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The aqueous film formed on aerosol surfaces enhances the absorption of urban locally emitted free amino acids during the dust event 在尘埃事件中,气溶胶表面形成的水膜增强了对城市局部释放的游离氨基酸的吸收
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2026-01-01 DOI: 10.1016/j.aeaoa.2025.100407
NengJian Zheng , Ren-Guo Zhu , Meiju Yin , Yaping Li , Yujun Ma , Yuanyuan Zhu , LingShuang Deng , Hao Xiao , Yichen Zou , Hua-Yun Xiao
Free amino acids (FAAs) are essential bioavailable organic nitrogen compounds, yet their atmospheric concentrations, distributions, sources, and secondary formation processes during dust events remain poorly understood. Here, we investigated FAA concentrations, molecular distributions, and δ15N signatures in PM2.5 collected from four cities in the Beijing-Tianjin-Hebei air pollution transport channel during spring 2018 to investigate the impact of a dust event on the concentrations, sources and formation mechanism of FAAs in PM2.5. During the dust event, total FAA (TFAA) concentrations across all sites were substantially higher than those environments not influenced by the dust events and exhibited a strong linear correlation with PM10 (r = 0.6, p < 0.01), indicating that dust events significantly enhance FAA levels. We observed regional variability in the average TFAA concentration during the dust event. The concentrations in Beijing, Tianjin, Shijiazhuang and Taiyuan increased by factors of 1.05, 1.36, 1.55 and 1.63, respectively. Among these four sites, Taiyuan exhibited the most pronounced increase, with its TFAA concentration rising from 0.24 ± 0.07 μg m−3 during the non-dust period to 0.39 ± 0.003 μg m−3 during the dust event (p < 0.05). These regional differences underscore the influence of local sources and atmospheric quality parameters. The consistent FAA composition profiles and δ15N values of TFAA and glycine between dust and non-dust periods across all sites further supported that local sources, rather than long-range transport from the Gobi Desert, was the major contributor to atmospheric FAA pool even during the dust event. In Taiyuan, temporal variations of aerosol liquid water (ALW) were highly correlated with total and subgrouped FAAs (r > 0.8, p < 0.01), identifying ALW as a key factor controlling FAA concentrations. It suggested that even under the low relative humidity conditions of dust events, hygroscopic aerosol growth can facilitate the partitioning of FAAs into the particle phase, leading to higher observed FAA concentrations. Our findings provide new insights into the impact of dust events on FAAs in polluted urban environments and provide a basis for assessing the ecological effects of atmospheric dust transport.
游离氨基酸(FAAs)是重要的生物可利用有机氮化合物,但其在大气中的浓度、分布、来源和在粉尘事件中的二次形成过程尚不清楚。通过对2018年春季京津冀4个城市PM2.5中FAA浓度、分子分布和δ15N特征的研究,探讨一次沙尘事件对PM2.5中FAA浓度、来源和形成机制的影响。在沙尘事件期间,所有站点的总FAA (TFAA)浓度均显著高于未受沙尘事件影响的环境,且与PM10呈强线性相关(r = 0.6, p < 0.01),表明沙尘事件显著提高了FAA水平。我们观察到沙尘事件期间平均TFAA浓度的区域差异。北京、天津、石家庄和太原的浓度分别增加了1.05、1.36、1.55和1.63倍。其中,太原的TFAA浓度上升最为显著,从无尘期的0.24±0.07 μ m−3上升到有尘期的0.39±0.003 μ m−3 (p < 0.05)。这些区域差异强调了局地源和大气质量参数的影响。在沙尘期和非沙尘期,所有站点的FAA组成剖面和TFAA和甘氨酸的δ15N值一致,进一步支持了局地源而非戈壁沙漠的远距离输送是沙尘期间大气FAA库的主要贡献者。太原市气溶胶液态水(ALW)的时间变化与总FAAs和亚分组FAAs高度相关(r > 0.8, p < 0.01),表明ALW是控制FAA浓度的关键因素。这表明,即使在低相对湿度的沙尘条件下,吸湿性气溶胶的生长也能促进FAAs进入颗粒相,从而导致较高的观测到的FAA浓度。研究结果为研究城市污染环境中沙尘事件对FAAs的影响提供了新的思路,并为评估大气沙尘运输的生态效应提供了依据。
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引用次数: 0
An update of emission factors for nitric oxide emissions from croplands and grasslands 农田和草地一氧化氮排放因子的更新
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2026-01-01 DOI: 10.1016/j.aeaoa.2025.100410
Gokul Prasad Mathivanan , Andreas Gattinger , Roland Fuß
Nitric Oxide (NO), an intermediate product in the soil nitrogen cycle, is also an air pollutant causing adverse health effects, including contribution towards the formation of fine particulate matter and tropospheric ozone. Accurate quantification of NO emissions is necessary to mitigate these impacts, but current emission factors used in national greenhouse gas and air pollutant inventories are associated with substantial uncertainty, necessitating an updated assessment based on recent field measurements. In this study, we compiled a comprehensive dataset of 692 field observations of NO measurements from 128 studies conducted globally. Using Bayesian generalised linear mixed-effects models, we derived new emission