationships across the broad Al/P spectrum under controlled synthesis, combined with the rare application of SAXS to reveal composition-dependent nanoscale domains (~18–50 nm). We identify a stoichiometric window at Al/P ≈ 1.5, where complete acid consumption leads to a structurally homogeneous AlVI–O–P network, yielding the highest compressive strength. In contrast, acid-rich systems exhibit divergent flexural and compressive behaviors, with enhanced flexural strength linked to hydrated silica domains arising from metakaolin dealumination, quantitatively tracked by ²⁹Si MAS NMR. XRPD further reveals the formation of uncommon Si–P crystalline phases (SiP₂O₇, Si₅P₆O₂₅) under low-temperature curing in acid-rich compositions. Together, these findings provide new insights into the nanoscale structuring, phase evolution, and stoichiometric control of silica–alumino–phosphate geopolymers, highlighting strategies for optimizing their performance in demanding thermal and chemical environments. Full article

Ozone pollution in densely populated urban regions poses a great threat to public health, due to the intensive anthropogenic emissions of ozone precursors and is further aggravated by global warming and the urban heat island phenomenon. Air quality models have been utilized to formulate and evaluate air pollution control strategies. This study presents a comprehensive modeling assessment of ozone mitigation strategies during an ozone pollution episode in Changzhou, an industrial city in the Yangtze River Delta region. Utilizing the Community Multiscale Air Quality Modeling System (CMAQ), we quantified the contribution of ozone from different emission sectors and counties within Changzhou using the integrated source apportionment method (ISAM). During the pollution period, local emissions within Changzhou account for an average of 41.5% of MDA8 ozone, with particularly notable contributions from Jingkai (11.2%), Wujin (9.5%), and Liyang (7.8%). Upon these findings, we evaluated three sets of emission reduction scenarios: uniform, sector-specific, and county-specific reductions. Results show that industry and transportation are responsible for over 20% of ozone concentrations, and targeted reductions in these sources yielded the most significant decreases in ozone levels. Notably, reducing industrial emissions alone decreased ozone concentrations by 3.2 μg m⁻³ during the pollution episode. County-specific reductions revealed the importance of targeted strategies, with certain counties showing more pronounced responses to emission controls. On a daily basis, emission reductions in Xinbei contributed to a maximum ozone decrease of 4.4 μg m⁻³. This study provides valuable insights into the efficacy of different mitigation measures in Changzhou and offers a practical and useful framework for policymakers to implement strategies while addressing the complexities of urban air quality management. Full article

Promoting sustainable development requires a clear understanding of how short-term fluctuations in anthropogenic emissions affect urban environmental quality. This is especially relevant for cities experiencing rapid industrial changes or emergency policy interventions. Among key environmental concerns, variations in ambient pollutants like ozone (O₃) are closely tied to both public health and long-term sustainability goals. However, traditional chemical transport models often face challenges in accurately estimating emission changes and providing timely assessments. In contrast, statistical approaches such as the difference-in-differences (DID) model utilize observational data to improve evaluation accuracy and efficiency. This study leverages the synthetic difference-in-differences (SDID) approach, which integrates the strengths of both DID and the synthetic control method (SCM), to provide a more reliable and accurate analysis of the impacts of interventions on city-level air quality. Using Shanghai’s 2022 lockdown as a case study, we compare the deweathered ozone (O₃) concentration in Shanghai to a counterfactual constructed from a weighted average of cities in the Yangtze River Delta (YRD) that did not undergo lockdown. The quasi-natural experiment reveals an average increase of 4.4 μg/m³ (95% CI: 0.24–8.56) in Shanghai’s maximum daily 8 h O₃ concentration attributable to the lockdown. The SDID method reduces reliance on the parallel trends assumption and improves the estimate stability through unit- and time-specific weights. Multiple robustness checks confirm the reliability of these findings, underscoring the efficacy of the SDID approach in quantitatively evaluating the causal impact of emission perturbations on air quality. This study provides credible causal evidence of the environmental impact of short-term policy interventions, highlighting the utility of SDID in informing adaptive air quality management. The findings support the development of timely, evidence-based strategies for sustainable urban governance and environmental policy design. Full article

