Christine A. Harper, , , Linda Arterburn, , , Katherine Paredero, , , Rime El Asmar, , , Mariama L. Stewart, , , David J. Tanner, , , James M. Roberts, , , John J. Orlando, , , Joseph Sadighi, , , Rodney J. Weber, , and , L. Gregory Huey*,
{"title":"Observations of the Gas Phase Composition of the 2024 BioLab Industrial Plume in the Atlanta Metropolitan Area","authors":"Christine A. Harper, , , Linda Arterburn, , , Katherine Paredero, , , Rime El Asmar, , , Mariama L. Stewart, , , David J. Tanner, , , James M. Roberts, , , John J. Orlando, , , Joseph Sadighi, , , Rodney J. Weber, , and , L. Gregory Huey*, ","doi":"10.1021/acs.estlett.6c00160","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00160","url":null,"abstract":"<p >A fire at a pool chemical manufacturing facility in Conyers, Georgia, on September 29, 2024, released a persistent chemical plume that impacted the Atlanta metropolitan area, causing evacuation of more than 17,000 people. We used chemical ionization mass spectrometry (HR-TOF-CIMS) in Midtown Atlanta (21 miles from the facility), and in Conyers (quadrupole CIMS) to characterize plume composition. We observed unexpectedly high concentrations of Br<sub>2</sub> (up to 1.4 × 10<sup>2</sup> ppbv) dominating early plumes, along with elevated levels of HNCO (31 ppbv) and numerous other compounds. Twenty-six species were identified, including reactive nitrogen-containing compounds (e.g., HNCO, cyanoacetic acid, and cyanamide) and oxygenated volatile organic compounds (e.g., acetaldehyde). Br<sub>2</sub> concentrations in Midtown exceeded United States Environmental Protection Agency (EPA) 1 h Acute Exposure Guideline Levels (AEGL-1) thresholds by a factor of 4. Later measurements in Conyers showed Cl<sub>2</sub> reaching 3.7 × 10<sup>2</sup> ppbv during the second week. Given that Midtown observations were 21 miles downwind, concentrations near the source in Conyers were likely 2 orders of magnitude higher. This is the first comprehensive chemical characterization of a pool chemical decomposition plume revealing complexity beyond simple halogen release and highlighting health risks from simultaneous exposure to multiple respiratory irritants.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"664–669"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.estlett.6c00160","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Steffi Joseph Perumpully, , , Shikha Garg, , and , T. David Waite*,
{"title":"Is Thermal Activation of Peroxymonocarbonate (HCO4–) Important?","authors":"Steffi Joseph Perumpully, , , Shikha Garg, , and , T. David Waite*, ","doi":"10.1021/acs.estlett.6c00289","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00289","url":null,"abstract":"<p >Recently, activation of peroxymonocarbonate (HCO<sub>4</sub><sup>–</sup>), formed upon H<sub>2</sub>O<sub>2</sub>–HCO<sub>3</sub><sup>–</sup> interaction, by heat and/or catalyst has been reported to generate a suite of reactive species such as HO<sup>•</sup>, CO<sub>3</sub><sup>•–</sup>, and <sup>1</sup>O<sub>2</sub>. Here, we systematically examine the uncatalyzed thermal activation of HCO<sub>4</sub><sup>–</sup> across environmentally relevant pHs (8.3–10.3) and carbonate concentrations (0–10 mM) by measuring the degradation of a range of organic contaminants with differing reactivity toward HCO<sub>4</sub><sup>–</sup>, HO<sup>•</sup>, CO<sub>3</sub><sup>•–</sup>, and <sup>1</sup>O<sub>2</sub>. Our results show that, in the temperature range 20–60 °C, thermal activation of HCO<sub>4</sub><sup>–</sup> is negligible, with contaminant removal instead driven by trace Cu impurities that catalyze H<sub>2</sub>O<sub>2</sub> decomposition. Furthermore, Cu-mediated activation of HCO<sub>4</sub><sup>–</sup> is insignificant, indicating that the previously reported “HCO<sub>4</sub><sup>–</sup> activation” likely reflects secondary H<sub>2</sub>O<sub>2</sub> activation. Overall, these findings highlight the need for rigorous control of trace-metal impurities upon evaluation of uncatalyzed thermal activation of various oxidants/reductants. Furthermore, future studies on the catalytic activation of HCO<sub>4</sub><sup>–</sup> must provide direct, unambiguous evidence of the role of HCO<sub>4</sub><sup>–</sup> because carbonate-dependent effects on the oxidative performance do not necessarily indicate that HCO<sub>4</sub><sup>–</sup> is involved.