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Harmonisation of methane isotope ratio measurements from different laboratories using atmospheric samples

Dasgupta, Bibhasvata; Menoud, Malika; Veen, Carina van der; Levin, Ingeborg; Veidt, Cordelia; Moossen, Heiko; Michel, Sylvia Englund; Sperlich, Peter; Morimoto, Shinji; Fujita, Ryo; Umezawa, Taku; Platt, Stephen Matthew; Zwaaftink, Christine Groot; Myhre, Cathrine Lund; Fisher, Rebecca; Lowry, David; Nisbet, Euan G.; France, James; Maisch, Ceres Woolley; Brailsford, Gordon; Moss, Rowena; Goto, Daisuke; Pandey, Sudhanshu; Houweling, Sander; Warwick, Nicola; Röckmann, Thomas

Abstract. Establishing interlaboratory compatibility among measurements of stable isotope ratios of atmospheric methane (δ13C-CH4 and δD-CH4) is challenging. Significant offsets are common because laboratories have different ties to the VPDB or SMOW-SLAP scales. Umezawa et al. (2018) surveyed numerous comparison efforts for CH4 isotope measurements conducted from 2003 to 2017 and found scale offsets of up to 0.5 ‰ for δ13C-CH4 and 13 ‰ for δD-CH4 between laboratories. This exceeds the World Meteorological Organisation Global Atmospheric Watch (WMO-GAW) network compatibility targets of 0.02 ‰ and 1 ‰ considerably. We employ a method to establish scale offsets between laboratories using their reported CH4 isotope measurements on atmospheric samples. Our study includes data from eight laboratories with experience in high-precision isotope ratio mass spectrometry (IRMS) measurements for atmospheric CH4. The analysis relies exclusively on routine atmospheric measurements conducted by these laboratories at high-latitude stations in the Northern and Southern Hemispheres, where we assume each measurement represents sufficiently well-mixed air at the latitude for direct comparison. We use two methodologies for interlaboratory comparisons: (I) assessing differences between time-adjacent observation data and (II) smoothing the observed data using polynomial and harmonic functions before comparison. The results of both methods are consistent, and with a few exceptions, the overall average offsets between laboratories align well with those reported by Umezawa et al. (2018). This indicates that interlaboratory offsets remain robust over multi-year periods. The evaluation of routine measurements allows us to calculate the interlaboratory offsets from hundreds, in some cases thousands of measurements. Therefore, the uncertainty in the mean interlaboratory offset is not limited by the analytical error of a single analysis but by real atmospheric variability between the sampling dates and stations. Using the same method, we assess this uncertainty by investigating measurements from four high-latitude sites analysed by the INSTAAR laboratory. After applying the derived interlaboratory offsets, we present a harmonised time series for δ13C-CH4 and δD-CH4 at high northern and southern latitudes, covering the period from 1988 to 2023.

2025

Kunnskapsgrunnlag for Mattilsynets arbeid med å beskytte drikkevann mot kjemisk og fysisk forurensning fra vindkraftverk på land

Alexander, Jan; Kvalem, Helen Engelstad; Mariussen, Espen; Ruus, Anders; Schlabach, Martin; Steffensen, Inger-Lise; Amlund, Heidi; Dahl, Lisbeth; Hannisdal, Rita; Olsen, Ann-Karin Hardie; Samdal, Ingunn Anita; Knutsen, Helle Katrine

Etablering av vindkraftverk på land kan medføre en risiko for drikkevann når installasjonene ligger i eller nær vanntilsigsområder til drikkevannskilder. Denne rapporten, utarbeidet av VKM på oppdrag fra Mattilsynet, gir Mattilsynet et kunnskapsbasert grunnlag for å stille krav til konsekvensutredninger og detaljplan for å beskytte drikkevannet.
Rapporten identifiserer potensielle farer for kjemisk og fysisk forurensning av drikkevann gjennom hele livsløpet til et vindkraftverk – fra planlegging og anleggsfase, til drift og avvikling. Den beskriver relevante lover og forskrifter, sentrale aktører og deres roller, og legger vekt på når og hvordan Mattilsynet kan involveres og komme med innspill i den kommunale planprosessen etter plan- og bygningsloven og i konsesjonsprosessen etter energiloven som forvaltes av NVE. Det er av stor betydning at Mattilsynet varsles og involveres tidlig i prosessen. Tiltakshaver må sørge for at risiko for forurensning av drikkevann og vanntilsigsområde utredes på en etterprøvbar måte, slik at Mattilsynet kan gi tydelige innspill til utredningen for å sikre at drikkevannshensyn er ivaretatt.

