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Aging of Tire Particles in Deep-Sea Conditions: Interactions between Hydrostatic Pressure, Prokaryotic Growth and Chemical Leaching

Schmidt, Natascha; Foscari, Aurelio; Herzke, Dorte; Garel, Marc; Tamburini, Christian; Seiwert, Bettina; Reemtsma, Thorsten; Sempéré, Richard

Tire particles can enter the marine environment e.g. through direct discharge of road runoff, sewage systems or riverine inputs. Their fate in marine waters remains largely unknown, though the deep sea could be a final sink as for other marine litter. To simulate these conditions, we investigated in laboratory-controlled conditions the effects of high-hydrostatic pressure [20 MPa] vs atmospheric pressure [0.1 MPa] on the leaching of 17 organic compounds from cryo-milled tire tread particles (μm sized) and crumb rubber particles (mm sized) into natural seawater. We monitored the abundance of heterotrophic prokaryotes in the leachates over the 14 day exposure period under biotic conditions. Abiotic controls were employed to delineate the influence of prokaryotes on the fate of leached chemicals. Our results showed leaching of dissolved organic carbon and target chemicals under all experimental conditions, with higher concentrations of certain target chemicals under high-hydrostatic pressure conditions (e.g., 1,3-diphenylguanidine [DPG]: max. 703 (20 MPa) vs 119 μg/L (0.1 MPa) from cryo-milled tire tread particles under biotic conditions). Under abiotic conditions leaching was weaker for DPG and other chemicals, with contrasting trends for chemicals prone to biotransformation. In crumb rubber leachates chemical concentrations increased with time, but showed no significant differences between biotic/abiotic or high-hydrostatic/atmospheric pressure conditions. Prokaryotic abundance increased in all samples containing tire particles compared to seawater controls, indicating the use of the rubber and/or leached chemicals as an energy source.

2025

Divergent impacts of climate interventions on China’s north-south water divide

Zhang, Xiao; Fan, Yuanchao; Tjiputra, Jerry; Muri, Helene; Chen, Qiao

Abstract Solar radiation modification-based climate interventions may cause uneven regional hydrological changes while mitigating warming. Here, we investigate the effects of climate interventions on China’s North Drought-South Flood pattern using the Norwegian Earth System Model supplemented by volcanic data. Our results indicate that equatorial stratospheric aerosol injection could mitigate the north-south water divide by reducing inter-hemispheric and equator-to-North-pole temperature gradients, thereby modifying atmospheric circulation and the East Asian monsoon to increase precipitation and surface runoff in northern China while reducing them in the south, compared to the high emissions scenario. This mechanism is supported by observed precipitation changes following the Mount Pinatubo volcanic eruption. In contrast, marine cloud brightening may intensify southern flood risks, while cirrus cloud thinning and moderate emissions reduction might exacerbate northern droughts. Our findings reveal distinct regional hydroclimatic impacts of different climate interventions, highlighting potential synergies and trade-offs between their global intervention efficacy and regional water security.

2025

Analysis of source regions and transport pathways of sub-micron aerosol components in Europe

Schneider, Michelle Y.; Jiang, Jianhui; Chen, Ying; Aas, Wenche; Atabakhsh, Samira; Aurela, Minna; Belis, Claudio; Bougiatioti, Aikaterini; Bressi, Michael; Canonaco, Francesco; Chazeau, Benjamin; Chebaicheb, Hasna; Ehn, Mikael; Eleftheriadis, Konstantinos; Favez, Olivier; Flentje, Harald; Font, Anna; Freney, Evelyn; Gilardoni, Stefania; Gini, Maria I.; Green, David C.; Heikkinen, Liine; Keernik, Hannes; Lhotka, Radek; Lin, Chunshui; Maasikmets, Marek; Marchand, Nicolas; Minguillón, María Cruz; Necki, Jaroslaw; Ovadnevaite, Jurgita; Paglione, Marco; Pauraite, Julija; Petit, Jean-Eudes; Pikridas, Michael; Platt, Stephen Matthew; Pokorná, Petra; Poluzzi, Vanes; Poulain, Laurent; Riffault, Véronique; Rinaldi, Matteo; Sciare, Jean; Sosedova, Yulia; Stavroulas, Iasonas; Timonen, Hilkka; Tobler, Anna; Vasilescu, Jeni; Via, Marta; Vodička, Petr; Zhang, Yunjiang; Zografou, Olga; Daellenbach, Kaspar Rudolf; Upadhyay, Abhishek; Chen, Gang I.; Manousakas, Manousos-Ioannis; Haddad, Imad El; Prévôt, André S.H.

It is important to study aerosols and their origins, as they pose various negative health and environmental impacts. In this study, we combined year-long datasets from 15 different countries with Trajectory Statistical Methods (TSMs) for the first time at this comprehensive scale. We found possible source regions and seasonal variations of various particulate matter (PM) components in Europe, including total organic aerosol (OA), biomass burning OA (BBOA), oxygenated OA (OOA), ammonium (NH4), nitrate (NO3), and sulphate (SO4). We found that for all of the studied components, Eastern Europe was among the highest contributors. For NO3, other important source regions were Northern France and the Benelux, while for SO4 there were significant contributions from the Mediterranean region. We also compared our measurement-based model with simulated concentrations of an atmospheric chemistry transport model (CAMx). We observed a satisfactory agreement in regions where we had sufficient coverage with air pollution monitoring stations. The main deviations for OA were found around the Po Valley, where CAMx consistently estimated higher concentrations, while the TSM analysis did not highlight it as a hotspot because long-term monitoring datasets in this region are lacking. CAMx also underestimated the concentrations around Poland, mainly from residential burning. Our results provide opportunities to refine European emission inventories and deliver valuable information on long-range transported air pollutants. This work suggests that policies mitigating air pollution in Eastern Europe and the Benelux could help improve overall air quality in entire Europe more efficiently.

