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Evaluation of observed and modelled aerosol lifetimes - using radioactive tracers of opportunity and an ensemble of 19 global models. NILU PP

Kristiansen, N.I.; Stohl, A.; Christoudias, T.; Kunkel, D.; Croft, B.; Pierce, J.; Martin, R.; Bergman, T.; Kokkola, H.; Lee, Y.H.; Shindell, D.; Pitari, G.; Di Genova, G.; Zhang, H.; Zhao, S.; Søvde, O.A., Wang, H.; Zhang, K.; Liu, X.; Evangeliou, N.; Balanski, Y.; Tsigaridis, K.; Bauer, S.; Klein, H.; Leadbetter, S.; Olivié, D.J.L.; Schulz, M.

2014

Evaluation of novel cleaning systems on mock-ups of unvarnished oil paint and chalk-glue ground within the Munch Aula Paintings Project

Stoveland, Lena Porsmo; Frøysaker, Tine; Stols-Witlox, Maartje; Grøntoft, Terje; Steindal, Calin Constantin; Madden, Odile; Ormsby, Bronwyn

BioMed Central (BMC)

2021

Evaluation of new data sources for improving the estimation of background concentrations in Norway. NILU OR

Schneider, P.; Obracaj, A.

A previous report (OR 68/2011) described a geostatistical methodology developed for creating a consistent dataset of background concentrations of NO2, O3, PM10, and PM2.5 in Norway, that are representative of a typical year. The resulting dataset has a resolution of 0.1 degrees by 0.1 degrees and is available at hourly temporal resolution. Based on this existing methodology, this study reports on the evaluation of new data sources as a means of improving such estimates of background concentrations. The potential of satellite-derived NO2 data is evaluated for guiding the geostatistics-based spatial interpolation procedure of NO2 station data in Norway. Furthermore, the output from a high-resolution atmospheric model was tested with respect to its capability of improving the spatial and temporal characterization of background concentrations. Finally, an online web mapping system was developed to make the project results easily accessible and to provide basic data analysis and visualization routines for the public.

2013

Evaluation of multidecadal high-resolution atmospheric chemistry-transport modelling for exposure assessments in the continental Nordic countries

Frohn, Lise Marie; Geels, Camilla; Andersen, Christopher; Andersson, Camilla; Bennet, Cecilia; Christensen, Jesper H.; Im, Ulas; Karvosenoja, Niko; Kukkonen, Jaakko; Lopez-Aparicio, Susana; Nielsen, Ole-Kenneth; Palamarchuk, Yuliia; Paunu, Ville-Veikko; Plejdrup, Marlene S.; Segersson, David; Sofiev, Mikhail; Brandt, Jørgen

Elsevier

2022

Evaluation of monitoring PM with low-cost monitor and conventional devices.

Jovaševic-Stojanovic, M.; Bartonova, A.; Topaloviv, D.; Davidovic, M.; Lazovic, I.; Ristovski, Z.

2016

Evaluation of modelled versus observed non-methane volatile organic compounds at European Monitoring and Evaluation Programme sites in Europe

Ge, Yao; Solberg, Sverre; Heal, Mathew R; Reimann, Stefan; van Caspel, Willem; Hellack, Bryan; Salameh, Therese; Simpson, David

Atmospheric volatile organic compounds (VOCs) constitute a wide range of species, acting as precursors to ozone and aerosol formation. Atmospheric chemistry and transport models (CTMs) are crucial to understanding the emissions, distribution, and impacts of VOCs. Given the uncertainties in VOC emissions, lack of evaluation studies, and recent changes in emissions, this work adapts the European Monitoring and Evaluation Programme Meteorological Synthesizing Centre – West (EMEP MSC-W) CTM to evaluate emission inventories in Europe. Here we undertake the first intensive model–measurement comparison of VOCs in 2 decades. The modelled surface concentrations are evaluated both spatially and temporally, using measurements from the regular EMEP monitoring network in 2018 and 2019, as well as a 2022 campaign. To achieve this, we utilised the UK National Atmospheric Emissions Inventory to derive explicit emission profiles for individual species and employed a tracer method to produce pure concentrations that are directly comparable to observations.