factors that account for synthetic and organic fertiliser inputs, climate zones and crop groups. The new global emission factor (expressed as mass fraction of nitrogen) for synthetic nitrogen inputs to common crops and grasslands was 0.0042 kg NO-N (kg N)−1 (95 % credible interval: 0.0035–0.0049), while organic nitrogen inputs exhibited a negligible fertiliser induced emission factor of 0.0001 kg NO-N (kg N)−1 (95 % CI: 0.0003 – 0.0005). The emission factors varied markedly upon stratification by climate zones and crop groups, with higher emission factors from synthetic fertilisers in the tropical rainforest regions, while paddy rice cultivation exhibited negligible fertiliser-induced NO emissions and tea plantations showed exceptionally high emissions with a factor of 0.0155 kg NO-N (kg N)−1 (95 % CI: 0.0101–0.0225). The new emission factors are considerably lower than the Tier 1 value of 0.0133 (0.0015–0.0317) kg NO-N (kg N)−1), currently recommended in the EMEP/EEA guidelines. Application to nitrogen fertiliser input data from EU member states' 2025 Informative Inventory Reports indicates that, adopting the new emission factors would result in reported emissions from synthetic fertilisers being lower by approximately 65 %. These findings highlight the need for refined inventory methodologies, replacing the default emission factor with climate and crop specific values, to better inform strategies for nitrogen management and air quality monitoring.
一氧化氮(NO)是土壤氮循环中的中间产物,也是一种空气污染物,对健康造成不利影响,包括促进细颗粒物和对流层臭氧的形成。为了减轻这些影响,有必要对NO排放进行准确的量化,但目前在国家温室气体和空气污染物清单中使用的排放因子具有很大的不确定性,因此需要根据最近的实地测量进行更新评估。在这项研究中,我们编制了来自全球128项研究的692次NO测量的综合数据集。利用贝叶斯广义线性混合效应模型,我们得出了新的排放因子,考虑了合成和有机肥料的投入、气候带和作物群。普通作物和草地合成氮输入的新的全球排放因子(以氮的质量分数表示)为0.0042 kg NO-N (kg N)−1(95%可信区间:0.0035-0.0049),而有机氮输入的肥料诱导排放因子为0.0001 kg NO-N (kg N)−1(95%可信区间:0.0003 - 0.0005),可以忽略不计。不同气候区和作物组的排放因子差异显著,热带雨林地区合成肥料的排放因子较高,而水稻种植的排放因子可以忽略不计,茶园的排放因子异常高,为0.0155 kg NO-N (kg N)−1 (95% CI: 0.0101 ~ 0.0225)。新的排放系数远低于一级值0.0133 (0.0015-0.0317)kg NO-N (kg N)−1),目前在EMEP/EEA指南中推荐。对欧盟成员国2025年信息清单报告中的氮肥投入数据的应用表明,采用新的排放因子将导致合成肥料的报告排放量降低约65%。这些发现强调需要改进清单方法,用气候和作物特定值取代默认排放因子,以便更好地为氮管理和空气质量监测战略提供信息。
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引用次数: 0
Multilinear regression analysis of PM2.5 in Kampala and Fort Portal cities: Effects of meteorological factors and lagged pollution 坎帕拉和福特Portal城市PM2.5的多元线性回归分析:气象因素和滞后污染的影响
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2026-01-01 DOI: 10.1016/j.aeaoa.2025.100411
Fidel Raja Wabinyai , Richard Sserunjogi , Gideon Lubisia , Deo Okure , Edwin Akugizibwe , Jennifer Kutesakwe , Angela Nshimye , Alex Ndyabakira , Engineer Bainomugisha
Rapid urbanization across Sub-Saharan Africa intensifies fine particulate matter (PM2.5) pollution, yet the combined effects of meteorology and pollution persistence remain poorly understood. This study investigates the spatiotemporal variability of PM2.5 in Kampala (urban) and Fort Portal (semi-urban), Uganda, using daily observations from October 2021 to January 2024. Calibrated low-cost AirQo sensor data were integrated with meteorological parameters, including temperature, humidity, wind speed, wind direction, and precipitation, as well as one-day lagged PM2.5, to develop enhanced multilinear regression (MLR) models. Results revealed strong seasonal contrasts, with mean dry-season concentrations in Kampala (38.3 μgm−3) and Fort Portal (32.9 μgm−3) exceeding World Health Organization and NEMA-Uganda limits. Model performance varied by city, explaining up to 57 % of daily PM2.5 variability in Kampala and 80 % in Fort Portal. The inclusion of lagged PM2.5 significantly improved model accuracy, highlighting persistence effects under stagnant meteorological conditions. Wind rose analysis showed that southerly and westerly winds enhanced pollutant transport, particularly during dry months, suggesting potential transboundary contributions to Fort Portal's pollution burden. Although the models performed well during dry seasons, predictive power declined in wet seasons due to rainfall-induced washout effects not fully captured by linear formulations. These findings emphasize the importance of meteorological drivers and pollution persistence in shaping urban air quality and support data-driven interventions such as emission control, traffic management, biomass burning reduction, and regional cooperation to protect public health in rapidly urbanizing African cities.
