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The Modeled Seasonal Cycles of Surface N2O Fluxes and Atmospheric N2O

Sun, Qing; Joos, Fortunat; Lienert, Sebastian; Berthet, Sarah; Carroll, Dustin; Gong, Cheng; Ito, Akihiko; Jain, Atul K.; Kou-Giesbrecht, Sian; Landolfi, Angela; Manizza, Manfredi; Pan, Naiqing; Prather, Michael; Regnier, Pierre; Resplandy, Laure; Séférian, Roland; Shi, Hao; Suntharalingam, Parvadha; Thompson, Rona Louise; Tian, Hanqin; Vuichard, Nicolas; Zaehle, Sönke; Zhu, Qing

Nitrous oxide (N2O) is a greenhouse gas and stratospheric ozone-depleting substance with large and growing anthropogenic emissions. Previous studies identified the influx of N2O-depleted air from the stratosphere to partly cause the seasonality in tropospheric N2O (aN2O), but other contributions remain unclear. Here, we combine surface fluxes from eight land and four ocean models from phase 2 of the Nitrogen/N2O Model Intercomparison Project with tropospheric transport modeling to simulate aN2O at eight remote air sampling sites for modern and pre-industrial periods. Models show general agreement on the seasonal phasing of zonal-average N2O fluxes for most sites, but seasonal peak-to-peak amplitudes differ several-fold across models. The modeled seasonal amplitude of surface aN2O ranges from 0.25 to 0.80 ppb (interquartile ranges 21%–52% of median) for land, 0.14–0.25 ppb (17%–68%) for ocean, and 0.28–0.77 ppb (23%–52%) for combined flux contributions. The observed seasonal amplitude ranges from 0.34 to 1.08 ppb for these sites. The stratospheric contributions to aN2O, inferred by the difference between the surface-troposphere model and observations, show 16%–126% larger amplitudes and minima delayed by ∼1 month compared to Northern Hemisphere site observations. Land fluxes and their seasonal amplitude have increased since the pre-industrial era and are projected to grow further under anthropogenic activities. Our results demonstrate the increasing importance of land fluxes for aN2O seasonality. Considering the large model spread, in situ aN2O observations and atmospheric transport-chemistry models will provide opportunities for constraining terrestrial and oceanic biosphere models, critical for projecting carbon-nitrogen cycles under ongoing global warming.

2024

PFAS Exposure is Associated with a Lower Spermatic Quality in an Arctic Seabird

Humann-Guilleminot, Ségolène; Blévin, Pierre; Gabrielsen, Geir W.; Herzke, Dorte; Nikiforov, Vladimir; Jouanneau, William; Moe, Børge; Parenteau, Charline; Helfenstein, Fabrice; Chastel, Olivier

Several studies have reported an increasing occurrence of poly- and perfluorinated alkyl substances (PFASs) in Arctic wildlife tissues, raising concerns due to their resistance to degradation. While some research has explored PFAS’s physiological effects on birds, their impact on reproductive functions, particularly sperm quality, remains underexplored. This study aims to assess (1) potential association between PFAS concentrations in blood and sperm quality in black-legged kittiwakes (Rissa tridactyla), focusing on the percentage of abnormal spermatozoa, sperm velocity, percentage of sperm motility, and morphology; and (2) examine the association of plasma levels of testosterone, corticosterone, and luteinizing hormone with both PFAS concentrations and sperm quality parameters to assess possible endocrine disrupting pathways. Our findings reveal a positive correlation between the concentration of longer-chain perfluoroalkyl carboxylates (PFCA; C11–C14) in blood and the percentage of abnormal sperm in kittiwakes. Additionally, we observed that two other PFAS (i.e., PFOSlin and PFNA), distinct from those associated with sperm abnormalities, were positively correlated with the stress hormone corticosterone. These findings emphasize the potentially harmful substance-specific effects of long-chain PFCAs on seabirds and the need for further research into the impact of pollutants on sperm quality as a potential additional detrimental effect on birds.