2025

Towards a remote-sensing-driven model of isoprene emissions from Alpine tundra

Westergaard-Nielsen, Andreas; Maigaard, R S; Davie-Martin, Cleo Lisa; Seco, Roger; Holst, T; Pirk, Norbert; Laursen, Simon Nyboe; Rinnan, Riikka

Abstract This study investigates isoprene emissions in a high-latitude Alpine tundra ecosystem, focusing on using near-field remote sensing of surface temperatures, the photochemical reflectance index (PRI) and normalized difference vegetation index (NDVI), and meteorological measurements to model these emissions. Isoprene is a key biogenic volatile organic compound (BVOC) emitted by select plants, which can impact atmospheric chemistry and climate. Increased temperatures, particularly in high latitudes, may enhance isoprene emissions due to extended growing seasons and heightened plant stress. The research was conducted in Finse, Norway, where isoprene and CO 2 fluxes were measured with eddy covariance alongside spectral and meteorological data, and surface temperature. A random forest (RF) model was developed to predict isoprene fluxes, considering the variable importance of different environmental factors. The results showed that surface temperature and CO 2 flux were consistently important predictors, across three differential temporal data aggregations (hourly, daily, weekly), while the PRI demonstrated low predictive power, possibly due to the heterogeneous vegetation and variable light conditions. The NDVI was more effective than anticipated, likely linked to phenological changes in vegetation. Model performance varied with temporal resolution, with weekly data achieving the highest predictive accuracy ( R 2 up to 0.76). The RF model accurately reflected seasonal emission patterns but underestimated short-term peaks, suggesting the potential to combine machine learning with process-based modelling. This research highlights the promise of proxy data from remote sensing for scaling BVOC emission models to regional levels, essential for understanding climate impacts in Arctic ecosystems.

2025

The impact of tropospheric blocking on the duration of the sudden stratospheric warmings in boreal winter 2023/24

Vorobeva, Ekaterina; Orsolini, Yvan

The winter of 2023/24 exhibited remarkable stratospheric dynamics with multiple sudden stratospheric warmings (SSWs). Based on the fifth-generation European Centre for Medium-Range Weather Forecasts (ECMWF) reanalysis (ERA5) polar-cap-averaged 10 hPa zonal wind, three major SSWs are identified. Two of the three SSWs were short-lived, lasting under 7 d. In this study, we give an overview of the three SSWs that occurred in the winter of 2023/24 and focus on the impact of tropospheric forcing on their duration. Blocking high-pressure systems are shown to modulate wave activity flux into the stratosphere through interactions with tropospheric planetary waves, depending on their location. The rapid termination of the first SSW (14–19 January 2024) is linked to a developing high-pressure system over the North Pacific. The second SSW (16–22 February 2024) terminated quickly due to more contributing factors, one of which was a high-pressure system that developed over the Far East. The third SSW (3–28 March 2024) was a long-duration canonical event extending to levels below 100 hPa. In contrast to the two short-lived SSWs in the winter of 2023/24, tropospheric forcing was sustained around the SSW onset in March 2024, allowing a long event to develop. We also note that conditions for these SSWs were particularly favorable due to external factors, including an easterly Quasi-Biennial Oscillation (QBO), the presence of El Niño conditions of the El Niño–Southern Oscillation (ENSO) cycle, and the proximity to the solar maximum.

2025

Scene-to-Scene classification variability in spatiotemporal glacier surface facies mapping in Svalbard

Wankhede, Sagar Filipe; Jolly, Christo; Balakrishna, Keshava; Jawak, Shridhar Digambar

2025

Designing an ethical and explainable automatic coaching (eCoach) system for community based, persuasive recommendations

Chatterjee, Ayan; Riegler, Michael; Halvorsen, Pål

Abstract This study introduces a community-focused eCoach recommendation system aimed at enhancing physical activity by leveraging demographic data, wearable sensor inputs, and machine learning algorithms to generate both individual and community-based activity recommendations using advice-based collaborative filtering. Existing eCoaching systems largely focus on personalized feedback without incorporating social reinforcement or group-level motivation, creating a gap in leveraging community influence for sustained health behaviors. Our system combines real-time activity tracking through wearable sensors and advice-based collaborative filtering to deliver adaptive recommendations. We collected data from 31 participants (16 using MOX2-5 sensors and 15 from a public Fitbit-based dataset), targeting daily activity levels to generate actionable guidance. Through decision tree classification and SHAP-based interpretability, we achieved a model accuracy of 99.8%, with F1, precision, recall, and MCC metrics confirming robustness across both balanced and imbalanced datasets. Ethical considerations, including privacy, bias mitigation, and informed consent, were integral to our design and implementation. Limitations include potential biases due to sample size and data imbalances, suggesting the need for future validation on independent datasets. This system demonstrates the potential to integrate with real-world healthcare initiatives, offering trust, transparency, and user engagement opportunities to meet public health objectives.