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"773–779"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147864981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Model for Dry Deposition of Atmospheric Micro- and Nanoplastic Fibers","authors":"Hosein Foroutan*, ","doi":"10.1021/acs.estlett.6c00165","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00165","url":null,"abstract":"<p >Atmospheric microplastics and nanoplastics (MNPs), particularly fibers, are emerging contaminants with complex deposition dynamics that remain poorly understood. Here, a mechanistic dry deposition model is developed for MNP fibers, integrating gravitational settling, Brownian diffusion, impaction, and interception. The model incorporates fiber-specific drag corrections and shape-dependent diffusivity to estimate total deposition velocity across a range of particle lengths and aspect ratios. Results show that total deposition velocity deviates significantly from gravitational settling alone, especially for submicron fibers. Global simulations reveal strong spatial and seasonal variability driven by land cover and turbulence. Atmospheric lifetime estimates based on dry deposition indicate that micro – nano transition fibers (∼ 1 μm) persist longest in the boundary layer, with dry-deposition lifetimes exceeding four months (∼ 2,900 h). This framework supports the integration of MNP fibers into existing aerosol dry-deposition schemes in regional and global atmospheric models and improves predictions of their environmental fate.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"737–743"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.estlett.6c00165","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865070","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Circadian Receptor-Guided Screening for Environmental Circadian Disruptor Discovery","authors":"Keda Jing, , , Ruohan Wang, , , Siyu Chen, , , Shaoqi Zuo, , , Kun Zhang, , , Jiayin Dai, , , Ximing Qin*, , and , Yanbin Zhao*, ","doi":"10.1021/acs.estlett.6c00221","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00221","url":null,"abstract":"<p >Circadian rhythm disruption has emerged as a potential environmental health concern, yet systematic strategies for identifying chemical perturbators of molecular clocks remain limited. In the present study, we developed a receptor-guided screening framework targeting two core circadian nuclear receptors, REV-ERBα and RORα, to prioritize environmental circadian disrupting chemicals. High-throughput virtual screening of ∼12,000 compounds from Tox21 and the Endocrine Disruptor Screening Program database revealed distinct chemical-receptor interaction patterns, with pharmaceuticals emerging as the most prominent category. Dual-luciferase assays then identified nine REV-ERBα-active compounds and nine RORα-active compounds that significantly modulated receptor-mediated transcriptional activity, including industrial plasticizer pentaerythritol tetrabenzoate (PTB) and SSRI antidepressant paroxetine. Notably, several compounds exhibited activity at low-micromolar concentrations and are frequently detected in water systems, suggesting potential ecological relevance. Functional validation using real-time bioluminescence monitoring further confirmed that representative hits, including PTB, induced robust and statistically significant alterations in circadian period in human U2OS cells. This study establishes a receptor-guided screening framework linking molecular interactions to cellular rhythmic outcomes and highlights circadian disruption as an emerging mechanistic end point for environmental chemical risk assessment.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"677–683"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nathaniel L. Scholz, , , Jay W. Davis, , , Julann A. Spromberg*, , , Blake E. Feist, , , Tiffany L. Linbo, , , Jana S. Labenia, , , James R. Cameron, , , Barbara L. French, , , David H. Baldwin, , , John P. Incardona, , and , Tracy K. Collier,
{"title":"The Origin Story for 6PPD-quinone in Ecotoxicology","authors":"Nathaniel L. Scholz, , , Jay W. Davis, , , Julann A. Spromberg*, , , Blake E. Feist, , , Tiffany L. Linbo, , , Jana S. Labenia, , , James R. Cameron, , , Barbara L. French, , , David H. Baldwin, , , John P. Incardona, , and , Tracy K. Collier, ","doi":"10.1021/acs.estlett.6c00205","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00205","url":null,"abstract":"<p >In 2020, an environmental transformation product of the synthetic tire additive N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD), or 6PPD-quinone, was identified as the causative chemical agent for a mysterious and recurring mass mortality syndrome affecting adult coho salmon (<i>Oncorhynchus kisutch</i>) as they returned from the ocean to spawn in restored urban streams. A few years hence, 6PPD-q and related tire chemicals have become a global research focus in aquatic ecotoxicology, environmental engineering, and public health. Here we review the two-decade forensic investigation that led to the discovery of 6PPD-q, including converging lines of evidence from field surveys, landscape modeling, stormwater bioassays, and green infrastructure effectiveness studies. As the body of knowledge around 6PPD-q rapidly grows, we consider implications for Pacific salmon conservation, stormwater management, river restoration, and urban ecology. Finally, we highlight research priorities identified by the authors to inform salmon recovery efforts in urbanizing watersheds that are increasingly impacted by polluted nonpoint source runoff.