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Annual report 2024. National reference laboratory for air quality monitoring
No full textDenne rapporten oppsummerer oppgavene til Nasjonalt referanselaboratorium for luftkvalitetsmålinger (NRL), delkontrakt 1b, for året 2024.This annual report summarizes the work of National reference laboratory for air quality monitoring (NRL), sub contract 1b, for the year 2024.publishedVersio
Metals, PCB, PAH and dioxins in the Russian-Norwegian border areas. Moss survey 2008, 2015, 2020
No full textI 2008 samlet Svanhovd Miljøsenter inn mose ved lokaliteter i grenseområdene mot Russland som NILU analyserte for 11 metaller, PCB, PAH og dioksiner. Formålet var å undersøke om det var andre kilder til forurensning i grenseområdene enn gruvedrift og smelteverksindustri. Prøvetaking og analyse ble gjentatt av NILU i 2015 og 2020, men kun for 60 (2015) og 56 (2020) metaller. For spormetallene Ni, Cu, Co og As er det et klart mønster med forhøyede konsentrasjoner nedstrøms Nikel og Zapolyarnyj. Organiske miljøgifter viser lave konsentrasjoner.publishedVersio
A European aerosol phenomenology – 9: Light absorption properties of carbonaceous aerosol particles across surface Europe
Full text linkCarbonaceous aerosols (CA), composed of black carbon (BC) and organic matter (OM), significantly impact the climate. Light absorption properties of CA, particularly of BC and brown carbon (BrC), are crucial due to their contribution to global and regional warming. We present the absorption properties of BC (bAbs,BC) and BrC (bAbs,BrC) inferred using Aethalometer data from 44 European sites covering different environments (traffic (TR), urban (UB), suburban (SUB), regional background (RB) and mountain (M)). Absorption coefficients showed a clear relationship with station setting decreasing as follows: TR > UB > SUB > RB > M, with exceptions. The contribution of bAbs,BrC to total absorption (bAbs), i.e. %AbsBrC, was lower at traffic sites (11–20 %), exceeding 30 % at some SUB and RB sites. Low AAE values were observed at TR sites, due to the dominance of internal combustion emissions, and at some remote RB/M sites, likely due to the lack of proximity to BrC sources, insufficient secondary processes generating BrC or the effect of photobleaching during transport. Higher bAbs and AAE were observed in Central/Eastern Europe compared to Western/Northern Europe, due to higher coal and biomass burning emissions in the east. Seasonal analysis showed increased bAbs, bAbs,BC, bAbs,BrC in winter, with stronger %AbsBrC, leading to higher AAE. Diel cycles of bAbs,BC peaked during morning and evening rush hours, whereas bAbs,BrC, %AbsBrC, AAE, and AAEBrC peaked at night when emissions from household activities accumulated. Decade-long trends analyses demonstrated a decrease in bAbs, due to reduction of BC emissions, while bAbs,BrC and AAE increased, suggesting a shift in CA composition, with a relative increase in BrC over BC. This study provides a unique dataset to assess the BrC effects on climate and confirms that BrC can contribute significantly to UV–VIS radiation presenting highly variable absorption properties in Europe.publishedVersio
Citizen-operated low-cost sensors for estimating outdoor particulate matter infiltration
No full textFine particulates observed indoors exhibit high variability, influenced by both indoor emission sources and the infiltration of outdoor particles through open spaces and the incomplete building insulation. This study examines the relationship between indoor and outdoor PM2.5 levels in Legionowo, Poland, using data from low-cost air quality sensors operated by citizens. The indoor PM2.5 was lower than outdoor levels (median PM2.5: 1.9–17.3 μg m–3 indoors and 6.7–27.9 μg m–3 outdoors), with occasional peaks attributed to potential indoor emission sources. Statistical analysis identified emission events—particularly during cooking and household-heating periods—occurring more frequently from October to April. During this period, nearly 17% of indoor PM2.5 measurements were attributed to indoor emission sources after 18:00 LT, representing a 7% increase compared to the May–September period. In the absence of indoor sources, outdoor particles accounted for 29% to 75% of indoor concentrations, highlighting the significance of infiltration. This research emphasizes how citizen-generated data using low-cost sensors, after post-processing, can provide decision-ready information as for example outdoor particles’ infiltration factors for each building. The knowledge of the infiltration factor enables the determination of the contribution of indoor and outdoor sources to each resident’s exposure to airborne PM. This information can help decision-makers in devising interventions such as prioritizing indoor ventilation, reducing indoor activities resulting in increased exposure, and addressing outdoor pollution sources.publishedVersio
Uptake of chemicals from tire wear particles into aquatic organisms - search for biomarkers of exposure in blue mussels