2025

Description and evaluation of airborne microplastics in the United Kingdom Earth System Model (UKESM1.1) using GLOMAP-mode

McErlich, Cameron; Goddard, Felix; Aves, Alex; Hardacre, Catherine; Evangeliou, Nikolaos; Hewitt, Alan J.; Revell, Laura E.

Abstract. Airborne microplastics are a recently identified atmospheric aerosol species with potential air quality and climate impacts, yet they are not currently represented in global climate models. Here, we describe the addition of microplastics to the aerosol scheme of the UK Earth System Model (UKESM1.1): the Global Model of Aerosol Processes (GLOMAP). Microplastics are included as both fragments and fibres across a range of aerosol size modes, enabling interaction with existing aerosol processes such as ageing and wet and dry deposition. Simulated microplastics have higher concentrations over land, but can be transported into remote regions including Antarctica despite no assumed emissions from these regions. Lifetimes range between ∼17 d to ∼1 h, with smaller, hydrophilic microplastics having longer lifetimes. Microplastics are present throughout the troposphere, and the smallest particles are simulated to reach the lower stratosphere in small numbers. Dry deposition is the dominant microplastic removal pathway, but greater wet deposition occurs for smaller hydrophilic microplastic, due to interactions with clouds. Although microplastics currently contribute a minor fraction of the total aerosol burden, their concentration is expected to increase in future if plastic production continues to increase, and as existing plastic waste in the environment degrades to form new microplastic. Incorporating microplastics into UKESM1.1 is a key step toward quantifying their current atmospheric impact and offers a framework for simulating future emission scenarios for an assessment of their long term impacts on air quality and climate.

2025

Airborne microplastics on the move: Urban Europe as a source to remote regions

Herzke, Dorte; Schmidt, Natascha; Lervik, Astrid Elise; Schulze, Dorothea; Celentano, Samuel; Eckhardt, Sabine; Arp, Hans Peter Heinrich; Evangeliou, Nikolaos

This study presents a comprehensive assessment of unique parallel measurements of surface airborne and deposited microplastics (AMPs) across urban and remote sites in Norway, employing pyrolysis-GC/MS for polymer-specific analysis. MPs were detected in nearly all samples, with significantly higher concentrations and fluxes observed in urban areas like Oslo, where tire wear particles (TWP) dominated (>90 % of AMP mass). Seasonal peaks in TWP coincided with the transition to winter tires, while remote sites showed consistent but lower AMP levels, indicating long-range transport (LRT) from European source regions. Parallel measurements of suspended and deposited AMPs revealed consistent polymer signatures, highlighting common sources and transport pathways. Although urban TWP contributions to PM2.5 were generally low, episodic events reached up to 30 %, raising concerns about human exposure. The dual dataset enabled a robust cross-validation of atmospheric loading estimates and facilitated integration into advanced transport models for remote sites. Our findings confirm AMPs as significant components of urban air pollution and subsequent carriers of chemical and biological contaminants to remote regions, emphasizing the need for targeted monitoring and mitigation strategies.

2025

Modulation of the Semi-Annual Oscillation by Stratospheric Sudden Warmings as Seen in the High-Altitude JAWARA Re-analyses