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"644–655"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.estlett.6c00205","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147864950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Cutting-Edge Environmental Genome Monitoring Shaping a New Era of Genome-Based Safety Research for One Health and Evolution","authors":"Hiroshi Honda*, , , Takayoshi Suzuki, , , Natsuko Ito Kondo, , , Kaede Miyata, , , Shunsuke Utsumi, , , Masami Yamada, , and , Masaaki Kitajima, ","doi":"10.1021/acs.estlett.5c00804","DOIUrl":"https://doi.org/10.1021/acs.estlett.5c00804","url":null,"abstract":"<p >Mutagenicity and genotoxicity research has traditionally focused on evaluating how chemicals affect genomes, particularly in relation to mutation-driven carcinogenesis. Advances in next-generation sequencing have broadened environmental applications, enabling eDNA/eRNA analysis, metagenomics, and wastewater-based surveillance for ecosystems and public health monitoring. Framed within a One Health perspective that links human, animal, and environmental health, this Global Perspective examines synergies between mutagenomics and environmental genomics aimed at maintaining organismal and ecosystem health. We review emerging trends across five domains including antimicrobial resistance genes, pathogen dynamics, biodiversity, environmental stress responses, and biological evolution and discuss how integrating mutation genomics and molecular toxicology techniques into environmental monitoring can address current gaps. Common challenges include sensitive detection of low-frequency variants in mixed environmental samples, functional interpretation and causal attribution of variants and expression changes, and the lack of cross-taxonomic reference resources. Overcoming these challenges with mutation-genomics-derived approaches could enable improved source attribution, earlier detection of emerging threats, and outcome-oriented risk assessment. Now is the time to strengthen interdisciplinary collaboration, standardize methods, and establish cross-taxonomic reference and analytical infrastructures.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"618–626"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147871412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Decadal Shift in the Secondary Organic Aerosol Response to Winter Haze Mitigation in Eastern China: Insights from Aerosol Mass Spectrometry Measurements and Machine Learning","authors":"Yunjiang Zhang*, , , Zeye Liang, , , Jie Fang, , , Jingyi Li, , , Ming Wang, , , Bo Zheng, , , Songshan Du, , , Cheng Chen, , , Didier Hauglustaine, , , Jean-Eudes Petit, , , Olivier Favez, , , Hongli Wang, , , Mindong Chen, , and , Xinlei Ge*, ","doi":"10.1021/acs.estlett.5c01047","DOIUrl":"https://doi.org/10.1021/acs.estlett.5c01047","url":null,"abstract":"<p >Organic aerosols are an important and highly dynamic component of fine particulate matter, yet their long-term response to emission controls is poorly constrained. We analyze a decade (2013–2023) of wintertime aerosol mass spectrometry data from urban Nanjing, eastern China, using a developed machine learning framework that disentangles anthropogenic emission-driven changes from meteorology-driven changes. The mean organic aerosol concentrations decreased from 24.6 to 16.5 μg m<sup>–3</sup> during the period of 2013–2017. After accounting for meteorological influences, emission controls account for ∼94% of the observed decrease. However, the effectiveness of anthropogenic emission controls on the total organic aerosol was weakened by a factor of approximately 2–8 times in the subsequent emission control phases, particularly with more oxidized secondary organic aerosol showing a minimal further decrease. Machine learning-based attribution analysis reveals that reductions in fossil fuel combustion and traffic-related aromatic precursors explain, on average, ∼50–60% of the long-term variability in secondary organic aerosol, while the meteorological influence plays a minor role. These results provide observationally source-resolved evidence that current measures are reaching diminishing returns and that effective future controls must target overlooked precursors and secondary formation pathways.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"698–705"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anna Jonsson Sundberg*, , , Daniel Cerveny, , , Federico Costa, , , Mike Begon, , , Fabio Neves Souza, , , Jaqueline S. Cruz, , , Caio Graco Zeppelini, , , Hernan D. Argibay, , , Ianei de Oliveira Carneiro, , , Albert I. Ko, , , Mitermayer G. Reis, , , Erin S. McCallum, , and , Hussein Khalil*,