2025

Cyanobakterier og cyanotoksiner i norske drikkevannskilder - (VKM)

Samdal, Ingunn Anita; Ballot, Andreas Hendrik; Boahene, Nana Yaa; Eriksen, Gunnar Sundstøl; Flø, Daniel; Haande, Sigrid; Svendsen, Camilla; Amlund, Heidi; Beyer, Jonny; Brantsæter, Anne Lise; Bremer, Sara; Mariussen, Espen; Thomsen, Cathrine; Knutsen, Helle Katrine

2021

Estimating surface NO2 concentrations over Europe using Sentinel-5P TROPOMI

Shetty, Shobitha; Schneider, Philipp; Stebel, Kerstin; Hamer, Paul David; Kylling, Arve; Berntsen, Terje Koren

Satellite observations from instruments such as the TROPOspheric Monitoring Instrument (TROPOMI) show significant potential for monitoring the spatiotemporal variability of NO2, however they typically provide vertically integrated measurements over the tropospheric column. In this study, we introduce a machine learning approach entitled ‘S-MESH’ (Satellite and ML-based Estimation of Surface air quality at High resolution) that allows for estimating daily surface NO2 concentrations over Europe at 1 km spatial resolution based on eXtreme gradient boost (XGBoost) model using primarily observation-based datasets over the period 2019–2021. Spatiotemporal datasets used by the model include TROPOMI NO2 tropospheric vertical column density, night light radiance from the Visible Infrared Imaging Radiometer Suite (VIIRS), Normalized Difference Vegetation Index from the Moderate Resolution Imaging Spectroradiometer (MODIS), observations of air quality monitoring stations from the European Environment Agency database and modeled meteorological parameters such as planetary boundary layer height, wind velocity, temperature. The overall model evaluation shows a mean absolute error of 7.77 μg/m3, a median bias of 0.6 μg/m3 and a Spearman rank correlation of 0.66. The model performance is found to be influenced by NO2 concentration levels, with the most reliable predictions at concentration levels of 10–40 μg/m3 with a bias of

2024

Biomass burning emission analysis based on MODIS

Petrenko, Mariya; Kahn, Ralph; Chin, Mian; Bauer, Susanne; Bergman, Tommi; Bian, Huisheng; Curci, Gabriele; Johnson, Ben; Kaiser, Johannes; Kipling, Zak; Kokkola, Harri; Liu, Xiaohong; Mezuman, Keren; Mielonen, Tero; Myhre, Gunnar; Pan, Xiaohua; Protonotariou, Anna; Remy, Samuel; Skeie, Ragnhild Bieltvedt; Stier, Philip; Toshihiko, Takemura; Tsigaridis, Kostas; Wang, Hailong; Watson-Parris, Duncan; Zhang, Kai

We assessed the biomass burning (BB) smoke aerosol optical depth (AOD) simulations of 11 global models that participated in the AeroCom phase III BB emission experiment. By comparing multi-model simulations and satellite observations in the vicinity of fires over 13 regions globally, we (1) assess model-simulated BB AOD performance as an indication of smoke source–strength, (2) identify regions where the common emission dataset used by the models might underestimate or overestimate smoke sources, and (3) assess model diversity and identify underlying causes as much as possible. Using satellite-derived AOD snapshots to constrain source strength works best where BB smoke from active sources dominates background non-BB aerosol, such as in boreal forest regions and over South America and southern hemispheric Africa. The comparison is inconclusive where the total AOD is low, as in many agricultural burning areas, and where the background is high, such as parts of India and China. Many inter-model BB AOD differences can be traced to differences in values for the mass ratio of organic aerosol to organic carbon, the BB aerosol mass extinction efficiency, and the aerosol loss rate from each model. The results point to a need for increased numbers of available BB cases for study in some regions and especially to a need for more extensive regional-to-global-scale measurements of aerosol loss rates and of detailed particle microphysical and optical properties; this would both better constrain models and help distinguish BB from other aerosol types in satellite retrievals. More generally, there is the need for additional efforts at constraining aerosol source strength and other model attributes with multi-platform observations.

2025

A global assemblage of regional prescribed burn records — GlobalRx

Hsu, Alice; Jones, Matthew W.; Thurgood, Jane R.; Smith, Adam J. P.; Carmenta, Rachel; Abatzoglou, John T.; Anderson, Liana O.; Clarke, Hamish; Doerr, Stefan H.; Fernandes, Paulo M.; Kolden, Crystal A.; Santín, Cristina; Strydom, Tercia; Quéré, Corinne Le; Ascoli, Davide; Castellnou, Marc; Goldammer, Johann G.; Guiomar, Nuno Ricardo Gracinhas Nunes; Kukavskaya, Elena A.; Rigolot, Eric; Tanpipat, Veerachai; Varner, Morgan; Yamashita, Youhei; Baard, Johan; Barreto, Ricardo; Becerra, Javier; Brunn, Egbert; Bergius, Niclas; Carlsson, Julia; Cheney, Chad; Druce, Dave; Elliot, Andy; Evans, Jay; Falleiro, Rodrigo De Moraes; Prat-Guitart, Nuria; Hiers, J. Kevin; Kaiser, Johannes; Macher, Lisa; Morris, Dave; Park, Jane; Robles, César; Román-Cuesta, Rosa María; Rücker, Gernot; Senra, Francisco; Steil, Lara; Valverde, Jose Alejandro Lopez; Zerr, Emma

Abstract Prescribed burning (RxB) is a land management tool used widely for reducing wildfire hazard, restoring biodiversity, and managing natural resources. However, RxB can only be carried out safely and effectively under certain seasonal or weather conditions. Under climate change, shifts in the frequency and timing of these weather conditions are expected but analyses of climate change impacts have been restricted to select few regions partly due to a paucity of RxB records at global scale. Here, we introduce GlobalRx, a dataset including 204,517 RxB records from 1979–2023, covering 16 countries and 209 terrestrial ecoregions. For each record, we add a comprehensive suite of meteorological variables that are regularly used in RxB prescriptions by fire management agencies, such as temperature, humidity, and wind speed. We also characterise the environmental setting of each RxB, such as land cover and protected area status. GlobalRx enables the bioclimatic range of conditions suitable for RxB to be defined regionally, thus unlocking new potential to study shifting opportunities for RxB planning and implementation under future climate.