2024

Microplastics and nanoplastics in the marine-atmosphere environment

Allen, Deonie; Allen, Steve; Abbasi, Sajjad; Baker, Alex; Bergmann, Melanie; Brahney, Janice; Butler, Tim; Duce, Robert; Eckhardt, Sabine; Evangeliou, Nikolaos; Jickells, Tim; Kanakidou, Maria; Kershaw, Peter J; Laj, Paolo G.; Levermore, Joseph; Li, Daoji; Liss, Peter; Liu, Kai; Mahowald, Natalie M.; Masque, Pere; Materic, Dusan; Mayes, Andrew G.; McGinnity, Paul; Osvath, Iolanda; Prather, Kimberly A.; Prospero, Joseph M.; Revell, Laura E.; Sander, Sylvia G.; Shim, Won Joon; Slade, Jonathan; Stein, Ariel F.; Wright, Stephanie

The discovery of atmospheric micro(nano)plastic transport and ocean–atmosphere exchange points to a highly complex marine plastic cycle, with negative implications for human and ecosystem health. Yet, observations are currently limited. In this Perspective, we quantify the processes and fluxes of the marine-atmospheric micro(nano)plastic cycle, with the aim of highlighting the remaining unknowns in atmospheric micro(nano)plastic transport. Between 0.013 and 25 million metric tons per year of micro(nano)plastics are potentially being transported within the marine atmosphere and deposited in the oceans. However, the high uncertainty in these marine-atmospheric fluxes is related to data limitations and a lack of study intercomparability. To address the uncertainties and remaining knowledge gaps in the marine-atmospheric micro(nano)plastic cycle, we propose a future global marine-atmospheric micro(nano)plastic observation strategy, incorporating novel sampling methods and the creation of a comparable, harmonized and global data set. Together with long-term observations and intensive investigations, this strategy will help to define the trends in marine-atmospheric pollution and any responses to future policy and management actions.

2022

Revealing the significant acceleration of hydrofluorocarbon (HFC) emissions in eastern Asia through long-term atmospheric observations

Choi, Haklim; Redington, Alison L.; Park, Hyeri; Kim, Jooil; Thompson, Rona Louise; Mühle, Jens; Salameh, Peter K.; Harth, Christina M.; Weiss, Ray F.; Manning, Alistair J.; Park, Sunyoung

Hydrofluorocarbons (HFCs) are powerful anthropogenic greenhouse gases (GHGs) with high global-warming potentials (GWPs). They have been widely used as refrigerants, insulation foam-blowing agents, aerosol propellants, and fire suppression agents. Since the mid-1990s, emissions of HFCs have been increasing rapidly as they are used in many applications to replace ozone-depleting chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs) whose consumption and production have been phased out under the Montreal Protocol (MP). Due to the high GWP of HFCs, the Kigali Amendment to the MP requires the phasedown of production and consumption of HFCs to gradually achieve an 80 %–85 % reduction by 2047, starting in 2019 for non-Article 5 (developed) countries with a 10 % reduction against each defined baseline and later schedules for Article 5 (developing) countries. In this study, we have examined long-term high-precision measurements of atmospheric abundances of five major HFCs (HFC-134a, HFC-143a, HFC-32, HFC-125, and HFC-152a) at Gosan station, Jeju Island, South Korea, from 2008 to 2020. Background abundances of HFCs gradually increased, and the inflow of polluted air masses with elevated abundances from surrounding source regions were detected over the entire period. From these pollution events, we inferred regional and country-specific HFC emission estimates using two independent Lagrangian particle dispersion models and Bayesian inversion frameworks (FLEXPART-FLEXINVERT+ and NAME-InTEM). The spatial distribution of the derived “top-down” (measurement based) emissions for all HFCs shows large fluxes from megacities and industrial areas in the region. Our most important finding is that HFC emissions in eastern China and Japan have sharply increased from 2016 to 2018. The contribution of East Asian HFC emissions to the global total increased from 9 % (2008–2014) to 13 % (2016–2020). In particular, HFC emissions in Japan (Annex I country) rose rapidly from 2016 onward, with accumulated total inferred HFC emissions being ∼ 114 Gg yr−1, which is ∼ 76 Gg yr−1 higher for 2016–2020 than the “bottom-up” (i.e., based on activity data and emission factors) emissions of ∼ 38 Gg yr−1 reported to the United Nations Framework Convention on Climate Change (UNFCCC). This is likely related to the increase in domestic demand in Japan for refrigerants and air-conditioning-system-related products and incomplete accounting. A downward trend of HFC emissions that started in 2019 reflects the effectiveness of the F-gas policy in Japan. Eastern China and South Korea, though not obligated to report to the UNFCCC, voluntarily reported emissions, which also show differences between top-down and bottom-up emission estimates, demonstrating the need for atmospheric measurements, comprehensive data analysis, and accurate reporting for precise emission management. Further, the proportional contribution of each country's CO2-equivalent HFC emissions has changed over time, with HFC-134a decreasing and HFC-125 increasing. This demonstrates the transition in the predominant HFC substances contributing to global warming in each country.