Zhang, Jiarong; Orsolini, Yvan; Sato, Kaoru

The semi-annual oscillation (SAO) dominates seasonal variability in the equatorial stratosphere and mesosphere. However, the seasonally dependent modulation of the SAO in the stratosphere (SSAO) and mesosphere (MSAO) by sudden stratospheric warmings (SSWs) in the Arctic has not been investigated in detail. In this study, we examine the seasonal evolution of the SAO during 16 major SSW events spanning 2004 to 2024 using the Japanese Atmospheric General Circulation Model for Upper Atmosphere Research Data Assimilation System Whole Neutral Atmosphere Re-analysis (JAWARA). Basic features of the SAO are well captured by JAWARA, as evidenced by the SSAO and MSAO appearing at around 50 km and 85 km, respectively. The different responses of the SAO to early and late winter SSWs are particularly strong during the Northern Hemisphere winter of 2023/24. Early winter SSWs tend to significantly intensify the westward SSAO, while late winter SSWs tend to weaken the eastward SSAO. Similarly, the eastward MSAO is amplified during early winter SSWs, whereas the westward MSAO is slightly weakened during late winter SSWs. The weak MSAO response is probably due to its smaller climatological magnitude. Modulation of the SAO by SSWs is related to meridional temperature changes during SSWs through the thermal wind balance. Our findings contribute to the understanding of coupling between the tropics and high latitudes, as well as interhemispheric coupling.

2025

State of the Climate in 2025: Global Climate

Dunn, R. J. H.; Blannin, J.; Willett, K. M.; Gobron, N.; Morris, G. A.; Ades, Melanie; Adler, Robert; Alexe, Mihai; Allan, Richard P.; Anderson, John; Anneville, Orlane; Aono, Yasuyuki; Arguez, Anthony; Armenteras-Pascual, Dolors; Arosio, Carlo; Asher, Elizabeth; Augustine, John A.; Azorin-Molina, Cesar; Baez-Villanueva, Oscar M.; Barichivich, Jonathan; Baron, Alexandre; Beck, Hylke E.; Bellouin, Nicolas; Benedetti, Angela; Blenkinsop, Stephen; Bock, Olivier; Bodin, Xavier; Bonte, Olivier; Bosilovich, Michael G.; Boucher, Olivier; Bowman, Kevin; Buehler, Sarah A.; Bunno, Ayaka; Byrne, Michael; Campos, Diego; Cappucci, Fabrizio; Carrea, Laura; Casado-Rodríguez, Jesús; Chang, Kai-Lan; Christiansen, Hanne H; Christy, John R.; Chung, Eui-Seok; Ciasto, Laura M.; Clingan, Scott; Coldewey-Egbers, Melanie; Cooley, Sarah; Cooper, Owen R.; Cornes, Richard C.; Covey, Curt; Crétaux, Jean-Francois; Crimmins, Theresa; Crotwell, Molly; Culpepper, Joshua; Cusicanqui, Diego; Davis, Sean M.; Jeu, Richard A. M. de; Laat, Jos de; Degenstein, Doug; Delaloye, Reynald; Tomaso, Enza Di; Dokulil, Martin T.; Donat, Markus G.; Dorigo, Wouter A.; Dugan, Hilary; Durre, Imke; Dutton, Geoff; Effertz, Peter; Enno, Sven-Erik; Estilow, Thomas W.; Estrella, Nicole; Fereday, David; Fioletov, Vitali E.; Flemming, Johannes; Formanek, Maud; Foster, Michael J.; Frederikse, Thomas; Frith, Stacey