2025

A worldwide aerosol phenomenology: Elemental and organic carbon in PM2.5 and PM10

Putaud, Jean-Philippe; Cavalli, Fabrizia; Yttri, Karl Espen; Chow, Judith C.; Watson, John G.; Sinha, Baerbel; Venkataraman, Chandra; Ikemori, Fumikazu; Jaffrezo, Jean-Luc; Uzu, Gaelle; Moreno, Isabel; Krejci, Radovan; Laj, Paolo; Gupta, Tarun; Hu, Min; Kim, Sang-Woo; Mayol-Bracero, Olga; Quinn, Patricia; Aas, Wenche; Alastuey, Andres; Andrade, Marcos; Angelucci, Monica; Anurag, Gupta; Beukes, J. Paul; Bhardwaj, Ankur; Chatterjee, Abhijit; Chaudhary, Pooja; Chhangani, Anil Kumar; Conil, Sébastien; Degorska, Anna; Devaliya, Sandeep; Dhandapani, Abisheg; Duhan, Sandeep Singh; Dumka, Umesh Chandra; Habib, Gazala; Hamzavi, Zahra; Haswani, Diksha; Herrmann, Hartmut; Holubova, Adela; Hueglin, Christoph; Imran, Mohd; Jehangir, Arshid; Kapoor, Taveen Singh; Karanasiou, Angeliki; Khaiwal, Ravindra; Kim, Jeongeun; Kolesa, Tanja; Kozakiewicz, Joanna; Kranjc, Irena; Laura, Jitender Singh; Lian, Yang; Liu, Junwen; Manwani, Pooja; Mardoñez-Balderrama, Valeria; Marticorena, Béatrice; Matsuki, Atsushi; Mor, Suman; Mukherjee, Sauryadeep; Murthy, Sadashiva; Muthalagu, Akila; Najar, Tanveer Ahmad; Kumar, Radhakrishnan Naresh; Pandithurai, Govindan; Perez, Noemi; Phairuang, Worradorn; Phuleria, Harish C.; Poulain, Laurent; Prasad, Laxmi; Pullokaran, Delwin; Qadri, Adnan Mateen; Qureshi, Asif; Ramírez, Omar; Roy, Sayantee; Rüdiger, Julian; Saikia, Binoy K.; Saikia, Prasenjit; Sauvage, Stéphane; Savvides, Chrysanthos; Sharma, Renuka; Singh, Tanbir; Singh, Gyanesh Kumar; Spoor, Ronald; Srivastava, Atul Kumar; Raman, Ramya Sunder; Zyl, Pieter G. Van; Vecchiocattivi, Marco; Voiron, Céline; Xin, Jinyuan; Yadav, Kajal

Elemental carbon (EC), organic carbon (OC), and particulate matter (PM) concentrations in the inhalable (PM10) and fine (PM2.5) size fractions are measured worldwide, albeit with different analytical methods. These measurements from many researchers were collected and analyzed for Africa, America, Asia, and Europe for 2012–2019. EC/PM, OC/PM, and OC/EC ratios were examined based on region, site type, and season to infer potential sources and impacts. These analyses demonstrate that carbonaceous materials are important PM constituents throughout the world. Mean EC/PM ratios were lowest in PM10 in Sahelian Africa and Europe (∼0.01), highest (>0.07) in PM2.5 at urban sites in North America, South America, and Japan. Mean OC/PM ratios were lowest in PM10 in the Sahel (∼0.06) and in PM2.5 in China and Thailand (0.10), and highest in central and eastern Europe (∼0.3) and North America (∼0.4). OC/EC ratios were elevated in western and northern Europe, and at regional background sites in North America. EC/PM increased with PM10 in Thailand, while OC/PM increased with higher PM mass in Thailand, India, and North America, highlighting the specific contribution of carbonaceous aerosols to PM pollution in these regions. At European and North American background sites, OC/EC ratios increased with PM mass. Higher OC/EC ratios in dry periods indicate influence of wildfires, prescribed burns, and secondary aerosol formation. Elevated wintertime EC/PM ratios coincide with residential heating in temperate climate zones.

2025

DNA damage in oral mucosal epithelial cells cultured in complex and xenobiotic-free media: a comparison study

Cabral, Joao Victor; Vodenkova, Sona; Tomasova, Kristyna; Vodickova, Ludmila; Yamani, Naouale El; Rundén-Pran, Elise; Dusinska, Maria; Safanda, Adam; Jirsova, Katerina

Abstract In this study, we evaluated the genomic stability of oral mucosal epithelial cells (OMECs) cultured in complex media (COM) and xenobiotic-free media (XF) to assess their potential clinical application for limbal stem cell deficiency (LSCD) treatments. OMECs serve as a promising autologous cell source for bilateral LSCD treatment, offering an alternative to limbal epithelial cells (LECs). However, genomic integrity is crucial to ensure the long-term success of transplanted cells. We performed micronucleus (MNi) tests and comet assays to compare DNA damage in OMECs cultured in both media types. The results indicated no significant differences in cell morphology, viability, or size between the two conditions. The MNi frequency was similar, with 5.67 and 6.17 MNi per 1,000 cells in COM and XF conditions, respectively. Comet assay results showed low levels of strand breaks (SBs) and oxidized DNA lesions in both media, with XF showing a slightly lower, albeit statistically insignificant, percentage of tail DNA for net Fpg-sensitive sites. Our findings suggest that OMECs can be effectively cultivated in either COM or XF media without inducing significant DNA damage, supporting the potential use of XF media in clinical settings to reduce contamination risks. This study underscores the importance of genomic stability in cultured cells for ocular surface transplantation, contributing valuable insights into optimizing culture conditions for safer and more effective clinical applications.