2024

Technical and environmental viability of a European CO2 EOR system

Thorne, Rebecca Jayne; Sundseth, Kyrre; Bouman, Evert; Czarnowska, Lucyna; Mathisen, Anette; Skagestad, Ragnhild; Stanek, Wojciech; Pacyna, Jozef M; Pacyna, Elisabeth G

Captured CO2 from large industrial emitters may be used for enhanced oil recovery (EOR), but as of yet there are no European large-scale EOR systems. Recent implementation decisions for a Norwegian carbon capture and storage demonstration will result in the establishment of a central CO2 hub on the west-coast of Norway and storage on the Norwegian Continental Shelf. This development may continue towards a large-scale operation involving European CO2 and CO2 EOR operation. To this end, a conceptual EOR system was developed here based on an oxyfuel power plant located in Poland that acted as a source for CO2, coupled to a promising oil field located on the Norwegian Continental Shelf. Lifecycle assessment was subsequently used to estimate environmental emissions indicators. When averaged over the operational lifetime, results show greenhouse gas (GHG) emissions of 0.4 kg CO2-eq per kg oil (and n kWh associated electricity) produced, of which 64 % derived from the oxyfuel power plant. This represents a 71 % emission reduction when compared to the same amount of oil and electricity production using conventional technology. Other environmental impact indicators were increased, showing that this type of CO2 EOR system may help reach GHG reduction targets, but care should be taken to avoid problem shifting.

2020

Time trends of persistent organic pollutants in 30 year olds sampled in 1986, 1994, 2001 and 2007 in Northern Norway: measurements, mechanistic modeling and a comparison of study designs

Nøst, Therese Haugdahl; Berg, Vivian; Hanssen, Linda; Rylander, Charlotta; Gaudreau, Eric; Dumas, Pierre; Breivik, Knut; Sandanger, Torkjel M

<p><i>Background</i>: Human biomonitoring studies have demonstrated decreasing concentrations of many persistent organic pollutants (POPs) in years after emission peaks.</p> <p><i>Objectives</i>: To describe time trends of POPs in blood using four cross-sectional samples of 30 year olds from Tromsø, Norway across 1986–2007, and to compare the measured concentrations of polychlorinated biphenyl 153 (PCB-153) to model-estimated values. A second objective was to compare the repeated cross-sectional time trends with those observed in our previous longitudinal study using repeated individual measurements in older men from the same surveys.</p> <p><i>Methods</i>: Serum from 45 persons aged 30 years in each of the following years: 1986, 1994, 2001, and 2007 was analyzed for 14 POPs. Further, predicted concentrations of PCB-153 in each sampling year were derived using the emission-based CoZMoMAN model.</p> <p><i>Results</i>: The median decreases in summed serum POP concentrations (lipid-adjusted) in 1994, 2001, and 2007 relative to 1986 were − 71%, − 81%, and − 86% for women and − 65%, − 77%, and − 87% for men, respectively. The overall time trend in predicted PCB-153 concentrations demonstrated agreement with the observed trend although model predictions were higher than the measured concentrations at all time points. Compared to our previous longitudinal study of repeated individual measurements in older men, similar although more prominent declines were observed in the younger cross-sectional samples.</p> <p><i>Discussion</i>: Observed declines in serum concentrations from 1986 to 2007 were substantial for legacy POPs in men and women at reproductive ages in Northern Norway and are generally consistent with previous longitudinal biomonitoring efforts in the study population. The measured concentrations and observed declines likely reflect a combination of recent and historic exposures. Small differences in time trends observed between the studies could be attributed to different study designs (i.e. the chosen age group or sex and cross-sectional versus repeated individual measurement sampling).</p>