撒哈拉以南非洲地区的快速城市化加剧了细颗粒物(PM2.5)污染,但人们对气象和污染持续性的综合影响仍知之甚少。利用2021年10月至2024年1月的日观测资料,研究了乌干达坎帕拉(城市)和波特尔堡(半城市)PM2.5的时空变化。校准后的低成本AirQo传感器数据与气象参数(包括温度、湿度、风速、风向、降水以及滞后一天的PM2.5)相结合,建立增强的多元线性回归(MLR)模型。结果显示出强烈的季节差异,坎帕拉(38.3 μgm−3)和波特尔堡(32.9 μgm−3)的旱季平均浓度超过了世界卫生组织和nema -乌干达标准。模型的性能因城市而异,坎帕拉和波尔特堡的PM2.5日变化可分别解释57%和80%。纳入滞后PM2.5显著提高了模型精度,突出了停滞气象条件下的持续效应。风玫瑰分析表明,南风和西风加强了污染物的运输,特别是在干旱月份,这表明可能对波特尔堡的污染负担有跨界贡献。尽管模型在旱季表现良好,但由于降雨引起的冲刷效应未被线性公式完全捕获,因此在雨季预测能力下降。这些研究结果强调了气象驱动因素和污染持续性在塑造城市空气质量方面的重要性,并支持数据驱动的干预措施,如排放控制、交通管理、减少生物质燃烧和区域合作,以保护快速城市化的非洲城市的公众健康。
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引用次数: 0
Assessment of contributors to airborne PAHs and heavy metals in PM10 using temporal, spatial, traffic and heating data in explainable machine learning models 在可解释的机器学习模型中使用时间、空间、交通和供暖数据评估PM10中空气中多环芳烃和重金属的贡献者
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2026-01-01 DOI: 10.1016/j.aeaoa.2026.100413
Nikolina Račić , Stanko Ružičić , Valentino Petrić , Teo Terzić , Mario Antunović , Ivan Škaro , Gordana Pehnec , Ivan Bešlić , Ivana Jakovljević , Zdravka Sever Štrukil , Jasmina Rinkovec , Silva Žužul , Mario Lovrić
Air pollution in urban areas originates from multiple interacting sources and is strongly influenced by meteorology, yet direct emission data are often incomplete. This study quantifies how meteorological conditions, station location, and proxy indicators of traffic and residential heating affect PM10-bound polycyclic aromatic hydrocarbons (PAHs) and metals in Zagreb, Croatia. Daily concentrations of PM10, selected PAHs, metals and NO2 from four monitoring stations (2017–2020) were combined with local and ERA5 meteorology, highway traffic counts and gas consumption as emission proxies. Non-negative Matrix Factorization (NMF) was applied separately to PAHs and metals to identify dominant source-related patterns, while Random Forest regression and SHapley Additive Explanations (SHAP) were used to evaluate the influence of temporal, spatial, meteorological, traffic and heating predictors. NMF separated a heating-related PAH component dominated by Pyr and Flu from a traffic-related component characterised by BaA, Chry and BkF, and indicated enrichment of As and Pb at traffic- and industry-affected stations. Random Forest models showed higher predictive skill for PAHs (R2 ≈ 0.60–0.68) than for metals (R2 ≈ 0.24–0.42). Temperature and solar radiation were the main predictors for PAHs, whereas PM10, NO2 and station indicators dominated the prediction of metals. These results demonstrate that integrating proxy emission indicators with explainable machine learning provides an efficient framework for characterising sources and supports season- and location-specific air quality management in data-limited urban environments.