Full text linkLittle is known about the exposure of aquatic biota to tire and road wear particles (TRWP) washed away from roads. Mussels were exposed for 7 days to model TRWP (m-TRWP), produced by milling tire tread particles with pure sand, and analyzed for 21 tire-related compounds by liquid chromatography-high resolution-mass spectrometry (LC-HRMS). Upon exposure to 0.5 g/L of m-TRWP, 15 compounds were determined from 944 μg/kg wet weight (diphenylguanidine, DPG) over 18 μg/kg for an oxidation product of N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6-PPDQ) to 0.6 μg/kg (4-hydroxydiphenyl amine). Transfer into mussels was highest for PTPD, DTPD and 6-PPDQ and orders of magnitude lower for 6-PPD. During 7 days depuration the concentration of all determined chemicals decreased to remaining concentrations between ~50 % (PTPD, DTPD) and 6 % (6-PPD). Suspect and non-target screening found 37 additional transformation products (TPs) of tire additives, many of which did not decrease in concentration during depuration, among them ten likely TPs of DPG, two of 6-PPD and PTPD and two of 1,2-dihydro-2,2,4-trimethylquinoline. A wide variety of chemicals is taken up by mussels upon exposure to m-TRWP and a wide range of TPs is formed, enabling the differentiation of biomarkers of exposure to TRWP and biomarkers of exposure to tire-associated chemicals.publishedVersio
Future CH4 as modelled by a fully coupled Earth system model: prescribed GHG concentrations vs. interactive CH4 sources and sinks
Full text linkWe have used the NASA Goddard Institute for Space Studies (GISS) Earth system model GISS-E2.1 to study the future budgets and trends of global and regional CH4 under different emission scenarios, using both the prescribed GHG concentrations as well as the interactive CH4 sources and sinks setup of the model, to quantify the model performance and its sensitivity to CH4 sources and sinks. We have used the Current Legislation (CLE) and the maximum feasible reduction (MFR) emission scenarios from the ECLIPSE V6b emission database to simulate the future evolution of CH4 sources, sinks, and levels from 2015 to 2050. Results show that the prescribed GHG version underestimates the observed surface CH4 concentrations during the period between 1995 and 2023 by 1%, with the largest underestimations over the continental emission regions, while the interactive simulation underestimates the observations by 2%, with the biases largest over oceans and smaller over the continents. For the future, the MFR scenario simulates lower global surface CH4 concentrations and burdens compared to the CLE scenario, however in both cases, global surface CH4 and burden continue to increase through 2050 compared to present day. In addition, the interactive simulation calculates slightly larger O3 and OH mixing ratios, in particular over the northern hemisphere, leading to slightly decreased CH4 lifetime in the present day. The CH4 forcing is projected to increase in both scenarios, in particular in the CLE scenario, from 0.53 W m−2 in the present day to 0.73 W m−2 in 2050. In addition, the interactive simulations estimate slightly higher tropospheric O3 forcing compared to prescribed simulations, due to slightly higher O3 mixing ratios simulated by the interactive models. While in the CLE, tropospheric O3 forcing continues to increase, the MFR scenario leads to a decrease in tropospheric O3 forcing, leading to a climate benefit. Our results highlight that in the interactive models, the response of concentrations are not necessarily linear with the changes in emissions as the chemistry is non-linear, and dependent on the oxidative capacity of the atmosphere. Therefore, it is important to have the CH4 sources and chemical sinks to be represented comprehensively in climate models.publishedVersio
Methane emissions from Australia estimated by inverse analysis using in-situ and Satellite (GOSAT) atmospheric observations
Full text linkAustralia has significant sources of atmospheric methane (CH₄), driven by extensive coal and natural gas production, livestock, and large-scale fires. Accurate quantification and characterization of CH₄ emissions are critical for effective climate mitigation strategies in Australia. In this study, we employed an inverse analysis of atmospheric CH₄ observations from the GOSAT satellite and surface measurements from 2016 to 2021 to assess CH₄ emissions in Australia. The inversion process integrates anthropogenic and natural emissions as prior estimates, optimizing them with the NIES-TM-FLEXPART-variational model (NTFVAR) at a resolution of up to 0.1° × 0.1°. We validated the performance of our inverse model using data obtained from the United Nations Environment Program Methane Science (UNEP), Airborne Research Australia 2018 aircraft-based atmospheric CH₄ measurement campaigns. Compared to prior emission estimates, optimized emissions dramatically enhanced the accuracy of modeled concentrations, aligning them much better with observations. Our results indicate that the estimated inland CH4 emissions in Australia amount to 6.84 ± 0.51 Tg CH4 yr−1 and anthropogenic emissions amount to 4.20 ± 0.08 Tg CH4 yr−1, both slightly lower than the values reported in existing inventories. Moreover, our results unveil noteworthy spatiotemporal characteristics, such as upward corrections during the warm season, particularly in Southeastern Australia. During the three most severe months of the 2019–2020 bushfire season, emissions from biomass burning surged by 0.68 Tg, constituting over 71% of the total emission increase. These results highlight the importance of continuous observation and analysis of sectoral emissions, particularly near major sources, to guide targeted emission reduction strategies. The spatiotemporal characteristics identified in this study underscore the need for adaptive and region-specific approaches to CH₄ emission management in Australia.Methane emissions from Australia estimated by inverse analysis using in-situ and Satellite (GOSAT) atmospheric observationspublishedVersio
Anthropogenic compounds in the northernmost Atlantic puffin population
