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Found 10359 publications. Showing page 396 of 415:

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Skogens helsetilstand i Norge. Resultater fra skogskadeovervåkingen i 2024

Timmermann, Volkmar; Antzée-Hyllseth, Henrik; Børja, Isabella; Clarke, Nicholas; Gohli, Jostein; Krokene, Paal; Kuehne, Christian; Kvamme, Torstein; Meissner, Helge Rainer; Nagy, Nina Elisabeth; Næss, Ole Jakob Bae; Romeiro, Joyce Machado Nunes; Solberg, Sverre; Svensson, Arvid; Økland, Bjørn; Aas, Wenche

Skog dekker nærmere 40 % av Norges landareal. Skogene bidrar til karbonbinding både over og under bakken, forsyner oss med råvarer, spiller en viktig rolle for friluftslivet og er leveområdet for utallige arter. Skogens viktige rolle som leverandør av slike økosystemtjenester forutsetter imidlertid et intakt skogøkosystem, en god skoghelse og en langsiktig og bærekraftig forvaltning.
Skogens helsetilstand påvirkes i stor grad av klima og værforhold, enten direkte ved tørke, frost, snø og vind, eller indirekte ved at klimaet påvirker omfanget og spredningen av soppsykdommer og insektangrep.
Klimaendringene og den forventede økningen i klimarelaterte skogskader gir store utfordringer for forvaltningen av framtidas skogressurser. Det samme gjør invaderende skadegjørere, både allerede etablerte arter og nye som kan komme til Norge i nær framtid. Uansett hvilke utfordringer skogen står overfor, er det viktig med langsiktige skogovervåkingsprogrammer for å kunne oppdage endringer og iverksette tiltak mot truslene. I denne rapporten presenteres resultater fra skogskadeovervåkingen i Norge i 2024 og trender over tid for følgende temaer:
1. Landsrepresentativ skogovervåking;
2. Intensiv skogovervåking;
3. Barkbilleovervåkingen 2024: Fortsatt høye fangster i stormrammede områder;
4. Overvåking av fremmede trelevende insekter;
5. Almesyken sprer seg til nye områder;
6. Overvåking av askas naturlige foryngelse i skog angrepet av askeskuddsyke;
7. Andre spesielle skogskader i 2024.

NIBIO

2025

ArtBio AS i Forskningsparken, Oslo. Spredningsberegninger Rn-220

Berglen, Tore Flatlandsmo; Weydahl, Torleif; Grythe, Henrik

NILU

2025

EMEP-CCC: Progress of work

Aas, Wenche; Tørseth, Kjetil

2025

Assessing the disease burden from air pollution in Europe 2022 - Insights from the ETC HE and EEA

Kienzler, Sarah; Wintermeyer, Dirk; Soares, Joana; Ortiz, Alberto González; Gsella, Artur; Horálek, Jan; Plass, Dietrich

2025

Methane in Svalbard (SvalGaSess)

Hodson, Andrew; Kleber, Gabrielle Emma; Platt, Stephen Matthew; Kalenitchenko, Dimitri Stanislas Desire; Hensgens, Geert; Irvine-Fynn, Tristram; Senger, Kim; Tveit, Alexander Tøsdal; Øvreås, Lise; Hietbrink, Sophie ten; Hollander, Jamie; Ammerlaan, Fenna; Damm, Ellen; Römer, Miriam; Fransson, Agneta; Chierici, Melissa; Delpech, Lisa-Marie; Pirk, Norbert; Sen, Arunima; Redecker, Kelly

Methane is a powerful greenhouse gas whose emission into the atmosphere from Arctic environments is increasing in response to climate change. At present, the increase in atmospheric methane concentrations recorded at Ny-Ålesund and globally threatens the Paris Agreement goal of limiting warming to 2 degrees, preferably 1.5 degrees, by increasing the need for abatements. However, our understanding of the physical, chemical and biological processes that control methane in the Arctic are strongly biased towards just a few lowland sites that are not at all like Svalbard and other similar mountainous, ice-covered regions. Svalbard can therefore be used to better understand these locations. Svalbard’s methane stocks include vast reserves of ancient, geogenic methane trapped beneath glaciers and permafrost. This methane supplements the younger, microbial methane mostly produced in waterlogged soils and wetlands during the summer and early winter. Knowledge about the production, removal and migration of these two methane sources in Svalbard’s complex landscapes and coastal environments has grown rapidly in recent years. However, the need to exploit this knowledge to produce reliable estimates of present-day and future emissions of methane from across the Svalbard landscape is now paramount. This is because understanding these quantities is absolutely necessary when we seek to define how society must adjust in order to better manage greenhouse gases in Earth’s atmosphere

