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Found 9746 publications. Showing page 375 of 390:

Publication  
Year  
Category

Unprecedented wildfire impact on black and organic carbon in the Western Siberian Arctic

Popovicheva, Olga; Evangeliou, Nikolaos; Chichaeva, M.; Semenova, A.; Kobelev, V.; Czech, H.; Schneider, E.; Rüger, C. P.; Zimmermann, R.; Kasimov, N.

2023

Unprecedented wildfire impact on the Siberian Arctic

Popovicheva, Olga; Chichaeva, Marina; Kobelev, Vasilii; Czech, Hendryk; Schneider, Erik; Schnelle-Kreis, Jürgen; Rüger, Christopher P.; Zimmermann, Ralf; Evangeliou, Nikolaos; Kasimov, Nikolay

2022

Update and improvement of dispersion calculations for emissions to air from TCM's amine plant. Part II-Likely case nitrosamines, nitramines and formaldehyde. NILU OR

Tønnesen, D.

Inert dispersion of a unitary emission has been combined with time dependent air chemistry to provide maximum impact of nitrosamines and nitramines in air and water for emissions from the amine absorber at TCM. The calculations show that likely case impact of nitrosamines and nitramines in air is less than 2 % of the recommended guideline value. The maximum concentrations in fresh water range from0.6 % to 3.2 % of the guideline depending on the use of absorbent and flue gas. The likely case impact show that air concentrations are a factor of 3 to 4 lower than the worst case, while water concentrations are be a factor from 16 to 22 lower than the worst case depending on the type of absorbent.

2011

Update and improvement of dispersion calculations for emissions to air from TCM's amine plant. Part l-Worst case nitrosamines and nitramines. NILU OR

Tønnesen, D.

Inert dispersion of a unitary emission has been combined with time dependent air chemistry to provide maximum impact of nitrosamines and nitramines in air and water for emissions from the amine absorber at TCM. The calculations show that worst case impact of nitrosamines and nitramines in air is 5 % of the recommended guideline value. The maximum concentrations in fresh water range from13 % to 53 % of the guideline depending on the use of absorbent and flue gas. Estimates for a likely case impact show that air concentrations will be a factor of 3 lower than the worst case, while water concentrations will be a factor from 10 to 20 lower than the worst case depending on the type of absorber.

2011

Update of background concentrations over Norway. NILU OR

Schneider, P.; Tønnesen, D.; Denby, B.

A methodology for creating a new dataset of estimated background concentrations of NO2, O3, PM10, and PM2.5 that are representative of a typical year over Norway, was developed. The dataset has a spatial resolution of 10 km × 10 km and an hourly temporal resolution. The methodology is based on a spatial mapping component for obtaining information on annual mean background concentrations, and a temporal characterization component, which uses long-term time series of station data to describe the typical development of background concentrations throughout a day and a year. When combined, these two components allow estimates of typical background concentrations at any time of the year at any location in Norway. Whereas the previously used VLUFT method of 1993 only provided spatially constant data at the county level, the new method presented here provides spatially continuous data at a comparatively high spatial resolution. Furthermore, while the previous method only gave a range of constant values that were considered valid throughout the entire year, the new technique provides continuous time series for a typical year at hourly resolution at any location in Norway.

2011

Update on Polar Ozone: Past, Present, and Future. WMO Global Ozone Research and Monitoring Project, Report No. 55

Dameris, M., Godin-Beekmann, S. (Lead Authors), Alexander, S.; Braesicke, P.; Chipperfield, M.; de Laat, A.T.J.; Orsolini, Y.; Rex,M.; Santee, M.L.

2014

Updated environmental assessment of the regional impact from the oil activity in the North Sea. Regular atmospheric emissions - consequences. NILU OR

Knudsen, S.; Solberg, S.; Wathne, B.M.; Høgåsen, T.; Magnusson, J.; Tollefsen, K.E.; Aarrestad, P.A.; Reitan, O.; Stebel, K.; Walker, S.E.

The Report updates the effects of emissions to air of nitrogenoxides and PAH from the offshore industry in the North sea. The report is a part of the updating of the consequence analysis in 1999.

2006

Updated trends for atmospheric mercury in the Arctic: 1995–2018

MacSween, Katrina; Stupple, Geoff; Aas, Wenche; Kyllönen, Katriina; Pfaffhuber, Katrine Aspmo; Skov, Henrik; Steffen, Alexandra; Berg, Torunn; Mastromonaco, Michelle Nerentorp

The Arctic region forms a unique environment with specific physical, chemical, and biological processes affecting mercury (Hg) cycles and limited anthropogenic Hg sources. However, historic global emissions and long range atmospheric transport has led to elevated Hg in Arctic wildlife and waterways. Continuous atmospheric Hg measurements, spanning 20 years, and increased monitoring sites has allowed a more comprehensive understanding of how Arctic atmospheric mercury is changing over time. Time-series trend analysis of TGM (Total Gaseous Mercury) in air was performed from 10 circumpolar air monitoring stations, comprising of high-Arctic, and sub-Arctic sites. GOM (gaseous oxidised mercury) and PHg (particulate bound mercury) measurements were also available at 2 high-Arctic sites. Seasonal mean TGM for sub-Arctic sites were lowest during fall ranging from 1.1 ng m−3 Hyytiälä to 1.3 ng m−3, Little Fox Lake. Mean TGM concentrations at high-Arctic sites showed the greatest variability, with highest daily means in spring ranging between 4.2 ng m−3 at Amderma and 2.4 ng m−3 at Zeppelin, largely driven by local chemistry. Annual TGM trend analysis was negative for 8 of the 10 sites. High-Arctic seasonal TGM trends saw smallest decline during summer. Fall trends ranged from −0.8% to −2.6% yr−1. Across the sub-Arctic sites spring showed the largest significant decreases, ranging between −7.7% to −0.36% yr−1, while fall generally had no significant trends. High-Arctic speciation of GOM and PHg at Alert and Zeppelin showed that the timing and composition of atmospheric mercury deposition events are shifting. Alert GOM trends are increasing throughout the year, while PHg trends decreased or not significant. Zeppelin saw the opposite, moving towards increasing PHg and decreasing GOM. Atmospheric mercury trends over the last 20 years indicate that Hg concentrations are decreasing across the Arctic, though not uniformly. This is potentially driven by environmental change, such as plant productivity and sea ice dynamics.