M.; Froidevaux, Lucien; Füllekrug, Martin; Gallemann, Thomas; Garforth, Judith; Garg, Jay; Ghent, Darren; Gollop, Amee; Good, Elizabeth; Goodman, Steven; Goto, Atsushi; Grimaldi, Stefania; Gruber, Alexander; Gu, Guojun; Guglielmin, Mauro; Haghdoost, Shekoofeh; Hahn, Sebastian; Haimberger, Leopold; Hall, Brad D.; Harlan, Merritt E.; Harris, Bethan L.; Harris, Ian; Hemming, Deborah L.; Ho, Shu-peng (Ben); Holliday, Rebecca; Holzworth, Robert; Horton, Radley M.; Hrbáček, Filip; Hu, Guojie; Inness, Antje; Isaksen, Ketil; John, Viju O.; Jones, Philip D.; Junod, Robert; Kääb, Andreas; Kaiser, Johannes; Kaufmann, Viktor; Kellerer-Pirklbauer, Andreas; Kent, Elizabeth C.; Khaykin, Sergey; Kidd, Richard; Kipling, Zak; Kirkpatrick, Sarah; Kondragunta, Shobha; Kovács, Dávid D.; Kraemer, Benjamin M.; Laas, Alo; Lan, Xin; Lantz, Kathleen O.; Lavers, David A.; Leibensperger, Eric; Lems, Johanna; Lennard, Chris; Levenson, Eric S.; Liley, Ben; Lo, Y. T. Eunice; Loeb, Norman G.; Loyola, Diego; Macara, Gregor; Magnin, Florence; Matsuzaki, Shin-Ichiro; Matthews, Tom; Mayer, Michael; McVicar, Tim R.; Mears, Carl A.; Menzel, Annette; Merchant, Christopher J.; Meyer, Michael F.; Miralles, Diego G.; Montzka, Stephan A.; Morice, Colin; Morino, Isamu; Mrekaj, Ivan; Mühle, Jens; Nance, D.; Nicolas, Julien P.; Noetzli, Jeannette; O’Keefe, John; Ollinik, Jessica Erin; Osborn, Timothy J.; Parrington, Mark; Pellet, Cécile; Pelto, Mauri; Pennington, Elyse; Petersen, Kyle; Phillips, Coda; Pierson, Don; Pinto, Izidine; Po-Chedley, Stephen; Pogliotti, Paolo; Polvani, Lorenzo; Preimesberger, Wolfgang; Price, Colin; Pulkkanen, Merja; Randel, William J.; Raymond, Colin; Remy, Samuel; Ricciardulli, Lucrezia; Richardson, Andrew D.; Robinson, David A.; Rodell, Matthew; Rodriguez-Fernandez, Nemesio; Rogers, Cassandra D.W.; Rohini, P.; Rosenlof, Karen H.; Rozanov, Alexei; Rozkošný, Jozef; Rusanovskaya, Olga O.; Rutishauser, This; Sabeerali, C. T.; Sakai, Tetsu; Salamon, Peter; Sánchez-Lugo, Ahira; Sawaengphokhai, Parnchai; Schenzinger, Verena; Schmid, Martin; Sezaki, Fumi; Shao, Xi; Sharma, Sapna; Shi, Lei; Shimaraeva, Svetlana V.; Shinohara, Ryuichiro; Silow, Eugene A.; Simmons, Adrian J.; Smith, Katie; Smith, Sharon L.; Soden, Brian J.; Sofieva, Viktoria; Soldo, Logan; Sreejith, O. P.; Stackhouse, Jr.; Stauffer, Ryan M.; Steinbrecht, Wolfgang; Steiner, Andrea K.; Stevens, Thea; Stoy, Paul C.; Streletskiy, Dmitry A.; Taha, Ghassan; Thackeray, Stephen J.; Thibert, Emmanuel; Timofeyev, Maxim A.; Tourpali, Kleareti; Tronquo, Emma; Tye, Mari R.; Urraca, Ruben; A, Ronald van der; Schrier, Gerard van der; VanScoy, Greta; Vliet, Arnold J. H. van; Veal, Karen; Verburg, Piet; Vernier, Jean-Paul; Vimont, Isaac J.; Viticchie, Bartolomeo; Vivero, Sebastián; Vömel, Holger; Vose, Russell S.; Wang, Donqian; Wang, Ray H. J.; Waring, Abigail Marie; Warnock, Taran; Weber, Mark; Wei, Zigang; Wiese, David N.; Wild, Jeannette D.; Williams, Earle; Wong, Takmeng; Wood, Tom; Woolway, Richard Iestyn; Worden, John; Yang, Kai; Yin, Xungang; Zeng, Zhenzhong; Zhao, Lin; Ziemke, Jerry R.; Ziese, Markus; Zotta, Ruxandra-Maria; Zou, Cheng-Zhi