2019

Temporal and cross-sectional associations of serum per- and polyfluoroalkyl substances (PFAS) and lipids from 1986 to 2016 − The Tromsø study

Coelho, Ana Carolina; Charles, Dolley; Nøst, Therese Haugdahl; Cioni, Lara; Huber, Sandra; Herzke, Dorte; Rylander, Charlotta; Berg, Vivian; Sandanger, Torkjel M

Introduction
Per- and polyfluoroalkyl substances (PFAS) have been linked to effects on human lipid profiles, with several epidemiological studies reporting associations between specific PFAS and blood lipid concentrations. However, these associations have been inconsistent, and most studies have focused on cross-sectional analyses with limited repeated measurements.

Objective
In this study, we investigated associations between serum PFAS concentrations and major blood lipid classes over a 30-year period (1986–2016) and up to five time points. Lipids analyzed included total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides (TG).

Methods
This study included 145 participants from The Tromsø Study, Norway, who donated plasma samples three to five times over the study period. Linear mixed-effects (LME) models assessed longitudinal associations between PFAS and lipid classes, while multiple linear regression (MLR) models were used for cross-sectional associations.

Results
LME models demonstrated positive longitudinal associations between perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnDA), perfluorododecanoic acid (PFDoDA), and perfluorotridecanoic acid (PFTrDA) with TC. Additionally, PFOA, PFDA, PFUnDA, PFDoDA, and PFTrDA were associated with LDL-C, and PFUnDA and summed perfluorooctane sulfonate isomers (∑PFOS) with HDL-C. Cross-sectional analyses corroborated positive associations between the six PFAS compounds and TC at least three times, but the LDL-C and HDL-C associations were not confirmed. Summed perfluorooctane sulfonamide isomers (∑PFOSA) showed a negative association with LDL-C longitudinally, but this was not confirmed cross-sectionally. No associations were observed between PFAS and TG, longitudinally or cross-sectionally.

Conclusion
Concentrations of multiple PFAS were positively associated with blood lipids in longitudinal analyses, with the most consistent associations observed between six PFCA compounds and TC. These findings highlight the need for further investigation into these complex associations.

2025

Webcrawling and machine learning as a new approach for the spatial distribution of atmospheric emissions

Lopez-Aparicio, Susana; Grythe, Henrik; Vogt, Matthias; Pierce, Matthew; Vallejo, Islen

In this study we apply two methods for data collection that are relatively new in the field of atmospheric science. The two developed methods are designed to collect essential geo-localized information to be used as input data for a high resolution emission inventory for residential wood combustion (RWC). The first method is a webcrawler that extracts openly online available real estate data in a systematic way, and thereafter structures them for analysis. The webcrawler reads online Norwegian real estate advertisements and it collects the geo-position of the dwellings. Dwellings are classified according to the type (e.g., apartment, detached house) they belong to and the heating systems they are equipped with. The second method is a model trained for image recognition and classification based on machine learning techniques. The images from the real estate advertisements are collected and processed to identify wood burning installations, which are automatically classified according to the three classes used in official statistics, i.e., open fireplaces, stoves produced before 1998 and stoves produced after 1998. The model recognizes and classifies the wood appliances with a precision of 81%, 85% and 91% for open fireplaces, old stoves and new stoves, respectively. Emission factors are heavily dependent on technology and this information is therefore essential for determining accurate emissions. The collected data are compared with existing information from the statistical register at county and national level in Norway. The comparison shows good agreement for the proportion of residential heating systems between the webcrawled data and the official statistics. The high resolution and level of detail of the extracted data show the value of open data to improve emission inventories. With the increased amount and availability of data, the techniques presented here add significant value to emission accuracy and potential applications should also be considered across all emission sectors.

2018

Are Fluoropolymers Really of Low Concern for Human and Environmental Health and Separate from Other PFAS?