Volatile organic compounds (VOCs) are highly volatile chemicals in natural and anthropogenic environments, significantly affecting indoor air quality. Major sources of indoor VOCs include emissions from building materials, furnishings, and consumer products. Natural wood products release VOCs, including terpenes and aldehydes, which exert diverse health effects ranging from mild respiratory irritation to severe outcomes, such as formaldehyde-induced carcinogenicity. The temporal dynamics of VOC emissions were investigated, and the toxicological and physiological effects of the VOCs emitted by two types of natural wood, Korean Red Pine (Pinus densiflora) and Japanese Cypress (Chamaecyparis obtusa), were evaluated. Using female C57BL/6 mice as an animal model, the exposure setups included phytoncides, formaldehyde, and intact wood samples over short- and long-term durations. The exposure effects were assessed using oxidative stress markers, antioxidant enzyme activity, hepatic and renal biomarkers, and inflammatory cytokine profiles. Long-term exposure to Korean Red Pine and Japanese Cypress wood VOCs did not induce significant pathological changes. Japanese Cypress exhibited more distinct benefits, including enhanced oxidative stress mitigation, reduced systemic toxicity, and lower pro-inflammatory cytokine levels compared to the negative control group, attributable to its more favorable VOC emission profile. These findings highlight the potential health and environmental benefits of natural wood VOCs and offer valuable insights for optimizing timber use, improving indoor air quality, and informing public health policies. Full article

Long-term source apportionment of PM_2.5 during high-pollution periods is essential for achieving sustained reductions in both PM_2.5 levels and their health impacts. This study conducted PM_2.5 sampling in Shenzhen from January to March over the years 2021–2024 to investigate the long-term impact of coronavirus disease 2019 and the short-term impact of the Spring Festival on PM_2.5 levels. The measured average PM_2.5 concentration during the research period was 22.5 μg/m³, with organic matter (OM) being the dominant component. Vehicle emissions, secondary sulfate, secondary nitrate, and secondary organic aerosol were identified by receptor model as the primary sources of PM_2.5 during the observational periods. The pandemic led to a decrease of between 30% and 50% in the contributions of most anthropogenic sources in 2022 compared to 2021, followed by a rebound. PM_2.5 levels in January–March 2024 dropped by 1.4 μg/m³ compared to 2021, mainly due to reduced vehicle emissions, secondary sulfate, fugitive dust, biomass burning, and industrial emissions, reflecting Shenzhen’s and nearby cities’ effective control measures. However, secondary nitrate and fireworks-related emissions rose significantly. During the Spring Festival, PM_2.5 concentrations were 23% lower than before the festival, but the contributions of fireworks burning exhibited a marked increase in both 2023 and 2024. Specifically, during intense peak events, fireworks burning triggered sharp, short-term spikes in characteristic metal concentrations, accounting for over 50% of PM_2.5 on those peak days. In the future, strict control over vehicle emissions and enhanced management of fireworks burning during special periods like the Spring Festival are necessary to reduce PM_2.5 concentration and improve air quality. Full article

The increasing levels of ozone pollution have become a significant environmental issue in urban areas worldwide. Previous studies have confirmed that the urban ozone pollution in China is mainly controlled by volatile organic compounds (VOCs) rather than nitrogen oxides. Therefore, a study on the emission characteristics and source analysis of VOCs is important for controlling urban ozone pollution. In this study, hourly concentrations of 57 VOC species in four groups were obtained in April 2022, a period of high ozone pollution in Kunming, China. The ozone formation potential analysis showed that the accumulated reactive VOCs significantly contributed to the subsequent ozone formation, particularly aromatics (44.16%) and alkanes (32.46%). In addition, the ozone production rate in Kunming is mainly controlled by VOCs based on the results of the empirical kinetic modeling approach (K_NOx/K_VOCs = 0.25). The hybrid single-particle Lagrangian integrated trajectory model and polar coordinate diagram showed high VOC and ozone concentrations from the southwest outside the province (50.28%) and the south in local areas (12.78%). Six factors were obtained from the positive matrix factorization model: vehicle exhaust (31.80%), liquefied petroleum gas usage (24.16%), the petrochemical industry (17.81%), fuel evaporation (11.79%), coal burning (7.47%), and solvent usage (6.97%). These findings underscore that reducing anthropogenic VOC emissions and strengthening controls on the related sources could provide a scientifically robust strategy for mitigating ozone pollution in Kunming. Full article