2025

Industrial and public infrastructure as local sources of organic contaminants in the Arctic

Evenset, Anita; Wit, Cynthia de; C.G. Muir, Derek; Elena Barbaro, ; Hippel, Frank von; Gabrielsen, Geir W.; Breedveld, Gijs D.; M Kirkelund, Gunvor; Langberg, Håkon Austad; Lyche, Jan Ludvig; Katrin Vorkamp, ; Pedersen, Kristine B.; Reiersen, Lars Otto; J Gunnarsdottir, Maria; Nicoletta Ademollo, ; Erland Jensen, Pernille; Roland Kallenborn, ; Simonetta Corsolini, ; Nash, Susan Bengtson; Hartz, William Frederik; Yi-Fan Li, ; Zifeng Zhang,

Arctic pollution has been a focal point in environmental research over the past five decades. Recently, the number of pollutants identified as relevant to the Arctic has significantly increased. Consequently, the expert group on Persistent Organic Pollutants (POPs) and Chemicals of Emerging Arctic Concern (CEACs) of the Arctic Monitoring and Assessment Programme (AMAP) has prepared a series of assessments of contaminants in the Arctic, including influences of climate change. This review addresses local sources of Arctic organic pollutants associated with infrastructure in the Arctic. Industrial, military, and public infrastructures, including domestic installations, sewage treatment, solid waste management, and airports, were identified as significant local pollution sources. Additionally, operational emissions (e.g., from shipping, transportation, heating, and power production) contribute to the overall local pollution profile. Based on currently available scientific information, elevated POP and CEAC levels are mostly found in close proximity to identified local pollution sources. To date, hazardous effects have only been confirmed for a few selected chemicals, such as polycyclic aromatic compounds (PAC) and certain pharmaceutical residues. However, studies are biased in the sense that they often focus on well-known contaminants, at a risk of overlooking CEAC and their effects. The review identifies several measures to reduce human impacts on local Arctic environments, including (i) using local indicator pollutants in ongoing national monitoring schemes, (ii) harmonizing emission reduction policies and licensing of industrial activities in the region to minimize exposure risks and environmental pollution, (iii) encouraging local municipalities, industries, and related stakeholders to coordinate their activities to minimize pollutant emissions.

2025

Quantifying European SF6 emissions from 2005 to 2021 using a large inversion ensemble

Vojta, Martin; Plach, Andreas; Thompson, Rona Louise; Purohit, Pallav; Stanley, Kieran; O'Doherty, Simon; Young, Dickon; Pitt, Joe; Arduini, Jgor; Lan, Xin; Stohl, Andreas

Abstract. Sulfur hexafluoride (SF6) is a highly potent and long-lived greenhouse gas whose atmospheric concentrations are increasing due to human emissions. In this study, we determine European SF6 emissions from 2005 to 2021 using a large ensemble of atmospheric inversions. To assess uncertainty, we systematically vary key inversion parameters across 986 sensitivity tests and apply a Monte Carlo approach to randomly combine these parameters in 1003 additional inversions. Our analysis focuses on high-emitting countries with robust observational coverage – UK, Germany, France, and Italy – while also examining aggregated EU-27 emissions. SF6 emissions declined across all studied regions except Italy, largely attributed to EU F-gas regulations (2006, 2014), however, national reports underestimated emissions: (i) UK emissions dropped from 68 (47–77) t yr−1 in 2008 to 19 (15–26) t yr−1 in 2018, aligning with the reports from 2018 onward; (ii) French emissions fell from 78 (51–117) t yr−1 (2005) to 35 (19–54) t yr−1 (2021), exceeding reports by 88 %; (iii) Italian emissions fluctuated (25–48 t yr−1), surpassing reports by 107 %; (iv) German emissions declined from 182 (155–251) t yr−1 (2005) to 97 (88–104) t yr−1 (2021), aligning reasonably well with reports; (v) EU-27 emissions decreased from 403 (335–501) t yr−1 (2005) to 225 (191–260) t yr−1 (2021), exceeding reports by 20 %. A substantial drop from 2017 to 2018 mirrored the trend in southern Germany, suggesting regional actions were taken as the 2014 EU regulation took effect. Our sensitivity tests highlight the crucial role of dense monitoring networks in improving inversion reliability. The UK system expansions (2012, 2014) significantly enhanced result robustness, demonstrating the importance of comprehensive observational networks in refining emission estimates.

2025

Biomethanol as a Marine Fuel Within Land Use Sustainability Boundaries

Esfandiari, Homa; Muri, Helene; Kramel, Diogo

Global shipping is an essential, energy-efficient enabler of trade, yet it remains a hard-to-abate sector. With shipping demand projected to continue to rise in the coming decades, identifying scalable and sustainable fuel alternatives is critical. Biofuels, and particularly biomethanol, offer a promising option due to their compatibility with existing infrastructure. However, their sustainability critically hinges on land use impacts. From this Perspective, we argue that biomethanol derived from a dedicated crop could contribute to maritime decarbonisation, with ~71–77% well-to-wake greenhouse gases (GHG) reductions under cropland-only constraints. We further point to the fact that a wider adoption faces challenges such as higher costs, limited availability, and lower energy density relative to fossil fuels. Continued research and monitoring are essential to ensure that biofuel production does not inadvertently contribute to deforestation or biodiversity loss. We underscore the need for spatially sensitive biofuel deployment strategies that align maritime decarbonisation with land-system sustainability and climate objectives.