Lohmann, Rainer; Cousins, Ian T.; DeWitt, Jamie; Glüge, Juliane; Goldenman, Gretta; Herzke, Dorte; Lindstrom, Andrew B.; Miller, Mark F.; Ng, Carla A.; Patton, Sharyle; Scheringer, Martin; Trier, Xenia; Wang, Zhanyun

Fluoropolymers are a group of polymers within the class of per- and polyfluoroalkyl substances (PFAS). The objective of this analysis is to evaluate the evidence regarding the environmental and human health impacts of fluoropolymers throughout their life cycle(s). Production of some fluoropolymers is intimately linked to the use and emissions of legacy and novel PFAS as polymer processing aids. There are serious concerns regarding the toxicity and adverse effects of fluorinated processing aids on humans and the environment. A variety of other PFAS, including monomers and oligomers, are emitted during the production, processing, use, and end-of-life treatment of fluoropolymers. There are further concerns regarding the safe disposal of fluoropolymers and their associated products and articles at the end of their life cycle. While recycling and reuse of fluoropolymers is performed on some industrial waste, there are only limited options for their recycling from consumer articles. The evidence reviewed in this analysis does not find a scientific rationale for concluding that fluoropolymers are of low concern for environmental and human health. Given fluoropolymers’ extreme persistence; emissions associated with their production, use, and disposal; and a high likelihood for human exposure to PFAS, their production and uses should be curtailed except in cases of essential uses.

2020

Temporal variability in surface water pCO2 in Adventfjorden (West Spitsbergen) with emphasis on physical and biogeochemical drivers

Ericson, Ylva; Falck, Eva; Chierici, Melissa; Fransson, Agneta Ingrid; Kristiansen, Svein; Platt, Stephen Matthew; Hermansen, Ove; Myhre, Cathrine Lund

Seasonal and interannual variability in surface water partial pressure of CO2 (pCO2) and air‐sea CO2 fluxes from a West Spitsbergen fjord (IsA Station, Adventfjorden) are presented, and the associated driving forces are evaluated. Marine CO2 system data together with temperature, salinity, and nutrients, were collected at the IsA Station between March 2015 and June 2017. The surface waters were undersaturated in pCO2 with respect to atmospheric pCO2 all year round. The effects of biological activity (primary production/respiration) followed by thermal forcing on pCO2 were the most important drivers on a seasonal scale. The ocean was a sink for atmospheric CO2 with annual air‐sea CO2 fluxes of −36 ± 2 and −31 ± 2 g C·m−2·year−1 for 2015–2016 and 2016–2017, respectively, as estimated from the month of April. Waters of an Arctic origin dominated in 2015 and were replaced in 2016 by waters of a transformed Atlantic source. The CO2 uptake rates over the period of Arctic origin waters were significantly higher (2 mmol C·m−2·day−1) than the rates of the Atlantic origin waters of the following year.

2018

Sources and Seasonal Variations of Per- and Polyfluoroalkyl Substances (PFAS) in Surface Snow in the Arctic

Hartz, William Frederik; Björnsdotter, Maria; Yeung, Leo W. Y.; Humby, Jack D.; Eckhardt, Sabine; Evangeliou, Nikolaos; Jogsten, Ingrid Ericson; Kärrman, Anna; Kallenborn, Roland

Per- and polyfluoroalkyl substances (PFAS) are persistent anthropogenic contaminants, some of which are toxic and bioaccumulative. Perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs) can form during the atmospheric degradation of precursors such as fluorotelomer alcohols (FTOHs), N-alkylated perfluoroalkane sulfonamides (FASAs), and hydrofluorocarbons (HFCs). Since PFCAs and PFSAs will readily undergo wet deposition, snow and ice cores are useful for studying PFAS in the Arctic atmosphere. In this study, 36 PFAS were detected in surface snow around the Arctic island of Spitsbergen during January–August 2019 (i.e., 24 h darkness to 24 h daylight), indicating widespread and chemically diverse contamination, including at remote high elevation sites. Local sources meant some PFAS had concentrations in snow up to 54 times higher in Longyearbyen, compared to remote locations. At a remote high elevation ice cap, where PFAS input was from long-range atmospheric processes, the median deposition fluxes of C2–C11 PFCAs, PFOS and HFPO–DA (GenX) were 7.6–71 times higher during 24 h daylight. These PFAS all positively correlated with solar flux. Together this suggests seasonal light is important to enable photochemistry for their atmospheric formation and subsequent deposition in the Arctic. This study provides the first evidence for the possible atmospheric formation of PFOS and GenX from precursors.

