Skip to content
  • Submit

  • Category

  • Sort by

  • Per page

Found 10000 publications. Showing page 109 of 400:

Publication  
Year  
Category

Different Sensitivity of Advanced Bronchial and Alveolar Mono- and Coculture Models for Hazard Assessment of Nanomaterials

Elje, Elisabeth; Mariussen, Espen; McFadden, Erin; Dusinska, Maria; Rundén-Pran, Elise

For the next-generation risk assessment (NGRA) of chemicals and nanomaterials, new approach methodologies (NAMs) are needed for hazard assessment in compliance with the 3R’s to reduce, replace and refine animal experiments. This study aimed to establish and characterize an advanced respiratory model consisting of human epithelial bronchial BEAS-2B cells cultivated at the air–liquid interface (ALI), both as monocultures and in cocultures with human endothelial EA.hy926 cells. The performance of the bronchial models was compared to a commonly used alveolar model consisting of A549 in monoculture and in coculture with EA.hy926 cells. The cells were exposed at the ALI to nanosilver (NM-300K) in the VITROCELL® Cloud. After 24 h, cellular viability (alamarBlue assay), inflammatory response (enzyme-linked immunosorbent assay), DNA damage (enzyme-modified comet assay), and chromosomal damage (cytokinesis-block micronucleus assay) were measured. Cytotoxicity and genotoxicity induced by NM-300K were dependent on both the cell types and model, where BEAS-2B in monocultures had the highest sensitivity in terms of cell viability and DNA strand breaks. This study indicates that the four ALI lung models have different sensitivities to NM-300K exposure and brings important knowledge for the further development of advanced 3D respiratory in vitro models for the most reliable human hazard assessment based on NAMs.

2023

Differentiation of coarse-mode anthropogenic, marine and dust particles in the High Arctic islands of Svalbard

Song, Congbo; Dall'Osto, Manuel; Lupi, Angelo; Mazzola, Mauro; Traversi, Rita; Becagli, Silvia; Gilardoni, Stefania; Vratolis, Stergios; Yttri, Karl Espen; Beddows, David C.S.; Schmale, Julia; Brean, James; Kramawijaya, Agung Ghani; Harrison, Roy M.; Shi, Zongbo

Understanding aerosol–cloud–climate interactions in the Arctic is key to predicting the climate in this rapidly changing region. Whilst many studies have focused on submicrometer aerosol (diameter less than 1 µm), relatively little is known about the supermicrometer aerosol (diameter above 1 µm). Here, we present a cluster analysis of multiyear (2015–2019) aerodynamic volume size distributions, with diameter ranging from 0.5 to 20 µm, measured continuously at the Gruvebadet Observatory in the Svalbard archipelago. Together with aerosol chemical composition data from several online and offline measurements, we apportioned the occurrence of the coarse-mode aerosols during the study period (mainly from March to October) to anthropogenic (two sources, 27 %) and natural (three sources, 73 %) origins. Specifically, two clusters are related to Arctic haze with high levels of black carbon, sulfate and accumulation mode (0.1–1 µm) aerosol. The first cluster (9 %) is attributed to ammonium sulfate-rich Arctic haze particles, whereas the second one (18 %) is attributed to larger-mode aerosol mixed with sea salt. The three natural aerosol clusters were open-ocean sea spray aerosol (34 %), mineral dust (7 %) and an unidentified source of sea spray-related aerosol (32 %). The results suggest that sea-spray-related aerosol in polar regions may be more complex than previously thought due to short- and long-distance origins and mixtures with Arctic haze, biogenic and likely blowing snow aerosols. Studying supermicrometer natural aerosol in the Arctic is imperative for understanding the impacts of changing natural processes on Arctic aerosol.

2021

Diffuse utslipp ved lossing ved Boliden. Metodeutvikling og resultat.

Grythe, Henrik; Uggerud, Hilde Thelle; Andresen, Erik; Bäcklund, Are; Weydahl, Torleif

NILU

2021

DIGG-MIN-SKOLE: prosjektgjennomgang for Standard Norge

Bartonova, Alena; Høiskar, Britt Ann Kåstad; Fredriksen, Mirjam; Fredriksen, Tore

2025

DIGG-MIN-SKOLE: verktøy for samarbeid om inneklima i skolen

Fredriksen, Tore; Bartonova, Alena; Høiskar, Britt Ann Kåstad; Fredriksen, Mirjam

2025

Digital technologies for environmental footprints and product passports

Bouman, Evert Alwin; Abbasi, Golnoush; Ebrahimi, Babak

2022

Dimethyl Sulfide-Induced Increase in Cloud Condensation Nuclei in the Arctic Atmosphere

Park, Ki-Tae; Yoon, Young Jun; Lee, Kitack; Tunved, Peter; Krejci, Radovan; Ström, Johan; Jang, Eunho; Kang, Hyo Jin; Jang, Seyhun; Park, Jiyeon; Lee, Bang Young; Traversi, Rita; Becagli, Silvia; Hermansen, Ove

Oceanic dimethyl sulfide (DMS) emissions have been recognized as a biological regulator of climate by contributing to cloud formation. Despite decades of research, the climatic role of DMS remains ambiguous largely because of limited observational evidence for DMS-induced cloud condensation nuclei (CCN) enhancement. Here, we report concurrent measurement of DMS, physiochemical properties of aerosol particles, and CCN in the Arctic atmosphere during the phytoplankton bloom period of 2010. We encountered multiple episodes of new particle formation (NPF) and particle growth when DMS mixing ratios were both low and high. The growth of particles to sizes at which they can act as CCN accelerated in response to an increase in atmospheric DMS. Explicitly, the sequential increase in all relevant parameters (including the source rate of condensable vapor, the growth rate of particles, Aitken mode particles, hygroscopicity, and CCN) was pronounced at the DMS-derived NPF and particle growth events. This field study unequivocally demonstrates the previously unconfirmed roles of DMS in the growth of particles into climate-relevant size and eventual CCN activation.