2025

Modelling Arctic lower-tropospheric ozone: processes controlling seasonal variations

Gong, Wanmin; Beagley, Stephen R.; Toyota, Kenjiro; Skov, Henrik; Christensen, Jesper Heile; Lupu, Alex; Pendlebury, Diane; Zhang, Junhua; Im, Ulas; Kanaya, Yugo; Saiz-Lopez, Alfonso; Sommariva, Roberto; Effertz, Peter; Halfacre, John W.; Jepsen, Nis; Kivi, Rigel; Koenig, Theodore K.; Müller, Katrin; Nordstrøm, Claus; Petropavlovskikh, Irina; Shepson, Paul B.; Simpson, William R.; Solberg, Sverre; Staebler, Ralf M.; Tarasick, David W.; Malderen, Roeland Van; Vestenius, Mika

Abstract. Previous assessments on modelling Arctic tropospheric ozone (O3) have shown that most atmospheric models continue to experience difficulties in simulating tropospheric O3 in the Arctic, particularly in capturing the seasonal variations at coastal sites, primarily attributed to the lack of representation of surface bromine chemistry in the Arctic. In this study, two independent chemical transport models (CTMs), DEHM (Danish Eulerian Hemispheric Model) and GEM-MACH (Global Environmental Multi-scale – Modelling Air quality and Chemistry), were used to simulate Arctic lower-tropospheric O3 for the year 2015 at considerably higher horizontal resolutions (25 and 15 km, respectively) than the large-scale models in the previous assessments. Both models include bromine chemistry but with different mechanistic representations of bromine sources from snow- and ice-covered polar regions: a blowing-snow bromine source mechanism in DEHM and a snowpack bromine source mechanism in GEM-MACH. Model results were compared with a suite of observations in the Arctic, including hourly observations from surface sites and mobile platforms (buoys and ships) and ozonesonde profiles, to evaluate models' ability to simulate Arctic lower-tropospheric O3, particularly in capturing the seasonal variations and the key processes controlling these variations. Both models are found to behave quite similarly outside the spring period and are able to capture the observed overall surface O3 seasonal cycle and synoptic-scale variabilities, as well as the O3 vertical profiles in the Arctic. GEM-MACH (with the snowpack bromine source mechanism) was able to simulate most of the observed springtime ozone depletion events (ODEs) at the coastal and buoy sites well, while DEHM (with the blowing-snow bromine source mechanism) simulated much fewer ODEs. The present study demonstrates that the springtime O3 depletion process plays a central role in driving the surface O3 seasonal cycle in central Arctic, and that the bromine-mediated ODEs, while occurring most notably within the lowest few hundred metres of air above the Arctic Ocean, can induce a 5 %–7 % of loss in the total pan-Arctic tropospheric O3 burden during springtime. The model simulations also showed an overall enhancement in the pan-Arctic O3 concentration due to northern boreal wildfire emissions in summer 2015; the enhancement is more significant at higher altitudes. Higher O3 excess ratios (ΔO3/ΔCO) found aloft compared to near the surface indicate greater photochemical O3 production efficiency at higher altitudes in fire-impacted air masses. The model simulations further indicated an enhancement in NOy in the Arctic due to wildfires; a large portion of NOy produced from the wildfire emissions is found in the form of PAN that is transported to the Arctic, particularly at higher altitudes, potentially contributing to O3 production there.

2025

Assessment of the impact on biodiversity by using sterile fish in aquaculture

Bodin, Johanna Eva; Hindar, Kjetil; Dalen, Knut Tomas; Duale, Nur; Garseth, Åse Helen; Malmstrøm, Martin; Sipinen, Ville Erling; Thorstad, Eva Bonsak; Velle, Gaute; Berg, Paul Ragnar; Mo, Tor-Atle; Olesen, Ingrid; Olsen, Ann-Karin Hardie; Rimstad, Espen

2025

Opinion of the Scientific Committee on health, environmental and emerging risks on the safety of titanium dioxide in toys

Bodin, Laurent; Dusinska, Maria; Stepnik, Maciej; Wijnhoven, Susan; Autrup, Herman; Goetz, Natalie von; Vermeire, Theo G.; Hoet, Peter; Ion, Rodica Mariana; Krätke, Renate; Proykova, Ana; Scott, Marian; Jong, Wim H. de

The Opinion of the Scientific Committee on Health, Environmental and Emerging Risks advises the European Commission on whether the uses of titanium dioxide in toys and toy materials can be considered to be safe in light of the identified exposure, and the classification of titanium dioxide as carcinogenic category 2 after inhalation. Four toy products including casting kits, chalk, powder paints and white colour pencils containing various amounts of TiO2 as colouring agent were evaluated for inhalation risks. For the oral route, childrens’ lip gloss/lipstick, finger paint and white colour pencils were evaluated.

When it can be demonstrated with high certainty that no ultrafine fraction is present in pigmentary TiO2 preparations used in toys and toy materials, safe use with no or negligible risk for all products considered is indicated based on the exposure estimations of this Opinion. However, if an ultrafine fraction is assumed to be present, safe use is not indicated, except for white colour pencils.

2024

Do cytotoxicity and cell death cause false positive results in the in vitro comet assay?

Azqueta, Amaya; Stopper, Helga; Zegura, Bojana; Dusinska, Maria; Møller, Peter

The comet assay is used to measure DNA damage induced by chemical and physical agents. High concentrations of test agents may cause cytotoxicity or cell death, which may give rise to false positive results in the comet assay. Systematic studies on genotoxins and cytotoxins (i.e. non-genotoxic poisons) have attempted to establish a threshold of cytotoxicity or cell death by which DNA damage results measured by the comet assay could be regarded as a false positive result. Thresholds of cytotoxicity/cell death range from 20% to 50% in various publications. Curiously, a survey of the latest literature on comet assay results from cell culture studies suggests that one-third of publications did not assess cytotoxicity or cell death. We recommend that it should be mandatory to include results from at least one type of assay on cytotoxicity, cell death or cell proliferation in publications on comet assay results. A combination of cytotoxicity (or cell death) and proliferation (or colony forming efficiency assay) is preferable in actively proliferating cells because it covers more mechanisms of action. Applying a general threshold of cytotoxicity/cell death to all types of agents may not be applicable; however, 25% compared to the concurrent negative control seems to be a good starting value to avoid false positive comet assay results. Further research is needed to establish a threshold value to distinguish between true and potentially false positive genotoxic effects detected by the comet assay.