2024

Climate change rivals fertilizer use in driving soil nitrous oxide emissions in the northern high latitudes: Insights from terrestrial biosphere models

Pan, Naiqing; Tian, Hanqin; Shi, Hao; Pan, Shufen; Canadell, Josep G.; Chang, Jinfeng; Ciais, Philippe; Davidson, Eric A.; Hugelius, Gustaf; Ito, Akihiko; Jackson, Robert B.; Joos, Fortunat; Lienert, Sebastian; Millet, Dylan B.; Olin, Stefan; Patra, Prabir K.; Thompson, Rona Louise; Vuichard, Nicolas; Wells, Kelley C.; Wilson, Chris; You, Yongfa; Zaehle, Sönke

Nitrous oxide (N2O) is the most important stratospheric ozone-depleting agent based on current emissions and the third largest contributor to increased net radiative forcing. Increases in atmospheric N2O have been attributed primarily to enhanced soil N2O emissions. Critically, contributions from soils in the Northern High Latitudes (NHL, >50°N) remain poorly quantified despite their exposure to rapid rates of regional warming and changing hydrology due to climate change. In this study, we used an ensemble of six process-based terrestrial biosphere models (TBMs) from the Global Nitrogen/Nitrous Oxide Model Intercomparison Project (NMIP) to quantify soil N2​O emissions across the NHL during 1861–2016. Factorial simulations were conducted to disentangle the contributions of key driving factors, including climate change, nitrogen inputs, land use change, and rising atmospheric CO2 concentration​, to the trends in emissions. The NMIP models suggests NHL soil N2O emissions doubled from 1861 to 2016, increasing on average by 2.0 ± 1.0 Gg N/yr (p

2025

Total ozone trends at three northern high-latitude stations

Bernet, Leonie; Svendby, Tove Marit; Hansen, Georg Heinrich; Orsolini, Yvan; Dahlback, Arne; Goutail, Florence; Pazmino, Andrea; Petkov, Boyan; Kylling, Arve

After the decrease of ozone-depleting substances (ODSs) as a consequence of the Montreal Protocol, it is still challenging to detect a recovery in the total column amount of ozone (total ozone) at northern high latitudes. To assess regional total ozone changes in the “ozone-recovery” period (2000–2020) at northern high latitudes, this study investigates trends from ground-based total ozone measurements at three stations in Norway (Oslo, Andøya, and Ny-Ålesund). For this purpose, we combine measurements from Brewer spectrophotometers, ground-based UV filter radiometers (GUVs), and a SAOZ (Système d'Analyse par Observation Zénithale) instrument. The Brewer measurements have been extended to work under cloudy conditions using the global irradiance (GI) technique, which is also presented in this study. We derive trends from the combined ground-based time series with the multiple linear regression model from the Long-term Ozone Trends and Uncertainties in the Stratosphere (LOTUS) project. We evaluate various predictors in the regression model and found that tropopause pressure and lower-stratospheric temperature contribute most to ozone variability at the three stations. We report significantly positive annual trends at Andøya (0.9±0.7 % per decade) and Ny-Ålesund (1.5±0.1 % per decade) and no significant annual trend at Oslo (0.1±0.5 % per decade) but significantly positive trends in autumn at all stations. Finally we found positive but insignificant trends of around 3 % per decade in March at all three stations, which may be an indication of Arctic springtime ozone recovery. Our results contribute to a better understanding of regional total ozone trends at northern high latitudes, which is essential to assess how Arctic ozone responds to changes in ODSs and to climate change.