城市地区的空气污染来自多个相互作用的来源,并受到气象的强烈影响,但直接排放数据往往不完整。本研究量化了克罗地亚萨格勒布的气象条件、监测站位置以及交通和住宅供暖的代理指标对pm10结合的多环芳烃(PAHs)和金属的影响。将2017-2020年4个监测站PM10、选定多环芳烃、金属和NO2的日浓度与当地和ERA5气象、公路交通计数和汽油消耗作为排放指标相结合。采用非负矩阵分解法(NMF)分别对多环烃和金属进行分析,确定优势源相关模式;采用随机森林回归法和SHapley加性解释法(SHAP)评估时间、空间、气象、交通和供暖预测因子的影响。NMF从以BaA、Chry和BkF为特征的交通相关成分中分离出了以Pyr和Flu为主的与供暖相关的PAH成分,并表明在受交通和工业影响的站点中存在As和Pb富集。随机森林模型对多环芳烃的预测能力(R2≈0.60 ~ 0.68)高于对金属的预测能力(R2≈0.24 ~ 0.42)。温度和太阳辐射是多环芳烃的主要预测因子,PM10、NO2和气象站指标是多环芳烃的主要预测因子。这些结果表明,将代理排放指标与可解释的机器学习相结合,为表征排放源提供了一个有效的框架,并支持数据有限的城市环境中特定季节和地点的空气质量管理。
{"title":"Assessment of contributors to airborne PAHs and heavy metals in PM10 using temporal, spatial, traffic and heating data in explainable machine learning models","authors":"Nikolina Račić ,&nbsp;Stanko Ružičić ,&nbsp;Valentino Petrić ,&nbsp;Teo Terzić ,&nbsp;Mario Antunović ,&nbsp;Ivan Škaro ,&nbsp;Gordana Pehnec ,&nbsp;Ivan Bešlić ,&nbsp;Ivana Jakovljević ,&nbsp;Zdravka Sever Štrukil ,&nbsp;Jasmina Rinkovec ,&nbsp;Silva Žužul ,&nbsp;Mario Lovrić","doi":"10.1016/j.aeaoa.2026.100413","DOIUrl":"10.1016/j.aeaoa.2026.100413","url":null,"abstract":"<div><div>Air pollution in urban areas originates from multiple interacting sources and is strongly influenced by meteorology, yet direct emission data are often incomplete. This study quantifies how meteorological conditions, station location, and proxy indicators of traffic and residential heating affect PM<sub>10</sub>-bound polycyclic aromatic hydrocarbons (PAHs) and metals in Zagreb, Croatia. Daily concentrations of PM<sub>10</sub>, selected PAHs, metals and NO<sub>2</sub> from four monitoring stations (2017–2020) were combined with local and ERA5 meteorology, highway traffic counts and gas consumption as emission proxies. Non-negative Matrix Factorization (NMF) was applied separately to PAHs and metals to identify dominant source-related patterns, while Random Forest regression and SHapley Additive Explanations (SHAP) were used to evaluate the influence of temporal, spatial, meteorological, traffic and heating predictors. NMF separated a heating-related PAH component dominated by Pyr and Flu from a traffic-related component characterised by BaA, Chry and BkF, and indicated enrichment of As and Pb at traffic- and industry-affected stations. Random Forest models showed higher predictive skill for PAHs (R<sup>2</sup> ≈ 0.60–0.68) than for metals (R<sup>2</sup> ≈ 0.24–0.42). Temperature and solar radiation were the main predictors for PAHs, whereas PM<sub>10</sub>, NO<sub>2</sub> and station indicators dominated the prediction of metals. These results demonstrate that integrating proxy emission indicators with explainable machine learning provides an efficient framework for characterising sources and supports season- and location-specific air quality management in data-limited urban environments.</div></div>","PeriodicalId":37150,"journal":{"name":"Atmospheric Environment: X","volume":"29 ","pages":"Article 100413"},"PeriodicalIF":3.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of the area-based assimilative capacity for sustainability management of air toxic emission from petroleum and petrochemical industrial complex 发展以区域为基础的吸收能力,以可持续管理石油和石化工业综合体的空气有毒排放物
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2026-01-01 DOI: 10.1016/j.aeaoa.2025.100409
Peemapat Jookjantra , Sarawut Thepanondh , Kiyoung Lee , Jutarat Keawboonchu , Wissawa Malakan
This study explored benzene and 1,3-butadiene emissions from a petroleum and petrochemical industrial estate in Rayong, Thailand, using a comprehensive, multi-step approach. The research combined detailed emission inventories, air dispersion modeling with AERMOD which is appropriate for assessing primary, non-reactive pollutants at near-field distances from industrial sources, and evaluations of the area's capacity to absorb pollutants. The objective was to identify emission patterns, assess environmental impacts, and pinpoint the main sources influencing pollutant levels. Results showed that storage tanks were the primary driver of benzene emissions (54 %) and wastewater treatment systems were the main source of 1,3-butadiene emissions (63 %), with source analysis confirming that benzene levels were dominated by storage tanks while 1,3-butadiene concentrations were closely tied to wastewater treatment facilities. Although most predicted ground-level concentrations complied with national ambient air quality standards, elevated levels were detected near emission sources. The assimilative capacity assessment indicated that most monitoring sites could accommodate additional emissions without exceeding regulatory limits; however, one site located beside a busy road showed a negative capacity for both pollutants, highlighting the significant impact of vehicle emissions in areas with dense industrial and traffic activities. By integrating emission inventories, dispersion modeling, and environmental thresholds, this study offers valuable insights relevant locally and transferable to other industrial regions. It stresses the importance of emission control strategies targeting both industrial processes and traffic sources. The combined methodology provides practical guidance for environmental planners and policymakers seeking to implement effective, site-specific air quality management aligned with sustainable development goals.