2022

Volatile Organic Compounds of Diverse Origins and Their Changes Associated With Cultivar Decay in a Fungus-Farming Termite

Vidkjær, Nanna Hjort; Schmidt, Suzanne; Davie-Martin, Cleo Lisa; Silué, Kolotchèlèma Simon; Koné, N'golo Abdoulaye; Rinnan, Riikka; Poulsen, Michael

Fungus-farming termites cultivate a Termitomyces fungus monoculture in enclosed gardens (combs) free of other fungi, except during colony declines, where Pseudoxylaria spp. stowaway fungi appear and take over combs. Here, we determined Volatile Organic Compounds (VOCs) of healthy Macrotermes bellicosus nests in nature and VOC changes associated with comb decay during Pseudoxylaria takeover. We identified 443 VOCs and unique volatilomes across samples and nest volatilomes that were mainly composed of fungus comb VOCs with termite contributions. Few comb VOCs were linked to chemical changes during decay, but longipinocarvone and longiverbenone were only emitted during comb decay. These terpenes may be involved in Termitomyces defence against antagonistic fungi or in fungus-termite signalling of comb state. Both comb and Pseudoxylaria biomass volatilomes contained many VOCs with antimicrobial activity that may serve in maintaining healthy Termitomyces monocultures or aid in the antagonistic takeover by Pseudoxylaria during colony decline. We further observed a series of oxylipins with known functions in the regulation of fungus germination, growth, and secondary metabolite production. Our volatilome map of the fungus-farming termite symbiosis provides new insights into the chemistry regulating complex interactions and serves as a valuable guide for future work on the roles of VOCs in symbioses.

2025

Very Strong Atmospheric Methane Growth in the 4 Years 2014-2017: Implications for the Paris Agreement

Nisbet, E. G.; Manning, M. R.; Dlugokencky, E. J.; Fisher, R. E.; Lowry, D.; Michel, S. E.; Myhre, Cathrine Lund; Platt, Stephen Matthew; Allen, G.; Bousquet, P.; Brownlow, R.; Cain, M.; France, J. L.; Hermansen, Ove; Hossaini, R.; Jones, A. E.; Levin, I.; Manning, A. C.; Myhre, Gunnar; Pyle, J. A.; Vaughn, B.; Warwick, N. J.; White, James W. C.

Atmospheric methane grew very rapidly in 2014 (12.7 ± 0.5 ppb/year), 2015 (10.1 ± 0.7 ppb/year), 2016 (7.0 ± 0.7 ppb/year), and 2017 (7.7 ± 0.7 ppb/year), at rates not observed since the 1980s. The increase in the methane burden began in 2007, with the mean global mole fraction in remote surface background air rising from about 1,775 ppb in 2006 to 1,850 ppb in 2017. Simultaneously the 13C/12C isotopic ratio (expressed as δ13CCH4) has shifted, has shifted, now trending negative for more than a decade. The causes of methane's recent mole fraction increase are therefore either a change in the relative proportions (and totals) of emissions from biogenic and thermogenic and pyrogenic sources, especially in the tropics and subtropics, or a decline in the atmospheric sink of methane, or both. Unfortunately, with limited measurement data sets, it is not currently possible to be more definitive. The climate warming impact of the observed methane increase over the past decade, if continued at >5 ppb/year in the coming decades, is sufficient to challenge the Paris Agreement, which requires sharp cuts in the atmospheric methane burden. However, anthropogenic methane emissions are relatively very large and thus offer attractive targets for rapid reduction, which are essential if the Paris Agreement aims are to be attained.
PLAIN LANGUAGE SUMMARY: The rise in atmospheric methane (CH4), which began in 2007, accelerated in the past 4 years. The growth has been worldwide, especially in the tropics and northern midlatitudes. With the rise has come a shift in the carbon isotope ratio of the methane. The causes of the rise are not fully understood, and may include increased emissions and perhaps a decline in the destruction of methane in the air. Methane's increase since 2007 was not expected in future greenhouse gas scenarios compliant with the targets of the Paris Agreement, and if the increase continues at the same rates it may become very difficult to meet the Paris goals. There is now urgent need to reduce methane emissions, especially from the fossil fuel industry.

2019

Effects of extreme meteorological conditions in 2018 on European methane emissions estimated using atmospheric inversions

Thompson, Rona Louise; Zwaaftink, Christine Groot; Brunner, D; Tsuruta, Aki; Aalto, T; Raivonen, M; Crippa, M.; Solazzo, Efisio; Guizzardi, D.; Regnier, P.; Maisonnier, M.

The effect of the 2018 extreme meteorological conditions in Europe on methane (CH4) emissions is examined using estimates from four atmospheric inversions calculated for the period 2005–2018. For most of Europe, we find no anomaly in 2018 compared to the 2005–2018 mean. However, we find a positive anomaly for the Netherlands in April, which coincided with positive temperature and soil moisture anomalies suggesting an increase in biogenic sources. We also find a negative anomaly for the Netherlands for September–October, which coincided with a negative anomaly in soil moisture, suggesting a decrease in soil sources. In addition, we find a positive anomaly for Serbia in spring, summer and autumn, which coincided with increases in temperature and soil moisture, again suggestive of changes in biogenic sources, and the annual emission for 2018 was 33 ± 38% higher than the 2005–2017 mean. These results indicate that CH4 emissions from areas where the natural source is thought to be relatively small can still vary due to meteorological conditions. At the European scale though, the degree of variability over 2005–2018 was small, and there was negligible impact on the annual CH4 emissions in 2018 despite the extreme meteorological conditions.