2023

Mass Cultivation of Microalgae: I. Experiences with Vertical Column Airlift Photobioreactors, Diatoms and CO2 Sequestration

Eilertsen, Hans Christian; Eriksen, Gunilla; Bergum, John-Steinar; Strømholt, Jo; Elvevoll, Edel O.; Eilertsen, Karl-Erik; Heimstad, Eldbjørg Sofie; Giæver, Ingeborg Hulda; Israelsen, Linn; Svenning, Jon Brage; Dalheim, Lars; Osvik, Renate Døving; Hansen, Espen Holst; Ingebrigtsen, Richard Andre; Aspen, Terje M; Wintervoll, Geir-Henning

From 2015 to 2021, we optimized mass cultivation of diatoms in our own developed vertical column airlift photobioreactors using natural and artificial light (LEDs). The project took place at the ferrosilicon producer Finnfjord AS in North Norway as a joint venture with UiT—The Arctic University of Norway. Small (0.1–6–14 m3) reactors were used for initial experiments and to produce inoculum cultures while upscaling experiments took place in a 300 m3 reactor. We here argue that species cultivated in reactors should be large since biovolume specific self-shadowing of light can be lower for large vs. small cells. The highest production, 1.28 cm3 L−1 biovolume (0.09–0.31 g DW day−1), was obtained with continuous culture at ca. 19% light utilization efficiency and 34% CO2 uptake. We cultivated 4–6 months without microbial contamination or biofouling, and this we argue was due to a natural antifouling (anti-biofilm) agent in the algae. In terms of protein quality all essential amino acids were present, and the composition and digestibility of the fatty acids were as required for feed ingredients. Lipid content was ca. 20% of ash-free DW with high EPA levels, and omega-3 and amino acid content increased when factory fume was added. The content of heavy metals in algae cultivated with fume was well within the accepted safety limits. Organic pollutants (e.g., dioxins and PCBs) were below the limits required by the European Union food safety regulations, and bioprospecting revealed several promising findings.

2022

An Introduction to prismAId: Open-Source and Open Science AI for Advancing Information Extraction in Systematic Reviews

Boero, Riccardo

prismAId is an open-source tool designed to streamline systematic literature reviews by leveraging generative AI models for information extraction. It offers an accessible, efficient, and replicable method for extracting and analyzing data from scientific literature, eliminating the need for coding expertise. Supporting various review protocols, including PRISMA 2020, prismAId is distributed across multiple platforms – Go, Python, Julia, R – and provides user-friendly binaries compatible with Windows, macOS, and Linux. The tool integrates with leading large language models (LLMs) such as OpenAI’s GPT series, Google’s Gemini, Cohere’s Command, and Anthropic’s Claude, ensuring comprehensive and up-to-date literature analysis. prismAId facilitates systematic reviews, enabling researchers to conduct thorough, fast, and reproducible analyses, thereby advancing open science initiatives.

2025

Titanium dioxide nanoparticles tested for genotoxicity with the comet and micronucleus assays in vitro, ex vivo and in vivo

Kazimirova, Alena; Baranokova, Magdalena; Staruchova, Marta; Drlickova, Martina; Volkovova, Katarina; Dusinska, Maria

2019

Understanding thermal comfort expectations in older adults: The role of long-term thermal history

Hassani, Amirhossein; Jancewicz, Barbara; Wrotek, Malgorzata; Chwałczyk, Franciszek; Castell, Nuria

Understanding how long-term thermal history affects thermal comfort expectations in older adults (65+) has implications for designing energy-efficient spaces in a changing climate. A growing number of studies focus on thermal sensation/preference votes to represent the current thermal comfort expectations, often overlooking their limitations. This study, however, investigates how factors shaping long-term thermal history link to the current 65+ adults indoor thermal comfort expectations during exposure to heat, by focusing on the upper limit of thermally acceptable temperature range, represented by a self-reported temperature threshold at which 65+ adults believe to feel uncomfortable by indoor heat (Tit). To find Tit, we use answers to “Above what temperature do you start feeling too hot indoors?” by survey respondents in Warsaw (n = 678) and Madrid (n = 527), who lived in their apartment ≥5 years. Statistically, we find indoor factors affecting long-term thermal experiences more significant in explaining 65+ Tit, when compared to outdoor factors such as distance to water, vegetation, or surface thermal radiance. Better-insulated buildings were associated with a lower Tit [...]