本研究探讨了苯和1,3-丁二烯排放从石油和石化产业在泰国罗勇,使用一个全面的,多步骤的方法。该研究结合了详细的排放清单、空气分散模型和AERMOD,该模型适用于评估工业源近场距离的主要非反应性污染物,并评估该地区吸收污染物的能力。目标是查明排放模式,评估环境影响,并查明影响污染物水平的主要来源。结果表明,储罐是苯排放的主要来源(54%),废水处理系统是1,3-丁二烯排放的主要来源(63%),污染源分析证实,苯水平主要由储罐控制,而1,3-丁二烯浓度与废水处理设施密切相关。虽然大多数预测的地面浓度符合国家环境空气质量标准,但在排放源附近检测到浓度升高。同化能力评价表明,大多数监测点可以容纳额外的排放而不超过管制限制;然而,位于繁忙道路旁的一个场地显示出两种污染物的负容量,突出了汽车排放对工业和交通活动密集地区的重大影响。通过整合排放清单、分散模型和环境阈值,本研究提供了与当地相关并可转移到其他工业区域的宝贵见解。它强调了针对工业过程和交通源的排放控制战略的重要性。综合方法为环境规划者和决策者寻求实施有效的、符合可持续发展目标的特定地点空气质量管理提供了实用指导。
{"title":"Development of the area-based assimilative capacity for sustainability management of air toxic emission from petroleum and petrochemical industrial complex","authors":"Peemapat Jookjantra ,&nbsp;Sarawut Thepanondh ,&nbsp;Kiyoung Lee ,&nbsp;Jutarat Keawboonchu ,&nbsp;Wissawa Malakan","doi":"10.1016/j.aeaoa.2025.100409","DOIUrl":"10.1016/j.aeaoa.2025.100409","url":null,"abstract":"<div><div>This study explored benzene and 1,3-butadiene emissions from a petroleum and petrochemical industrial estate in Rayong, Thailand, using a comprehensive, multi-step approach. The research combined detailed emission inventories, air dispersion modeling with AERMOD which is appropriate for assessing primary, non-reactive pollutants at near-field distances from industrial sources, and evaluations of the area's capacity to absorb pollutants. The objective was to identify emission patterns, assess environmental impacts, and pinpoint the main sources influencing pollutant levels. Results showed that storage tanks were the primary driver of benzene emissions (54 %) and wastewater treatment systems were the main source of 1,3-butadiene emissions (63 %), with source analysis confirming that benzene levels were dominated by storage tanks while 1,3-butadiene concentrations were closely tied to wastewater treatment facilities. Although most predicted ground-level concentrations complied with national ambient air quality standards, elevated levels were detected near emission sources. The assimilative capacity assessment indicated that most monitoring sites could accommodate additional emissions without exceeding regulatory limits; however, one site located beside a busy road showed a negative capacity for both pollutants, highlighting the significant impact of vehicle emissions in areas with dense industrial and traffic activities. By integrating emission inventories, dispersion modeling, and environmental thresholds, this study offers valuable insights relevant locally and transferable to other industrial regions. It stresses the importance of emission control strategies targeting both industrial processes and traffic sources. The combined methodology provides practical guidance for environmental planners and policymakers seeking to implement effective, site-specific air quality management aligned with sustainable development goals.</div></div>","PeriodicalId":37150,"journal":{"name":"Atmospheric Environment: X","volume":"29 ","pages":"Article 100409"},"PeriodicalIF":3.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
OPNet: A deep-learning approach for estimating particulate matter’s oxidative potential from satellite imagery OPNet:一种从卫星图像中估计颗粒物氧化电位的深度学习方法
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2025-12-17 DOI: 10.1016/j.aeaoa.2025.100406
Alessia Carbone , Ian Hough , Gemine Vivone , Jocelyn Chanussot , Rocco Restaino , Harry Dupont , Jean-Luc Jaffrezo , Gaëlle Uzu