This article is part of a discussion meeting issue ‘Rising methane: is warming feeding warming? (part 2)’.

2021

2000 years of climate, environmental, and societal variability in southeastern Norway from the annually laminated sediments of Lake Sagtjernet

Ballo, Eirik Gottschalk; D’Andrea, William J.; Høeg, Helge Irgens; Loftsgarden, Kjetil; Bajard, Manon Juliette Andree; Eckhardt, Sabine; Cassiani, Massimo; Evangeliou, Nikolaos; Bakke, Jostein; Krüger, Kirstin

2025

Elucidation of contamination sources for poly- and perfluoroalkyl substances (PFASs) on Svalbard (Norwegian Arctic)

Skaar, Jøran Solnes; Ræder, Erik Magnus; Lyche, Jan Ludvig; Ahrens, Lutz; Kallenborn, Roland

A combination of local (i.e. firefighting training facilities) and remote sources (i.e., long-range transport) are assumed to be responsible for the occurrence of per- and polyfluoroalkyl substances (PFASs) in Svalbard (Norwegian Arctic). However, no systematic elucidation of local PFASs sources have been conducted yet. Therefore, a survey was performed aiming at identifying local PFASs pollution sources on the island of Spitsbergen (Svalbard, Norway). Soil, fresh water (lake, draining rivers), sea water, melt-water run-off, surface snow and coastal sediment samples were collected from Longyearbyen (Norwegian mining town), Ny-Ålesund (research facility) and the Lake Linnévatnet area (background site) during several campaigns (2014-2016) and analysed for 14 individual target PFASs. For background site (Linnévatnet area, sampling during April to June 2015), ∑PFAS levels ranged from 0.4 – 4 ng/L in surface lake water (n = 20). PFAS in melt water from the contributing glaciers showed similar concentrations (~4 ng/L, n = 2). The short chain perfluorobutanoate (PFBA) was predominant in lake water (60-80% of the ∑PFASs), meltwater (20-30 %) and run-off water (40 %). Long range transport is assumed to be the major PFAS source. In Longyearbyen, 5 water samples (i.e. 2 seawater, 3 run-off) were collected near the local firefighting training site (FFTS) in November 2014 and June 2015, respectively. The highest PFAS levels were found in FFTS melt water run-off (118 ng/L). PFOS was the most abundant compound in the FFTS meltwater run-off (53 – 58 % PFASs). At the research station Ny-Ålesund, sea water (n = 6), soil (n = 9) and fresh water (n = 10) were collected in June 2016. Low ∑PFAS concentrations were determined for sea water (5 - 6 ng/L), whereas high ∑PFAS concentrations were found in run-off water (113 – 119 ng/L) and soil (211 – 800 ng/g dry weight (dw)) collected close to the local FFTS. In addition, high ∑PFAS levels (127 ng/L) were also found in fresh water from lake Solvatnet close to former sewage treatment facility. Overall, at both FFTS affected sites (soil, water), PFOS was the most abundant compound (60 – 69% of ∑PFASs). FFTS and landfill locations were identified as major PFASs sources for Svalbard settlements.

2018

Seasonality of the particle number concentration and size distribution: a global analysis retrieved from the network of Global Atmosphere Watch (GAW) near-surface observatories

Rose, Clemence; Coen, Martine Collaud; Andrews, Elisabeth; Lin, Yong; Bossert, Isaline; Myhre, Cathrine Lund; Tuch, Thomas; Wiedensohler, Alfred; Fiebig, Markus; Aalto, Pasi; Alastuey, Andrés; Alonso-Blanco, Elisabeth; Andrade, Marcos; Artiñano, Begoña; Arsov, Todor; Baltensprenger, Urs; Bastian, Susanne; Bath, Olaf; Beukes, Johan Paul; Brem, Benjamin T.; Bukowiecki, Nicolas; Casquero-Vera, Juan Andres; Conil, Sébastien; Eleftheriadis, Konstantinos; Favez, Olivier; Flentje, Harald; Gini, Maria I.; Gómez-Moreno, Francisco Javier; Gysel-Beer, Martin; Hallar, Anna Gannet; Kalapov, Ivo; Kalivitis, Nikos; Kasper-Giebl, Anne; Keywood, Melita; Kim, Jeong Eun; Kim, Sang-Woo; Kristensson, Adam; Kulmala, Markku; Lihavainen, Heikki; Lin, Neng-Huei; Lyamani, Hassan; Marinoni, Angela; Santos, Sebastiao Martins Dos; Mayol-Bracero, Olga; Meinhardt, Frank; Merkel, Maik; Metzger, Jean-Marc; Mihalopoulos, Nikolaos; Ondráček, Jakub; Pandolfi, Marco; Pérez, Noemi; Petäjä, Tuukka; Petit, Jean-Eudes; Picard, David; Pichon, Jean-Marc; Pont, Veronique; Putaud, Jean-Philippe; Reisen, Fabienne; Sellegri, Karine; Sharma, Sangeeta; Schauer, Gerhard; Sheridan, Patrick; Sherman, James Patrick; Schwerin, Andreas; Sohmer, Ralf; Sorribas, Mar; Sun, Junying; Tulet, Pierre; Vakkari, Ville; Zyl, Pieter Gideon van; Velarde, Fernando; Villani, Paolo; Vratolis, Stergios; Wagner, Zdenek; Wang, Sheng-Hsiang; Weinhold, Kay; Weller, Rolf; Yela, Margarita; Ždímal, Vladimir; Laj, Paolo G.