Ozone (O₃) and fine particulate matter (PM_2.5) are critical atmospheric pollutants whose complex chemical coupling presents significant challenges for multi-pollutant control strategies. This study investigated the spatiotemporal variations and driving mechanisms of O₃ and PM_2.5 in Jiaxing, China, during different COVID-19 lockdown periods from November 2019 to January 2024. Using high-resolution monitoring data, random forest modeling, and HYSPLIT backward trajectory analysis, we quantified the relative contributions of anthropogenic emissions, meteorological conditions, and regional transport to the formation and variation of O₃ and PM_2.5 concentrations. The results revealed a distinct inverse relationship between O₃ and PM_2.5, with meteorologically normalized PM_2.5 decreasing significantly (−5.0 μg/m³ compared to the pre-lockdown baseline of 0.6 μg/m³), while O₃ increased substantially (15.2 μg/m³ compared to the baseline of 5.3 μg/m³). Partial dependency analysis revealed that PM_2.5-O₃ relationships evolved from linear to non-linear patterns across lockdown periods, while NO₂-O₃ interactions indicated shifts from VOC-limited to NO_x-limited regimes. Regional transport patterns exhibited significant temporal variations, with source regions shifting from predominantly northern areas pre-lockdown to more diverse directional contributions afterward. Notably, the partial lockdown period demonstrated the most balanced pollution control outcomes, maintaining reduced PM_2.5 levels while avoiding O₃ increases. These findings provide critical insights for developing targeted multi-pollutant control strategies in the Yangtze River Delta region and similar urban environments. Full article

Since pre-industrial times, anthropogenic methane emissions have increased and are partly responsible for a changing global climate. Natural gas and oil extraction activities are one significant source of anthropogenic methane. While methods have been developed and refined to quantify onshore methane emissions, the ability of methods to directly quantify emissions from offshore production facilities remains largely unknown. Here, we review recent studies that have directly measured emissions from offshore production facilities and critically evaluate the suitability of these measurement strategies for emission quantification in a marine environment. The average methane emissions from production platforms measured using downwind dispersion methods were 32 kg h⁻¹ from 188 platforms; 118 kg h⁻¹ from 104 platforms using mass balance methods; 284 kg h⁻¹ from 151 platforms using aircraft remote sensing; and 19,088 kg h⁻¹ from 10 platforms using satellite remote sensing. Upon review of the methods, we suggest the unusually large emissions, or zero emissions observed could be caused by the effects of a decoupling of the marine boundary layer (MBL). Decoupling can happen when the MBL becomes too deep or when there is cloud cover and results in a stratified MBL with air layers of different depths moving at different speeds. Decoupling could cause: some aircraft remote sensing observations to be biased high (lower wind speed at the height of the plume); the mass balance measurements to be biased high (narrow plume being extrapolated too far vertically) or low (transects miss the plume); and the downwind dispersion measurements much lower than the other methods or zero (plume lofting in a decoupled section of the boundary layer). To date, there has been little research on the marine boundary layer, and guidance on when decoupling happens is not currently available. We suggest an offshore controlled release program could provide a better understanding of these results by explaining how and when stratification happens in the MBL and how this affects quantification methodologies. Full article

Polycyclic aromatic hydrocarbons (PAHs) and their substituted derivatives (SPAHs) are persistent organic pollutants derived from incomplete combustion of fossil fuels and industrial processes. These compounds are of global concern due to their carcinogenicity and environmental persistence. This study provides the first comprehensive analysis of PAH and SPAH contamination in Suzhou’s rapidly urbanizing watersheds, integrating ultra-high-performance liquid chromatography and high-resolution mass spectrometry with multidimensional risk assessment to address critical gaps in understanding pollutant dynamics in urban aquatic systems. Key findings reveal that SPAHs were significantly more abundant than parent PAHs (mean ∑19 SPAHs = 107.43 ng/L vs. ∑8 PAHs = 48.05 ng/L), with hydroxylated derivatives accounting for 67.9% of the total SPAHs, indicating active environmental transformation processes. Source apportionment identified coal combustion and industrial emissions as the dominant contributors (58.2% of PAHs), directly linking contamination patterns to localized anthropogenic activities. Notably, industrial zones exhibited unexpected toxicity hotspots, where SPAH toxicity equivalents (e.g., 3-OH-BaP) surpassed parent PAHs 2–5-fold, demonstrating substituent-driven toxicity enhancement—a critical finding for regulatory prioritization. This study advances the field by uncovering SPAHs as emerging risks in urban waterways, challenging traditional PAH-centric monitoring frameworks, and providing a novel integration of analytical chemistry and spatial risk mapping to guide targeted pollution control (e.g., prioritizing industrial discharges and non-exhaust traffic emissions). Furthermore, it highlights the urgent need for updated toxicological databases to account for substituted PAH derivatives and advocates for the regulatory inclusion of SPAHs. These insights underscore the necessity of adapting environmental policies to address complex pollutant mixtures in rapidly developing regions, emphasizing the replicability of the proposed framework for urban watershed management. Full article