The oxidative potential (OP) of particulate matter (PM) reflects its ability to trigger oxidative stress in the respiratory system and is increasingly recognised as a key metric for assessing PM toxicity. Concurrently, PM has gained importance as a health indicator, leading to its inclusion in European regulations. As OP is not routinely monitored at many sites, understanding exposure and related risks remains challenging. While satellite imagery is commonly used to estimate PM mass concentration, its application to OP has not yet been explored. We present a novel deep-learning-based approach employing satellite-based surface features for OP estimation, using both OPAA and OPDTT assays on 24-hour PM10 samples collected over five years in Grenoble (France). We propose OPNet, which consists of two parts: a deep backbone that extracts surface features from one satellite image, and a predictor estimating OPAA and OPDTT using the extracted features combined with contextual variables. The architecture is trained in two stages: in the domain-adaptive task, both are jointly trained to predict daily PM10 concentration, with the backbone initialised from weights from a general classification problem. In the domain-specific task, they are jointly updated to predict either OPAA or OPDTT, with the backbone initialised from the best weights obtained in the first stage. This approach explains up to 75% of the variance in OPAA and 58% in OPDTT when using both satellite imagery and auxiliary data. It offers a cost-effective solution to improve the estimation of OP, with implications for large-scale air quality monitoring and health impact assessments.
颗粒物(PM)的氧化电位(OP)反映了其在呼吸系统中引发氧化应激的能力,并且越来越被认为是评估PM毒性的关键指标。同时,PM作为一项健康指标变得越来越重要,导致其被纳入欧洲法规。由于许多地点没有常规监测OP,因此了解暴露和相关风险仍然具有挑战性。虽然卫星图像通常用于估算PM质量浓度,但尚未探索其在OP中的应用。我们提出了一种新的基于深度学习的方法,采用基于卫星的表面特征进行OP估计,使用OPAA和OPDTT对法国格勒诺布尔五年来收集的24小时PM10样本进行分析。我们提出了OPNet,它由两部分组成:从卫星图像中提取表面特征的深层骨干,以及使用提取的特征结合上下文变量估计OPAA和OPDTT的预测器。该体系结构分为两个阶段进行训练:在领域自适应任务中,两者都被联合训练以预测每日PM10浓度,骨架从一般分类问题的权重初始化。在特定领域的任务中,它们被联合更新以预测OPAA或OPDTT,并根据第一阶段获得的最佳权重初始化骨干。当同时使用卫星图像和辅助数据时,这种方法可以解释高达75%的OPAA差异和58%的OPDTT差异。它提供了一种具有成本效益的解决办法,以改进对OP的估计,从而对大规模空气质量监测和健康影响评估产生影响。
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引用次数: 0
Methodological factors affecting ammonia emission measurement with flux chambers from field-applied biogas digestate slurry (Technical note) 影响现场应用沼气沼液通量室测量氨排放的方法学因素(技术说明)
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2025-12-16 DOI: 10.1016/j.aeaoa.2025.100408
Johanna Pedersen , Sasha D. Hafner , Andreas S. Pacholski
This study evaluated technical factors influencing relative ammonia emissions following field application of biogas digestate using different slurry spreading methods. Experiments assessed: (i) slurry distribution uniformity across a trailing hose boom, (ii) the influence of driving speed, (iii) effects of hose spacing, and (iv) the effect of relocating dynamic flux chambers during measurement. Across all tests realistic application rates and representative field conditions were ensured. Results demonstrate that careful equipment setup, particularly hose selection and consistent spacing, minimized variability in measured emissions and dynamic flux chamber relocation elevated measured emissions. These findings provide practical guidance for experimental design and emission mitigation under typical farming conditions.