Aerosol particles are a complex component of the atmospheric system which influence climate directly by interacting with solar radiation, and indirectly by contributing to cloud formation. The variety of their sources, as well as the multiple transformations they may undergo during their transport (including wet and dry deposition), result in significant spatial and temporal variability of their properties. Documenting this variability is essential to provide a proper representation of aerosols and cloud condensation nuclei (CCN) in climate models. Using measurements conducted in 2016 or 2017 at 62 ground-based stations around the world, this study provides the most up-to-date picture of the spatial distribution of particle number concentration (Ntot) and number size distribution (PNSD, from 39 sites). A sensitivity study was first performed to assess the impact of data availability on Ntot's annual and seasonal statistics, as well as on the analysis of its diel cycle. Thresholds of 50 % and 60 % were set at the seasonal and annual scale, respectively, for the study of the corresponding statistics, and a slightly higher coverage (75 %) was required to document the diel cycle.

Although some observations are common to a majority of sites, the variety of environments characterizing these stations made it possible to highlight contrasting findings, which, among other factors, seem to be significantly related to the level of anthropogenic influence. The concentrations measured at polar sites are the lowest (∼ 102 cm−3) and show a clear seasonality, which is also visible in the shape of the PNSD, while diel cycles are in general less evident, due notably to the absence of a regular day–night cycle in some seasons. In contrast, the concentrations characteristic of urban environments are the highest (∼ 103–104 cm−3) and do not show pronounced seasonal variations, whereas diel cycles tend to be very regular over the year at these stations. The remaining sites, including mountain and non-urban continental and coastal stations, do not exhibit as obvious common behaviour as polar and urban sites and display, on average, intermediate Ntot (∼ 102–103 cm−3). Particle concentrations measured at mountain sites, however, are generally lower compared to nearby lowland sites, and tend to exhibit somewhat more pronounced seasonal variations as a likely result of the strong impact of the atmospheric boundary layer (ABL) influence in connection with the topography of the sites. ABL dynamics also likely contribute to the diel cycle of Ntot observed at these stations. Based on available PNSD measurements, CCN-sized particles (considered here as either >50 nm or >100 nm) can represent from a few percent to almost all of Ntot, corresponding to seasonal medians on the order of ∼ 10 to 1000 cm−3, with seasonal patterns and a hierarchy of the site types broadly similar to those observed for Ntot.

Overall, this work illustrates the importance of in situ measurements, in particular for the study of aerosol physical properties, and thus strongly supports the development of a broad global network of near surface observatories to increase and homogenize the spatial coverage of the measurements, and guarantee as well data availability and quality. The results of this study also provide a valuable, freely available and easy to use support for model comparison and validation, with the ultimate goal of contributing to improvement of the representation of aerosol–cloud interactions in models, and, therefore, of the evaluation of the impact of aerosol particles on climate.

2021

The consolidated European synthesis of CH4 and N2O emissions for the European Union and United Kingdom: 1990–2019

Petrescu, Ana Maria Roxana; Qiu, Chunjing; McGrath, Matthew J; Peylin, Philippe; Peters, Glen Philip; Ciais, Philippe; Thompson, Rona Louise; Tsuruta, Aki; Brunner, Dominik; Kuhnert, Matthias; Matthews, Bradley; Palmer, Paul I.; Tarasova, Oksana; Regnier, Pierre; Lauerwald, Ronny; Bastviken, David; Hoglund-Isaksson, Lena; Winiwarter, Wilfried; Etiope, Giuseppe; Aalto, Tuula; Balsamo, Gianpaolo; Bastrikov, Vladislav; Berchet, Antoine; Brockmann, Patrick; Ciotoli, Giancarlo; Conchedda, Giulia; Monica, Crippa; Dentener, Frank; Zwaaftink, Christine Groot; Guizzardi, Diego; Günther, Dirk; Haussaire, Jean-Matthieu; Houweling, Sander; Janssens-Maenhout, Greet; Kouyate, Massaer; Leip, Adrian; Leppänen, Antti; Lugato, Emanuele; Maisonnier, Manon; Manning, Alistair J.; Markkanen, Tiina; McNorton, Joe; Muntean, Marilena; Oreggioni, Gabriel David; Patra, Prabir K.; Perugini, Lucia; Pison, Isabelle; Raivonen, Maarit T.; Saunois, Marielle; Segers, Arjo J.S.; Smith, Pete; Solazzo, Efisio; Tian, Hanqin; Tubiello, Francesco N.; Vesala, Timo; Werf, Guido R. Van Der; Wilson, Chris; Zaehle, Sönke

Knowledge of the spatial distribution of the fluxes of greenhouse gases (GHGs) and their temporal variability as well as flux attribution to natural and anthropogenic processes is essential to monitoring the progress in mitigating anthropogenic emissions under the Paris Agreement and to inform its global stocktake. This study provides a consolidated synthesis of CH4 and N2O emissions using bottom-up (BU) and top-down (TD) approaches for the European Union and UK (EU27 + UK) and updates earlier syntheses (Petrescu et al., 2020, 2021). The work integrates updated emission inventory data, process-based model results, data-driven sector model results and inverse modeling estimates, and it extends the previous period of 1990–2017 to 2019. BU and TD products are compared with European national greenhouse gas inventories (NGHGIs) reported by parties under the United Nations Framework Convention on Climate Change (UNFCCC) in 2021. Uncertainties in NGHGIs, as reported to the UNFCCC by the EU and its member states, are also included in the synthesis. Variations in estimates produced with other methods, such as atmospheric inversion models (TD) or spatially disaggregated inventory datasets (BU), arise from diverse sources including within-model uncertainty related to parameterization as well as structural differences between models. By comparing NGHGIs with other approaches, the activities included are a key source of bias between estimates, e.g., anthropogenic and natural fluxes, which in atmospheric inversions are sensitive to the prior geospatial distribution of emissions. ...

2023

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