Understanding pollution levels, ecological health risks, and sources of potentially toxic metals (PTMs) in the soil from university campuses is critical for assessing environmental safety. Soil samples were collected from 12 locations across urban parks and green areas at Sohag University in Egypt. The samples were processed and analysed for heavy metals, including iron (Fe), manganese (Mn), cobalt (Co), nickel (Ni), chromium (Cr), lead (Pb), zinc (Zn), copper (Cu), and cadmium (Cd). Pollution levels were evaluated using indices such as the pollution index (PI), pollution load index (PLI), geo-accumulation index (I_geo), and enrichment factors (EFs). Among the pollution indices, the EFs showed the highest sensitivity in detecting anthropogenic contributions, particularly for Cd, Pb, and Cr. Spatial distribution maps and multivariate statistical analyses, including correlation matrix (CM), principal component analysis (PCA), and cluster analysis (CA), were applied to identify the relationships between PTMs and soil properties, and source apportionment was performed using positive matrix factorisation (PMF). The results indicated that Mn, Ni, and Co were primarily geogenic, whereas Pb, Zn, Cr, and Cd showed higher concentrations, suggesting moderate-to-significant anthropogenic pollution. Pb and Cd pose considerable ecological risks, whereas other metals such as Cr and Cu exhibit moderate ecological threats. The non-carcinogenic and carcinogenic risks to the students were within safe limits, as defined by United States Environmental Protection Agency (USEPA) threshold values. Source apportionment using PMF identified five main sources of PTMs: industrial and anthropogenic activities (30.0%), traffic emissions (25.0%), natural soil processes (20.0%), agricultural practices (15.0%), and mixed industrial traffic sources (10.0%). These findings emphasise the importance of controlling anthropogenic activities to ensure a safer campus environment. Full article

Biogenic volatile organic compounds (BVOCs) emitted by plants contribute to secondary air pollution through photochemical reactions in sunlight. Due to the influence of multiple factors, accurately characterizing and quantifying the emission of BVOCs from plant sources is challenging, which poses significant obstacles to the effective management and control of BVOCs. Therefore, this paper summarizes the emission mechanisms of BVOCs from plants, explores the primary factors influencing variations in the emission rates of these compounds, and evaluates the advantages and limitations of contemporary “measurement-modeling” methods for characterizing BVOC emissions. It is concluded that current measurement techniques still need to be further developed to meet the criteria of simplicity, affordability, and high precision simultaneously, and in terms of modeling and prediction studies, there is a lack of in-depth research on the atmospheric chemistry of BVOCs and the synergistic effects of multiple factors. Finally, it is suggested to leverage interdisciplinary strengths to develop advanced measurement technologies and high-resolution models for monitoring volatile compounds. Additionally, strategically selecting low-BVOC tree species in pollution-vulnerable urban areas—contingent on rigorous ecological assessments—combined with stringent controls on anthropogenic precursors (e.g., anthropogenic volatile organic compounds (AVOCs)) could serve as a complementary measure to mitigate secondary pollution. Full article

Trees mediate critical biogeochemical cycles involving nutrients, pollutants, water, and energy at the interface between terrestrial biosphere and atmosphere. Forest ecosystems significantly influence the global cycling of mercury (Hg), serving as important sinks and potential sources of re-emission through various biotic and abiotic processes. Anthropogenic Hg emissions, predominantly from industrial activities, mining, and fossil fuel combustion, have substantially altered the natural Hg cycle, intensifying ecotoxicological concerns and establishing forests as primary routes for atmospheric Hg deposition into terrestrial reservoirs. This perturbation profoundly affects global atmospheric Hg concentrations, residence times, and spatial distribution patterns. While early investigations focused on forest stands near heavily polluted areas, contemporary research has expanded to diverse ecosystems, revealing that trees provide tissues that function as temporal archives for atmospheric-terrestrial Hg exchange. Leaves capture high-resolution records of contemporary Hg dynamics at sub-annual timescales, whereas annual growth rings preserve multi-decadal chronologies of historical atmospheric exposure. Incorporating this dual temporal perspective is crucial for analysing Hg deposition trends and assessing the efficacy of environmental policies designed to control and mitigate Hg pollution. This review critically evaluates recent developments concerning the ecophysiological determinants of Hg accumulation in trees, highlighting how combined foliar and dendrochemical analytical methods strengthen our mechanistic understanding of vegetation-atmosphere Hg exchange. To enhance biomonitoring approaches, we emphasised the need for methodological standardisation, deeper integration of ecophysiological variables, and consideration of climate change implications as priority research areas. Furthermore, integrating Hg measurements with functional markers (δ¹³C and δ¹⁸O) and Hg isotope analyses strengthens the capacity to differentiate between physiological and environmental influences on Hg accumulation, thereby refining the mechanistic framework underlying effective tree-based Hg biomonitoring. Full article