2025

Klatresko bidreg til forureining

Hak, Claudia (interview subject); Kleiven, Maria Fimreite (journalist)

2025

The GreenEO Project: Satellite-Based Services to Support Sustainable Land Use Practices Under the European Green Deal

Hamer, Paul David; Frohn, Lise Marie; Geels, Camilla; Christensen, Jesper; Denby, Bruce; Simpson, David; Hutchings, Nicholas; Lopez-Aparicio, Susana; Schneider, Philipp; Cao, Tuan-Vu; Jimenez, Isadora; Fontenelle, Thais; A, Ronald Van Der; Mijling, Bas; Ding, Jieying; Trigo, Isabel F.; Calvet, Jean-Christophe; Schante, Joanne; Judes, Thomas; Tarrasón, Leonor

2025

EO-based Downscaling for Urban-Scale Air Quality Applications

Schneider, Philipp; Shetty, Shobitha; Hamer, Paul David; Stebel, Kerstin; Kylling, Arve; Hassani, Amirhossein; Berntsen, Terje Koren; Grythe, Henrik; Lopez-Aparicio, Susana; Vallejo, Islen; Weydahl, Torleif; Markelj, Miha

2025

Removal Processes of the Stratospheric SO2 Volcanic Plume From the 2015 Calbuco Eruption

Baray, J.‐L.; Gheusi, F.; Duflot, Valentin; Tulet, P.

Abstract We analyze the volcanic plume from the April 2015 Calbuco eruption over a 35‐day period using simulations from Meso‐NH, a non‐hydrostatic mesoscale atmospheric model. A dedicated parameterization of the deep injection of the plume into the stratosphere ensures a realistic representation when compared to Infrared Atmospheric Sounding Interferometer satellite observations. During the first 12 hr of the eruption, on 22 April 2015, SO 2 mixing ratio reached 29 ppmv between 15 and 18 km for the first eruption pulse, and 38 ppmv between 12 and 16 km for the second. Most SO 2 was injected directly into the stratosphere, with a stratospheric load reaching 308 ktS (kilotons of atomic sulfur, i.e. 616 kilotons of SO 2 ) after the eruption. After 1 month, both stratospheric and tropospheric SO 2 loads returned to near‐background levels. During analysis, the chemical conversion of SO 2 into H 2 SO 4 removed a part of SO 2 from the stratosphere. During the long‐range advection, the co‐location between the subtropical jet stream and the Calbuco plume led to three significant stratospheric intrusions on 24, 26 and 28 April 2015. These events transferred stratospheric SO 2 into the troposphere, SO 2 mixing ratios in the upper troposphere reaching 15 ppmv, 26 and 15 ppbv, respectively. SO 2 is gradually oxidized into H 2 SO 4 , with up to 5 ktS of gaseous H 2 SO 4 in the stratosphere on 30 April, but dynamical processes dominate the SO 2 atmospheric budget over chemical transformations. This study demonstrates that stratospheric intrusions can play a critical role in the removal of volcanic material from the stratosphere following a major eruption.

2025

Daily high-resolution PM2.5 estimation in Europe via ML-based downscaling of CAMS

Schneider, Philipp; Shetty, Shobitha; Stebel, Kerstin; Hamer, Paul David; Hassani, Amirhossein; Salamalikis, Vasileios; Castell, Nuria; Berntsen, Terje Koren

2025

Extremt varmt i stan? Köp en vit bil

Muri, Helene (interview subject)

Global uppvärmning och extremvärme i städerna är ett växande problem. Nu lanserar forskarna en ny och helt oväntad lösning.

2025

Evaluation of EarthCARE radiation products

Svendby, Tove Marit; Gressløs, Benjamin; Sollum, Espen; Stebel, Kerstin; Fjæraa, Ann Mari

2025

Snow DUMP-ing: Direct TD-GC-MS for the analysis of urban snow pollution

Davie-Martin, Cleo Lisa; Pedersen, Kristine B.; Normann, Anne Katrine; Håland, Alexander; Calder, Hannah

2025

Investigating the impact of climate change on PCB-153 exposure in Arctic seabirds with the nested exposure model

Skogeng, Lovise Pedersen; Blévin, Pierre; Breivik, Knut; Bustnes, Jan Ove; Eulaers, Igor; Sagerup, Kjetil; Krogseth, Ingjerd Sunde