Elsevier

2022

2020

Updating historical global inventories of anthropogenic mercury emissions to air. AMAP Technical Report, no. 3, 2010

Wilson, S.; Munthe, J.; Sundseth, K.; Kindbom, K.; Maxzson, P.; Pacyna, J.; Steenhuisen, F.

2010

Updating the OECD 211 Daphnia magna Reproduction Test for Use With Engineered and Anthropogenic Particles

Lynch, Iseult; Reilly, Katie; Guo, Zhiling; Ellis, Laura-Jayne; Serchi, Tommaso; Dusinska, Maria

2022

Uptake and effects of 2, 4, 6 - trinitrotoluene (TNT) in juvenile Atlantic salmon (Salmo salar)

Mariussen, Espen; Stornes, Siv Marie; Bøifot, Kari Oline; Rosseland, Bjørn Olav; Salbu, Brit; Heier, Lene Sørlie

Elsevier

2018

Uptake of organic contaminants from car tire microplastics in Arctic marine species

Halsband, Claudia; Hägg, Fanny; Galtung, Kristin; Herzke, Dorte; Nikiforov, Vladimir; Sperre, Kristine Hopland; Sørensen, Lisbet; Egeness, Mari Jystad; Booth, Andy

Car tire particles represent an important environmental challenge that is difficult to alleviate. The particles stem from abrasion during driving, so-called tire wear particles (TWPs), down-cycled end-oflife tire crumb rubber (CR) granulate that is used widely as low-cost infill on sports fields, or degradation products from discarded tires. The material contains a variety of additives and chemical residues from the manufacturing process, including metals, especially high concentrations of zinc, polycyclic aromatic hydrocarbons (PAHs), and benzothiazoles (Halsband et al., 2020), but also paraphenylenediaminesb (PPDs) and numerous other organic chemicals. In urbanized areas, TWPs arebemitted from vehicles, while CR is dispersed from artificial sports fields and other urban surfaces to the environment. This suggests that particulate and chemical runoff to coastal systems is likely and represents a route of exposure to marine organisms. In the Arctic, even small human settlements can represent local sources of TWPs and CR granulate emissions. Here, we summarize recent experimental studies examining the responses of different marine animals to tire rubber particle or leachate exposure, focusing on toxicity and the uptake kinetics of tire-related organic chemicals into organs and tissues. We present data for different ecological functional groups relevant to the Arctic, including copepods, shrimps, crabs, and fish, representing different body sizes, marine habitats, and feeding modes, and thus varying exposure scenarios. Our findings from GC-HRMS SIM chromatography demonstrate that several tire additives are taken up into tissues. Although the available data indicates many tire-derived organic chemicals do not seem to bioaccumulate, mapping of tire rubber particle and chemical distributions in Arctic coastal systems, dose-response toxicity testing and risk assessments of environmental concentrations are warranted, also with a view to potential trophic transfer within the Arctic marine food chain.

2023

Uptake of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) by river water fish: The case of River Chenab.

Eqani, S.A.-M.-A.-S.; Malik, R.N.; Cincinelli, A.; Zhang, G.; Mohammad, A.; Qadir, A.; Rashid, A.; Bokhari, H.; Jones, K.C.; Katsoyiannis, A.

2013

Urban air pollution 2000-2015. Results from monitoring and modeling in Oslo and Trondheim. NILU OR

Tønnesen, D.

The expected changes in emission profiles for vehicular traffic has been investigated by Ecotraffic on behalf of Statoil. This report gives a trend analysis of monitoring and model results for air quality in Oslo and Trondheim. The period covered is 2000 to 2015, the last third of the period is covered only by modelling. The impact of introduction of bio fuel have been reflected upon, based on the changes in emission profiles given by Ecotraffic. For particulate matter, the introduction of bio fuels will likely contribute to a continuous reduction of ambient air concentrations. For NOX and NO2, introduction of bio fuel will have an adverse effect, and the urban air pollution level of NO2 is no longer decreasing.

2010

Urban air pollution and human health

Cincinelli, Alessandra; Katsoyiannis, Athanasios A.

Elsevier

2019

Urban air pollution and mortality in a cohort of Norwegian men.

Nafstad, P.; Håheim, L. L.; Wisløff, T.; Gram, F.; Oftedal, B.; Holme, I.; Hjermann, I.; Leren, P.

2004

Urban air quality in larger conurbations in the European Union.

de Leeuw, F.A.A.M.; Moussiopoulos, N.; Sahm, P.; Bartonova, A.

2001

Urban Air Quality Perception

Grossberndt, Sonja; Castell, Nuria; Fredriksen, Mirjam; Schneider, Philipp; Bartonova, Alena

2019

Urban background levels of dioxin and PCB in Oslo. NILU OR

Schlabach, M.; Tønnesen, D.

2008

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