2021

Dioxin-like chemicals in soil and sediment from residential and industrial areas in Central South Africa.

Nieuwoudt, C.; Quinn, L.P.; Pieters, R.; Jordaan, I.; Visser, M.; Kylin, H.; Borgen, A.R.; Giesy, J.P.; Bouwman, H.

2009

Dioxins in freshwater fish and soil from Lenvik municipality, Troms county. NILU OR

Heimstad, E.S.; Dahl-Hansen, G.A.P.; Schlabach, M.; Enge, E.K.

2007

Direct and indirect electron precipitation effect on nitric oxide during the April 2010 electron precipitation events, Part 1: Observations, Part 2: WACCM.

Tyssøy, H. N.; Smith-Johnsen, C.; Orsolini, Y.; Marsh, D. R.; Hendrickx, K.; Sandanger, M. I. J.; Ødegaard, L.-K. G.; Kishore Kumar, G.; Stordal, F.; Megner, L.

2017

Direct and indirect electron precipitation effect on nitric oxide in the polar middle atmosphere, using a full-range energy spectrum.

Smith-Johnsen, C.; Nesse Tyssøy, H.; Hendrickx, K.; Orsolini, Y.; Kishore Kumar, G.; Ødegaard, L.-K. G.; Sandanger, M. I.; Stordal, F.; Megner, L.

2017

Direct and indirect electron precipitation effect on nitric oxide, using a full range energy spectrum.

Smith-Johnsen, C.; Tyssøy, H. N.; Hendrickx, K.; Orsolini, Y.; Kishore Kumar, G.; Ødegaaard, L.-K. G.; Stordal, F.; Megner, L.

2017

Direct transport of midlatitude stratospheric ozone into the lower troposphere and marine boundary layer of the tropical Pacific Ocean.

Cooper, O.; Stohl, A.; Hübler, G.; Hsie, E.Y.; Parrish, D.D.; Tuck, A.F.; Kiladis, G.N.; Oltmans, S.J.; Johnson, B.J.; Shapiro, M.; Moody, J.L.; Lefohn, A.

2005

Direct validation of satellite-derived trends in tropospheric NO2 with ground-based MAX-DOAS instruments. NILU F

Schneider, P.; Stebel, K.; Pinardi, G.; van Roozendael, M.; Hendrick, F.; Kanaya, Y.

2014

Discharges of oil and environmentally dangerous chemicals to Norwegian marine areas, phase II. NIVA rapport, 5624-2008

Molvær, J.; Barret, K.; Barkved, L.; Iosjpe, M.; Jantsch, T.G.; Kaste, Ø.; Saloranta,T.; Selvik, J.R.; Skaare, B.B.; Wehde, H.

2008

Discounting the effect of meteorology on trends in surface ozone: Development of statistical tools

Solberg, Sverre; Walker, Sam-Erik; Schneider, Philipp; Guerreiro, Cristina; Colette, Augustin

This report presents the results using a statistical method to single out the influence of interannual meteorological variability on surface ozone. The reason for using such a tool is two-fold: Firstly, to explain the ozone levels in one specific year in terms of weather anomalies and secondly, to estimate the part of long-term ozone trends that is due to the meteorology alone. The method is a so-called GAM (generalized additive model), which could be regarded an advanced multiple regression method relating daily ozone levels to certain meteorological variables. The performance of the method was evaluated by comparing observed ozone data with those predicted by the GAM. This revealed a good to very good agreement in central Europe and Germany in particular. For southern Europe the performance was poorer. The method indicated that meteorology contributed to the downward trend in ozone seen at most sites for both 1990-2000 and 2000-2010.

ETC/ACM

2018

Discounting the impact of meteorology to the ozone concentration trends. ETC/ACM Technical Paper, 2015/9

Solberg, S.; Colette, A.; Bessagnet, B.; Réal, E.; Couvidat, F.; Guerreiro, C.

2015

Discrepancy between simulated and observed ethane and propane levels explained by underestimated fossil emissions

Dalsøren, Stig Bjørløw; Myhre, Gunnar; Hodnebrog, Øivind; Myhre, Cathrine Lund; Stohl, Andreas; Pisso, Ignacio; Schwietzke, Stefan; Höglund-Isaksson, Lena; Helmig, Detlev; Reimann, Stefan; Sauvage, Stéphane; Schmidbauer, Norbert; Read, Katie A.; Carpenter, Lucy J.; Lewis, Alastair C.; Punjabi, Shalini; Wallasch, Markus

2018

Discussion on the representativeness of current methodologies to assess indoor air quality

Vogt, Matthias; Hak, Claudia; Lopez-Aparicio, Susana; Dauge, Franck Rene; Holøs, Sverre Bjørn; Yang, Aileen; Mysen, Mads

2018

Publication
Year
Category