The degree to which the modelled and measured VOCs agree varies depending on the specific species. The model successfully captures the overall spatial and temporal variations of major alkanes (e.g. ethane, n-butane) and unsaturated species (e.g. ethene, benzene) but less so for propane, i-butane, and ethyne. This discrepancy underscores potential issues in the boundary conditions for the latter species and in their primary emissions from, in particular, the solvent and road transport sectors. Specifically, potential missing propane emissions and issues with its boundary conditions are highlighted by large model underestimations and smaller propane-to-ethane ratios compared to the measurement. Meanwhile, both the model and measurements show strong linear correlations among butane isomers and among pentane isomers, indicating common sources for these pairs of isomers. However, modelled ratios of i-butane to n-butane and i-pentane to n-pentane are approximately one-third of the measured ratios, which is largely driven by significant emissions of n-butane and n-pentane from the solvent sector. This suggests issues with the speciation profile of the solvent sector, underrepresented contributions from transport and fuel evaporation sectors in current inventories, or both. Furthermore, the modelled ethene-to-ethyne and benzene-to-ethyne ratios differ significantly from measured ratios. The different model performance strongly points to shortcomings in the spatial and temporal patterns and magnitudes of ethyne emissions, especially during winter. For OVOCs, the modelled and measured concentrations of methanal and methylglyoxal show a good agreement, despite a moderate underestimation by the model in summer. This discrepancy could be attributed to an underestimation of contributions from biogenic sources or possibly a model overestimation of their photolytic loss in summer. However, the insufficiency of suitable measurements limits the evaluation of other OVOCs. Finally, model simulations employing the CAMS inventory show slightly better agreements with measurements than those using the Centre on Emission Inventories and Projections (CEIP) inventory. This enhancement is likely due to the CAMS inventory's detailed segmentation of the road transport sector, including its associated sub-sector-specific emission profiles. Given this improvement, alongside the previously mentioned concerns about the model's biased estimations of various VOC ratios, future efforts should focus on a more detailed breakdown of dominant emission sectors (e.g. solvents) and the refinement of their speciation profiles to improve model accuracy.

2024

Evaluation of modelled versus observed NMVOC compounds at EMEP sites in Europe

Ge, Yao; Simpson, David; Solberg, Sverre; Heal, Mathew; Reimann, Stefan; van Caspel, Willem; Hellack, Bryan; Salameh, Therese

2024

Evaluation of meso- and microplastic ingestion by the northern fulmar through a non-lethal sampling method

Collard, France; Strøm, Hallvard; Fayet, Marie-Océane; Gudmundsson, Fannar Theyr; Herzke, Dorte; Hotvedt, Ådne; Løchen, Arja; Malherbe, Cédric; Eppe, Gauthier; Gabrielsen, Geir W.

An increasing number of organisms from the polar regions are reported contaminated by plastic. Rarely a non-killing sampling method is used. In this study we wanted to assess plastic levels using stomach flushing and evaluate the method suitability for further research and monitoring. The stomach of 22 fulmars from Bjørnøya, Svalbard, were flushed with water in the field. On return to the laboratory, the regurgitated content was digested using potassium hydroxide. The extracted plastics were visually characterised and analysed with spectroscopy. Only three birds had plastics in their stomach, totaling 36 particles, most of them microplastics (< 5 mm). The plastic burdens are much lower than previously reported in Svalbard. The stomach flushing is assumed not to allow the collection of the gizzard content. This is a major limitation as most of the plastics accumulate in the fulmar's gizzard. However, the method is still useful for studies investigating plastic ingestion dynamics, allowing to sample the same individuals over time.

Elsevier

2023

Evaluation of isoprene emissions from the coupled model SURFEX–MEGANv2.1

Oumami, Safae; Arteta, Joaquim; Guidard, Vincent; Tulet, Pierre; Hamer, Paul David

Isoprene, a key biogenic volatile organic compound, plays a pivotal role in atmospheric chemistry. Due to its high reactivity, this compound contributes significantly to the production of tropospheric ozone in polluted areas and to the formation of secondary organic aerosols.

The assessment of biogenic emissions is of great importance for regional and global air quality evaluation. In this study, we implemented the biogenic emission model MEGANv2.1 (Model of Emissions of Gases and Aerosols from Nature, version 2.1) in the surface model SURFEXv8.1 (SURface EXternalisée in French, version 8.1). This coupling aims to improve the estimation of biogenic emissions using the detailed vegetation-type-dependent treatment included in the SURFEX vegetation ISBA (Interaction between Soil Biosphere and Atmosphere) scheme. This scheme provides vegetation-dependent parameters such as leaf area index and soil moisture to MEGAN. This approach enables a more accurate estimation of biogenic fluxes compared to the stand-alone MEGAN model, which relies on average input values for all vegetation types.

The present study focuses on the assessment of the SURFEX–MEGAN model isoprene emissions. An evaluation of the coupled SURFEX–MEGAN model results was carried out by conducting a global isoprene emission simulation in 2019 and by comparing the simulation results with other MEGAN-based isoprene inventories. The coupled model estimates a total global isoprene emission of 443 Tg in 2019. The estimated isoprene is within the range of results obtained with other MEGAN-based isoprene inventories, ranging from 311 to 637 Tg. The spatial distribution of SURFEX–MEGAN isoprene is consistent with other studies, with some differences located in low-isoprene-emission regions.

Several sensitivity tests were conducted to quantify the impact of different model inputs and configurations on isoprene emissions. Using different meteorological forcings resulted in a ±5 % change in isoprene emissions using MERRA (Modern-Era Retrospective analysis for Research and Applications) and IFS (Integrated Forecasting System) compared with ERA5. The impact of using different emission factor data was also investigated. The use of PFT (plant functional type) spatial coverage and PFT-dependent emission potential data resulted in a 12 % reduction compared to using the isoprene emission potential gridded map. A significant reduction of around 38 % in global isoprene emissions was observed in the third sensitivity analysis, which applied a parameterization of soil moisture deficit, particularly in certain regions of Australia, Africa, and South America.