{"title":"Pharmaceutical Pollutants in Urban Rats Are Linked to Zoonotic Infection Risk","authors":"Anna Jonsson Sundberg*, , , Daniel Cerveny, , , Federico Costa, , , Mike Begon, , , Fabio Neves Souza, , , Jaqueline S. Cruz, , , Caio Graco Zeppelini, , , Hernan D. Argibay, , , Ianei de Oliveira Carneiro, , , Albert I. Ko, , , Mitermayer G. Reis, , , Erin S. McCallum, , and , Hussein Khalil*, ","doi":"10.1021/acs.estlett.5c00867","DOIUrl":"https://doi.org/10.1021/acs.estlett.5c00867","url":null,"abstract":"<p >Pharmaceutical pollution is globally widespread and known to affect the biology and ecology of exposed wildlife. However, its effects on wildlife disease, including zoonotic (animal-to-human transmitted) infections, remains unclear. We examined the presence of 97 Active Pharmaceutical Ingredients (APIs) and their associations with zoonotic infections (<i>Leptospira</i> spp., Seoul orthohantavirus, <i>Toxoplasma gondii</i>, <i>Capillaria</i> spp., and <i>Angiostrongylus</i> spp.) in <i>Rattus norvegicus</i> and <i>R. rattus</i> rats, two globally distributed zoonotic reservoirs. We collected 152 rats from low-income urban communities in Salvador, Brazil, and detected APIs in 55.3% of the rats’ brain tissues, providing novel evidence of pharmaceutical uptake in a wild, terrestrial mammal. Notably, <i>Leptospira</i> infection was 91% lower in rats containing the antibiotic azithromycin, while detection of antidepressant citalopram corresponded to a 3-fold increase in <i>Capillaria</i> infection risk. Our findings show that environmental APIs absorbed by rats are associated with variation in zoonotic infection risk, representing a previously unrecognized pathway through which pharmaceutical pollution may influence disease dynamics in cities worldwide.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"656–663"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.estlett.5c00867","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865045","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ella Milliken*, , , Alex Woodley, , and , Noah Planavsky,
{"title":"Soil Carbon Dioxide Removal Estimates from Enhanced Weathering Deployments in the Southeastern United States Are Likely Tied to Cation Mobility","authors":"Ella Milliken*, , , Alex Woodley, , and , Noah Planavsky, ","doi":"10.1021/acs.estlett.5c01172","DOIUrl":"https://doi.org/10.1021/acs.estlett.5c01172","url":null,"abstract":"","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"782–785"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.estlett.5c01172","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Domestic Liquefied Petroleum Gas and Natural Gas Stoves as an Important Source of Indoor and Outdoor HONO and NOx","authors":"Wenting Yuan, , , Chao Pan, , , Weilin Huang, , , Ketan Xie, , , Lifang Zhang, , , Wangchao Zhao, , , Xiaoqiao Jiao, , , Bo Yang, , , Huizhong Shen, , , Bin Ye, , and , Chen Wang*, ","doi":"10.1021/acs.estlett.6c00059","DOIUrl":"https://doi.org/10.1021/acs.estlett.6c00059","url":null,"abstract":"<p >Liquefied petroleum gas (LPG) and natural gas (NG) stoves emit nitrous acid (HONO) and nitrogen oxides (NO<sub><i>x</i></sub>), two critical atmospheric pollutants, yet their emission characteristics and impacts are not fully understood. This study characterized HONO and NO<sub><i>x</i></sub> emissions and evaluated the influencing factors for both stove types. LPG combustion consistently demonstrated higher emission factors (EFs) than NG. At a high power, HONO and NO<sub><i>x</i></sub> EFs from LPG reached 110 ± 7 and 1476 ± 39 mg kg<sup>–1</sup> of fuel, respectively, compared to 56.0 ± 1.4 and 1032 ± 34 mg kg<sup>–1</sup> of fuel for NG. The emissions increased with the power level and duration but decreased in the presence of cookware, indicating previous simulations without cookware likely overestimated EFs. Moreover, NG combustion exhibited higher NO<sub>2</sub>/NO emission ratios (∼3.3) than LPG (∼0.7) across all power settings, attributable to the lower flame temperature of NG. The environmental impact of residential stoves extends beyond indoor air, contributing significantly to outdoors. For instance, HONO emissions from residential stoves (3.1 ± 0.1 kt year<sup>–1</sup>) exceed those from gasoline vehicles (0.6 ± 0.2 kt year<sup>–1</sup>) in China. These findings highlight the significance of domestic gas stoves in atmospheric chemistry and provide key data for refining the HONO emission inventories.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":"13 5","pages":"720–727"},"PeriodicalIF":8.8,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147865191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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