Full text linkContamination by organic pollutants, even in remote regions, poses a growing threat to wildlife, including seabirds. However, for many seabirds breeding at high latitudes, both the extent and nature of contaminant exposure remain largely unknown. This study aimed to identify the persistent organic pollutants (POPs) present in the Svalbard Atlantic puffin Fratercula arctica at the northern limit of its range. We also compare contaminant concentrations with those found in other species breeding on Svalbard and in puffin colonies further south. The Svalbard puffins were found to be contaminated by organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and per- and polyfluoroalkyl substances (PFAS). No significant sex difference was found. OCPs, PCBs and/or PFASs concentrations in Svalbard puffins were comparable to those of Brünnich's guillemots Uria lomvia, black guillemots Cepphus grylle, and/or little auks Alle alle, but lower than in glaucous gulls Larus hyperboreus. PFAS concentrations were also lower than in black-legged kittiwakes Rissa tridactyla. OCP and PCB concentrations were lower on Svalbard than in puffin colonies further south. This study is the first to document PFAS concentrations in puffins, therefore it remains unknown whether PFAS levels were also lower on Svalbard than further south. These comparisons should be interpreted with caution, as data for different species or colonies were collected in different years, and contaminant levels vary over time. The current contaminant concentrations indicate that Svalbard puffins are still at low risk for biological effects, but continued monitoring is needed to assess potential future changes.publishedVersio
Addressing the advantages and limitations of using Aethalometer data to determine the optimal absorption Ångström exponents (AAEs) values for eBC source apportionment
Full text linkThe apportionment of equivalent black carbon (eBC) to combustion sources from liquid fuels (mainly fossil; eBCLF) and solid fuels (mainly non-fossil; eBCSF) is commonly performed using data from Aethalometer instruments (AE approach). This study evaluates the feasibility of using AE data to determine the absorption Ångström exponents (AAEs) for liquid fuels (AAELF) and solid fuels (AAESF), which are fundamental parameters in the AE approach. AAEs were derived from Aethalometer data as the fit in a logarithmic space of the six absorption coefficients (470–950 nm) versus the corresponding wavelengths. The findings indicate that AAELF can be robustly determined as the 1st percentile (PC1) of AAE values from fits with R2 > 0.99. This R2-filtering was necessary to remove extremely low and noisy-driven AAE values commonly observed under clean atmospheric conditions (i.e., low absorption coefficients). Conversely, AAESF can be obtained from the 99th percentile (PC99) of unfiltered AAE values. To optimize the signal from solid fuel sources, winter data should be used to calculate PC99, whereas summer data should be employed for calculating PC1 to maximize the signal from liquid fuel sources. The derived PC1 (AAELF) and PC99 (AAESF) values ranged from 0.79 to 1.08, and 1.45 to 1.84, respectively. The AAESF values were further compared with those constrained using the signal at mass-to-charge 60 (m/z 60), a tracer for fresh biomass combustion, measured using aerosol chemical speciation monitor (ACSM) and aerosol mass spectrometry (AMS) instruments deployed at 16 sites. Overall, the AAESF values obtained from the two methods showed strong agreement, with a coefficient of determination (R2) of 0.78. However, uncertainties in both approaches may vary due to site-specific sources, and in certain environments, such as traffic-dominated sites, neither approach may be fully applicable.publishedVersio
Measurement Report: Changes in ammonia emissions since the 18th century in south-eastern Europe inferred from an Elbrus (Caucasus, Russia) ice-core record
Full text linkAtmospheric ammonia (NH3) is a key transboundary air pollutant that contributes to the impacts of nitrogen and acidity on terrestrial ecosystems. Ammonia also contributes to the atmospheric aerosol that affects air quality. Emission inventories indicate that NH3 was predominantly emitted by agriculture over the 19th and 20th centuries but, up to now, these estimates have not been compared to long-term observations. To document past atmospheric NH3 pollution in south-eastern Europe, ammonium (NH) was analysed along an ice core extracted from Mount Elbrus in the Caucasus, Russia. The NH ice-core record indicates a 3.5-fold increase in concentrations between 1750 and 1990 CE. Remaining moderate prior to 1950 CE, the increase then accelerated to reach a maximum in 1989 CE. Comparison between ice-core trends and estimated past emissions using state-of-the-art atmospheric transport modelling of submicron-scale aerosols (FLEXPART (FLEXible PARTicle dispersion) model) indicates good agreement with the course of estimated NH3 emissions from south-eastern Europe since ∼ 1750 CE, with the main contributions from south European Russia, Türkiye, Georgia, and Ukraine. Examination of ice deposited prior to 1850 CE, when agricultural activities remained limited, suggests an NH ice concentration related to natural soil emissions representing ∼ 20 % of the 1980–2009 CE NH level, a level mainly related to current agricultural emissions that almost completely outweigh biogenic emissions from natural soil. These findings on historical NH3 emission trends represent a significant contribution to the understanding of ammonia emissions in Europe over the last 250 years.publishedVersio