The significance of coupling the SURFEX and MEGAN models lies particularly in the ability of the coupled model to be forced with meteorological data from any period. This means, for instance, that this system can be used to predict biogenic emissions in the future. This aspect of our work is significant given the changes that biogenic organic compounds are expected to undergo as a result of changes in their climatic factors.

2024

Evaluation of inventories of heavy metals and persistent organic pollutants within the convention on LRTAP. EMEP/MSC-W Technical report, 1/2006

Pacyna, J.M.; van der Gon, H.D.; Reis, S.; Travnikov, O.; Vestreng, V.

2006

Evaluation of interannual variability of Arctic and Antarctic ozone loss since 198

Goutail, Florence; Pazmino, Andrea; Pommereau, Jean-Pierre; Lefevre, Franck; Godin-Beekmann, Sophie; Hauchecorne, Alain; Lecouffe, Audrey; Clerbaux, Cathy; Boynard, Anne; Hadji-Lazaro, Juliette; Chipperfield, Martyn P.; Feng, Wuhu; Van Roozendael, Michel; Jepsen, Nis; Hansen, Georg Heinrich; Kivi, Rigel; Bognar, Kristof; Strong, Kimberly; Walker, Kaley A.; Colwell, Steve

2021

Evaluation of high-resolution air pollution modelling for the continental Nordic countries

Frohn, Lise Marie; Brandt, Jørgen; Andersson, Camilla; Anderssen, Christopher; Bennet, Cecilia; Christensen, Jesper H.; Im, Ulas; Karvosenoja, Niko; Kukkonen, Jaakko; Lopez-Aparicio, Susana; Nielsen, Ole-Kenneth; Palamarchuk, Yuliia; Paunu, Ville-Veikko; Pleljdrup, Marlene Smith; Segersson, David; Sofiev, Mikhail; Geels, Camilla

2021

Evaluation of Global Ozone Monitoring Experiment (GOME) ozone profiles from nine different algorithms.

Meijer, Y.J.; Swart, D.P.J.; Baier, F.; Bhartia, P.K.; Bodeker, G.E.; Casadio, S.; Chance, K.; Del Frate, F.; Erbertseder, T.; Felder, M.D.; Flynn, L.E.; Godin-Beekmann, S.; Hansen, G.; Hasekamp, G.; Kaifer, A.; Kelder, H.M.; Kerridge, B.J.; Lambert, J.-C.; Landgraf, J.; Latter, B.; Liu, X.; McDermid, I.S.; Pachepsky, Y.; Rozanov, V.; Siddans, R.; Tellmann, S.; van der A, R.J.; van Oss, R.F.; Weber, M.; Zehner, C.

2006

Evaluation of global models abilities to assess the regional and global sulfate aerosol trends, 1990-2015

Aas, Wenche; Mortier, Augustin; Cherian, Ribu; Oliviè, Dirk Jan Leo; Faluvegi, Greg; Hand, Jenny; Lehmann, Christopher M. B.; Myhre, Cathrine Lund; Myhre, Gunnar; Sato, Keiichi; Schulz, Michael; Shindell, Drew; Takemura, Toshihiko; Tsyro, Svetlana; Quaas, Johannes

2018

Evaluation of existing Air Quality Network. Abu Dhabi Air Quality Management Study. NILU OR

Bøhler, T.; Guerreiro, C.; Marsteen, L.; Sivertsen, B.

2004

Evaluation of Copernicus MACC-II ensemble products in the ETC/ACM spatial air quality mapping. ETC/ACM Technical Paper, 2013/9

Horalek, J.; Tarrasón, L.; de Smet, P.; Malherbe, L.; Schneider, P.; Ung, A.; Corbet, L.; Denby, B.

2014

Evaluation of climate model aerosol trends with ground-based observations over the last 2 decades – an AeroCom and CMIP6 analysis

Mortier, Augustin; Gliss, Jonas; Schulz, Michael; Aas, Wenche; Andrews, Elisabeth; Bian, Huisheng; Chin, Mian; Ginoux, Paul; Hand, Jenny; Holben, Brent; Zhang, Hua; Kipling, Zak; Kirkevåg, Alf; Laj, Paolo; Lurton, Thibault; Myhre, Gunnar; Neubauer, David; Oliviè, Dirk Jan Leo; Salzen, Knut von; Skeie, Ragnhild Bieltvedt; Takemura, Toshihiko; Tilmes, Simone

2020

Evaluation of AOD uncertainties in three 17-year ATSR-2/AATSR retrievals.

Stebel, K.; Povey, A.; Heckel, A.; Kinne, S.; Kolmonen, P.; de Leeuw, G.; North, P.; Sogacheva, L.; Thomas, G.; Popp, T.

2016

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