2025

Machine-Learning-Driven Reconstruction of Organic Aerosol Sources across Dense Monitoring Networks in Europe

Jouanny, Adrien; Upadhyay, Abhishek; Jiang, Jianhui; Vasilakos, Petros; Via, Marta; Cheng, Yun; Flueckiger, Benjamin; Uzu, Gaëlle; Jaffrezo, Jean-Luc; Voiron, Céline; Favez, Olivier; Chebaicheb, Hasna; Bourin, Aude; Font, Anna; Riffault, Véronique; Freney, Evelyn; Marchand, Nicolas; Chazeau, Benjamin; Conil, Sébastien; Petit, Jean-Eudes; Rosa, Jesús D. de la; Campa, Ana Sanchez de la; Navarro, Daniel Sanchez-Rodas; Castillo, Sonia; Alastuey, Andrés; Querol, Xavier; Reche, Cristina; Minguillón, María Cruz; Maasikmets, Marek; Keernik, Hannes; Giardi, Fabio; Colombi, Cristina; Cuccia, Eleonora; Gilardoni, Stefania; Rinaldi, Matteo; Paglione, Marco; Poluzzi, Vanes; Massabò, Dario; Belis, Claudio; Grange, Stuart; Hueglin, Christoph; Canonaco, Francesco; Tobler, Anna; Timonen, Hilkka J.; Aurela, Minna; Ehn, Mikael; Stavroulas, Iasonas; Bougiatioti, Aikaterini; Eleftheriadis, Konstantinos; Gini, Maria I.; Zografou, Olga; Manousakas, Manousos-Ioannis; Chen, Gang Ian; Green, David Christopher; Pokorná, Petra; Vodička, Petr; Lhotka, Radek; Schwarz, Jaroslav; Schemmel, Andrea; Atabakhsh, Samira; Herrmann, Hartmut; Poulain, Laurent; Flentje, Harald; Heikkinen, Liine; Kumar, Varun; Gon, Hugo Anne Denier van der; Aas, Wenche; Platt, Stephen Matthew; Yttri, Karl Espen; Salma, Imre; Vasanits, Anikó; Bergmans, Benjamin; Sosedova, Yulia; Necki, Jaroslaw; Ovadnevaite, Jurgita; Lin, Chunshui; Pauraite, Julija; Pikridas, Michael; Sciare, Jean; Vasilescu, Jeni; Belegante, Livio; Alves, Célia; Slowik, Jay G.; Probst-Hensch, Nicole; Vienneau, Danielle; Prévôt, André S. H.; Medbouhi, Aniss Aiman; Banos, Daniel Trejo; Hoogh, Kees de; Daellenbach, Kaspar R.; Krymova, Ekaterina; Haddad, Imad El

Fine particulate matter (PM) poses a major threat to public health, with organic aerosol (OA) being a key component. Major OA sources, hydrocarbon-like OA (HOA), biomass burning OA (BBOA), and oxygenated OA (OOA), have distinct health and environmental impacts. However, OA source apportionment via positive matrix factorization (PMF) applied to aerosol mass spectrometry (AMS) or aerosol chemical speciation monitoring (ACSM) data is costly and limited to a few supersites, leaving over 80% of OA data uncategorized in global monitoring networks. To address this gap, we trained machine learning models to predict HOA, BBOA, and OOA using limited OA source apportionment data and widely available organic carbon (OC) measurements across Europe (2010–2019). Our best performing model expanded the OA source data set 4-fold, yielding 85 000 daily apportionment values across 180 sites. Results show that HOA and BBOA peak in winter, particularly in urban areas, while OOA, consistently the dominant fraction, is more regionally distributed with less seasonal variability. This study provides a significantly expanded OA source data set, enabling better identification of pollution hotspots and supporting high-resolution exposure assessments.

2025

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