本研究对沼气池采用不同撒浆方式进行现场应用后影响相对氨排放的技术因素进行了评价。实验评估了:(i)尾水管臂上泥浆分布均匀性,(ii)行驶速度的影响,(iii)软管间距的影响,以及(iv)在测量过程中重新定位动态通量室的影响。在所有测试中,确保了实际的应用率和具有代表性的现场条件。结果表明,仔细的设备设置,特别是软管的选择和一致的间距,最小化了测量排放的变化,动态通量室的重新安置提高了测量排放。这些发现为典型农业条件下的试验设计和减排提供了实用指导。
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引用次数: 0
Using low-cost sensors for source attribution and health assessment: An air quality study in Brownsville, Texas 使用低成本传感器进行来源归属和健康评估:德克萨斯州布朗斯维尔的一项空气质量研究
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2025-12-05 DOI: 10.1016/j.aeaoa.2025.100405
Sai Deepak Pinakana , Kabir Bahadur Shah , Daniel Jaffe , Juan L. Gonzalez , Owen Temby , Gabriel Ibarra-Mejia , Amit U. Raysoni
Air quality monitoring remains a challenge in areas lacking or having sparse federal monitoring infrastructure, posing significant barriers to public health research. This study demonstrates the usage of low-cost sensors in addressing gaps in air quality monitoring, source attribution, and health risk assessment in a Brownsville, TX neighborhood impacted by emissions from a barite and celestite mineral processing unit. PM2.5 concentrations were measured using PurpleAir sensors deployed across three residential locations, with the site nearest to the processing unit recording a 24-h averaged PM2.5 concentration of 25.12 μg/m3—approximately 2.79 times higher than the nearest Texas Commission of Environmental Quality (TCEQ) CAMS (Continuous Ambient Monitoring Station) site. Indoor air quality was also evaluated in two of the residential units to characterize the influence of outdoor pollution on indoor microenvironment. The local wind data was used to conduct source attribution, and the results suggested that the mineral processing entity located south of the neighborhood was the likely source of particulate pollution in this middle-income neighborhood. A health risk assessment for PM2.5 exposure was conducted, and the results indicate a hazard quotient level below unity, suggesting low-risk non-carcinogenic effects on the community. This study underscores the pivotal role of low-cost sensors in generating localized air quality data, and their potential to support ameliorative evidence-based interventions.
在缺乏或联邦监测基础设施很少的地区,空气质量监测仍然是一项挑战,对公共卫生研究构成重大障碍。该研究展示了低成本传感器在解决德克萨斯州布朗斯维尔附近受重晶石和天青石矿物加工装置排放影响的空气质量监测、来源归属和健康风险评估方面的差距。PM2.5浓度测量使用了部署在三个居民区的PurpleAir传感器,最靠近处理单元的站点记录的24小时平均PM2.5浓度为25.12 μg/m3,比最近的德克萨斯州环境质量委员会(TCEQ) CAMS(连续环境监测站)站点高约2.79倍。还对其中两个住宅单元的室内空气质量进行了评价,以表征室外污染对室内微环境的影响。利用当地的风力数据进行源归因,结果表明,位于社区南部的选矿实体可能是该中等收入社区颗粒物污染的来源。对PM2.5暴露进行了健康风险评估,结果显示危害商水平低于1,表明对社区的低风险非致癌性影响。这项研究强调了低成本传感器在产生局部空气质量数据方面的关键作用,以及它们支持改进的循证干预措施的潜力。
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引用次数: 0
Estimating air emissions from animal production in the United States using statistical models: Ammonia emissions from swine grow-finish barns 使用统计模型估算美国动物生产过程中的空气排放:猪生长肥育场的氨排放
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2025-12-05 DOI: 10.1016/j.aeaoa.2025.100404
Ian C. Rumsey , Maliha N. Nash , John T. Walker
Animal production has the potential to emit various atmospheric pollutants including ammonia (NH3), which can impact human health, atmospheric visibility and ecosystem health through gaseous NH3 and associated NH4+ particulate matter deposition. Emission estimating methodologies were developed using statistical models to estimate daily NH3 emissions from swine grow-finish barns based on National Air Emissions Monitoring Study (NAEMS) data. Models were developed with variables that represented production, manure management and environmental conditions. Model performance was evaluated for predicting NAEMS and non-NAEMS emissions, consistency of model coefficients and sensitivity to different model input values. Accounting for ease of variable measurement, the best performing models for predicting NAEMS emissions were models 1b and 16a, both of which accounted for the influence of temperature, swine inventory and weight, but used different predictor and response variables. In predicting NAEMS emissions, model 1b had mean error (ME) and mean bias (MB) values of 1.6 kg day−1 (normalized mean error (NME) = 25.9 %) and 0.1 kg day−1 (normalized mean bias (NMB) = 1.2 %), respectively, which were slightly lower than the corresponding values for model 16a (ME/NME = 1.8 kg day−1/25.9 % and MB/NMB = 0.4 kg day−1/5.8 %). Model 1b performed better in predicting non-NAEMS emissions, but model 16a had more reasonable sensitivity when barn live animal weight was >215,000 kg. Models using nitrogen feed intake as a predictor variable also performed well in predicting emissions and although these models have greater uncertainty due to limited NAEMS measurements, they could potentially account for changes in feed practices.