At the same time Arctic ecosystems experiences rapid climate change, at a rate four times faster than the global average, they remain burdened by long-range transported pollution, notably with legacy polychlorinated biphenyls (PCBs). The present study investigates the potential impact of climate change on seabird exposure to PCB-153 using the established Nested Exposure Model (NEM), here expanded with three seabird species, i.e. common eider (Somateria mollissima), black-legged kittiwake (Rissa tridactyla) and glaucous gull (Larus hyperboreus), as well as the filter feeder blue mussel (Mytulis edulis). The model's performance was evaluated using empirical time trends of the seabird species in Kongsfjorden, Svalbard, and using tissue concentrations from filter feeders along the northern Norwegian coast. NEM successfully replicated empirical PCB-153 concentrations, confirming its ability to simulate PCB-153 bioaccumulation in the studied seabird species within an order of magnitude. Based on global PCB-153 emission estimates, simulations run until the year 2100 predicted seabird blood concentrations 99% lower than in year 2000. Model scenarios with climate change-induced altered dietary composition and lipid dynamics showed to have minimal impact on future PCB-153 exposure, compared to temporal changes in primary emissions of PCB-153. The present study suggests the potential of mechanistic modelling in assessing POP exposure in Arctic seabirds within a multiple stressor context.

2025

FILTER: Framework for Improving Low-Cost Sensor Network Data for Air Quality Monitoring

Hassani, Amirhossein; Salamalikis, Vasileios; Schneider, Philipp; Stebel, Kerstin; Castell, Nuria

2025

Sources of ultrafine particles at a rural midland site in Switzerland

Dada, Lubna; Brem, Benjamin T.; Amarandi-Netedu, Lidia-Marta; Coen, Martine Collaud; Evangeliou, Nikolaos; Hueglin, Christoph; Nowak, Nora; Modini, Robin L.; Steinbacher, Martin; Gysel-Beer, Martin

Ultrafine particles (UFPs; i.e., atmospheric aerosol particles smaller than 100 nm in diameter) are known to be responsible for a series of adverse health effects as they can deposit in humans' bodies. So far, most field campaigns studying the sources of UFPs have focused on urban environments. This study investigates the outdoor sources of UFPs at the atmospheric monitoring station in Payerne, which represents a typical rural location in Switzerland. We aim to quantify the primary and secondary fractions of UFPs based on specific measurements between July 2020 and July 2021 complementing a series of operational meteorological, trace gas and in situ aerosol observations. To distinguish between primary and secondary contributions, we use a method that relies on measuring the fraction of non-volatile particles as a proxy for primary particles. We further compare our measurement results to previously established methods. We find that primary particles resulting from traffic and residential wood burning (direct emissions – mostly non-volatile BC-rich) contribute less than 40 % to the total number of UFPs, mostly in the Aitken mode. On the other hand, we observe local new particle formation (NPF) events (observed from ∼ 1 nm) evident from the increase in cluster ions (1.5–3 nm) and nucleation-mode particle (2.5–25 nm) concentrations, especially in spring and summer. These events, mediated by sulfuric acid, contribute to increasing the UFP number concentration, especially in the nucleation mode. Besides NPF, the chemical processing of particles emitted from multiple sources (including traffic and residential wood burning) contributes substantially to the nucleation-mode particle concentration. Under the present conditions investigated here, we find that secondary processes mediate the increase in UFP concentration to levels equivalent to those in urban locations, affecting both air quality and human health.

2025

Fate, sources and pathways of chemicals of emerging concern (CECs) in coastal waters

Kallenborn, Roland; Ali, Aasim; Hartz, William Frederik; Zhang, Zi-Feng; Li, Yifan

2025

Matemballasje: Røyter som en Golden Retriever

Schmidt, Natascha (interview subject); Kjellgren, Daniel (journalist)

2025

Screening Program 2024. Substances in electronic waste facilities and wastewater treatment

Nipen, Maja; Wolf, Raoul; Sørmo, Erlend; Rostkowski, Pawel; Vogelsang, Christian; Langberg, Håkon Austad; Beylich, Bjørnar; Nikiforov, Vladimir; Harju, Mikael; Halse, Anne Karine; Borgen, Anders

The 2024 Screening Programme investigated emerging and legacy contaminants in e-waste facilities and wastewater treatment. LCD substances, flame retardants, plasticizers, and their metabolites were found in air, dust, and water near e-waste sites. Bisphenol-related compounds and follow-up substances were detected in wastewater, particularly in sludge and particles. The findings highlight environmental dispersion, treatment efficiency, and the need for continued monitoring.

NILU

2025

Modelling atmospheric transport of aerosol

Eckhardt, Sabine; Evangeliou, Nikolaos

2025

Oceans in danger! EU warns ocean carbon removal once seen as a ‘miracle climate cure’ may turn into a global threat | World News - The Times of India

Muri, Helene

Rest of World News: Ocean carbon removal, touted as a climate solution, faces significant hurdles. A new EU report cautions that these unproven technologies lack evidence

2025

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