动物生产有可能排放包括氨(NH3)在内的各种大气污染物,这些污染物可以通过气态NH3和相关的NH4+颗粒物沉积影响人类健康、大气能见度和生态系统健康。基于国家空气排放监测研究(NAEMS)数据,采用统计模型估算生猪育肥场每日NH3排放量,开发了排放估算方法。模型采用代表生产、粪肥管理和环境条件的变量。评估了模型预测NAEMS和非NAEMS排放的性能、模型系数的一致性以及对不同模型输入值的敏感性。考虑到变量测量的容易性,预测NAEMS排放的最佳模型是1b和16a模型,这两个模型都考虑了温度、猪存栏和体重的影响,但使用了不同的预测变量和响应变量。在预测NAEMS排放时,模型1b的平均误差(ME)和平均偏差(MB)值分别为1.6 kg day - 1(归一化平均误差(NME) = 25.9%)和0.1 kg day - 1(归一化平均偏差(NMB) = 1.2%),略低于模型16a的相应值(ME/NME = 1.8 kg day - 1/ 25.9%和MB/NMB = 0.4 kg day - 1/ 5.8%)。模型1b对非naems排放的预测效果较好,而模型16a在畜舍活畜体重为21.5万kg时具有更合理的敏感性。使用氮采食量作为预测变量的模型在预测排放方面也表现良好,尽管由于有限的NAEMS测量,这些模型具有更大的不确定性,但它们可能解释饲料实践的变化。
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引用次数: 0
Spatial heterogeneity and sources of atmospheric carbonyls during ozone episodes in the Pearl River Delta 珠江三角洲臭氧事件期间大气羰基的空间异质性及来源
IF 3.4 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2025-12-01 DOI: 10.1016/j.aeaoa.2025.100400
Lei Wei , Daocheng Gong , Chengliang Zhang , Zhuo Yan , Yu Wang , Qinqin Li , Chunlin Zhang , Shuo Deng , Yunfeng Liu , Yiming Zhao , Guanghui Li , Xujun Mo , Ruili Yang , Hao Wang , Boguang Wang
Carbonyls play critical roles in tropospheric photochemistry, significantly influencing radical budgets and ozone (O3) formation. Despite frequent O3 pollution episodes in the Pearl River Delta (PRD), the spatial heterogeneity and sources of carbonyls, particularly long-chain aliphatic saturated aldehydes (≥C6), remain poorly characterized. This study conducted large-scale grid-based sampling analysis of 23 carbonyls across 35 sites in the PRD during spring and autumn O3 pollution episodes in 2021. Higher concentrations were observed in the eastern PRD and Pearl River Estuary compared to the western PRD, with formaldehyde, acetaldehyde, acetone, and 2-butanone dominating the carbonyl profile. Short-chain carbonyls (C1 ∼ C5) exhibited strong correlations with industrial density, confirming anthropogenic dominance. Long-chain aldehydes showed non-biogenic characteristics, with significant contributions from cooking, shipping, and industrial processes involving fatty acids. Ozone formation potential analysis revealed that formaldehyde and acetaldehyde remained the principal contributors to O3 formation. However, the contribution of long-chain aldehydes was substantial at specific local sites (notably some rural locations), in some cases exceeding that of short-chain aldehydes. Our findings underscore the need for targeted control strategies addressing both short-chain and long-chain carbonyls, particularly from industrial and cooking-related sources.
羰基在对流层光化学中起关键作用,显著影响自由基收支和臭氧(O3)的形成。尽管珠江三角洲臭氧污染事件频繁发生,但羰基,特别是长链脂肪饱和醛(≥C6)的空间异质性和来源特征仍然很差。本研究在2021年春季和秋季臭氧污染期间,对珠三角35个地点的23种羰基进行了大规模网格抽样分析。与珠三角西部相比,珠三角东部和珠江口的甲醛、乙醛、丙酮和2-丁酮的浓度较高。短链羰基(C1 ~ C5)与工业密度表现出很强的相关性,证实了人为的优势。长链醛表现出非生物源性特征,在烹饪、航运和涉及脂肪酸的工业过程中发挥了重要作用。臭氧形成潜力分析表明,甲醛和乙醛仍然是臭氧形成的主要贡献者。然而,长链醛在特定地点(特别是一些农村地点)的贡献是巨大的,在某些情况下超过了短链醛。我们的研究结果强调了针对短链和长链羰基的有针对性的控制策略的必要性,特别是来自工业和烹饪相关的来源。
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引用次数: 0
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Atmospheric Environment: X
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