2024

On the Convergence and Capability of the Large-Eddy Simulation of Concentration Fluctuations in Passive Plumes for a Neutral Boundary Layer at Infinite Reynolds Number

Ardeshiri, Hamidreza; Cassiani, Massimo; Park, Soon-Young; Stohl, Andreas; Pisso, Ignacio; Dinger, Anna Solvejg

Large-eddy simulation (LES) experiments have been performed using the Parallelized LES Model (PALM). A methodology for validating and understanding LES results for plume dispersion and concentration fluctuations in an atmospheric-like flow is presented. A wide range of grid resolutions is shown to be necessary for investigating the convergence of statistical characteristics of velocity and scalar fields. For the scalar, the statistical moments up to the fourth order and the shape of the concentration probability density function (p.d.f.) are examined. The mean concentration is influenced by grid resolution, with the highest resolution simulation showing a lower mean concentration, linked to larger turbulent structures. However, a clear tendency to convergence of the concentration variance is observed at the two higher resolutions. This behaviour is explained by showing that the mechanisms driving the mean and the variance are differently influenced by the grid resolution. The analysis of skewness and kurtosis allows also the obtaining of general results on plume concentration fluctuations. Irrespective of grid resolution, a family of Gamma p.d.f.s well represents the shape of the concentration p.d.f. but only beyond the peak of the concentration fluctuation intensity. In the early plume dispersion phases, the moments of the p.d.f. are in good agreement with those generated by a fluctuating plume model. To the best of our knowledge, our study demonstrates for the first time that, if resolution and averaging time are adequate, atmospheric LES provides a trustworthy representation of the high order moments of the concentration field, up to the fourth order, for a dispersing plume.

2020

Car Tire Crumb Rubber: Does Leaching Produce a Toxic Chemical Cocktail in Coastal Marine Systems?

Halsband-Lenk, Claudia; Sørensen, Lisbet; Booth, Andy; Herzke, Dorte

Crumb rubber granulate (CRG) produced from end of life tires (ELTs) is commonly applied to synthetic turf pitches (STPs), playgrounds, safety surfaces and walkways. In addition to fillers, stabilizers, cross-linking agents and secondary components (e.g., pigments, oils, resins), ELTs contain a range of other organic compound and heavy metal additives. While previous environmental impact studies on CRG have focused on terrestrial soil and freshwater ecosystems, many sites applying CRG in Norway are coastal. The current study investigated the organic chemical and metal additive content of ‘pristine’ and ‘weathered’ CRG and their seawater leachates, as well as uptake and effects of leachate exposure using marine copepods (Acartia and Calanus sp.). A combination of pyrolysis gas chromatography mass spectrometry (py-GC-MS) and chemical extraction followed by GC-MS analysis revealed similar organic chemical profiles for pristine and weathered CRG, including additives such as benzothiazole, N-1,3-dimethylbutyl-N′-phenyl-p-phenylenediamine and a range of polycyclic aromatic hydrocarbons (PAHs) and phenolic compounds (e.g., bisphenols). ICP-MS analysis revealed g kg–1 quantities of Zn and mg kg–1 quantities of Fe, Mn, Cu, Co, Cr, Pb, and Ni in the CRG. A cocktail of organic additives and metals readily leached from the CRG into seawater, with the most abundant leachate components being benzothiazole and Zn, Fe, Co (metals), as well as detectable levels of PAHs and phenolic compounds. Concentrations of individual components varied with CRG source material and CRG to seawater ratio, but benzothiazole and Zn were typically the organic and metal components present at the highest concentrations in the leachates. While organic chemical concentrations in the leachates stabilized within days, metals continued to leach out over the 30-day period. Marine copepods exposed to high CRG leachate concentrations exhibited high mortalities within 48 h. The smaller lipid-poor Acartia had a higher sensitivity to leachates than the larger lipid-rich Calanus, indicating species-specific differences in vulnerability to leachates. The effect on survival was alleviated at lower leachate concentrations, indicating a dose-response relationship. Benzothiazole and its derivatives appear to be of concern owing to their proven toxicity, while bisphenols are also known to be toxic and were enriched in the leachates relative to the other compounds in the CRG.

2020

Legacy and emerging per- and polyfluoroalkyl substances in eggs of yellow-legged gulls from Southern France

Jouanneau, William; Boulinier, Thierry; Herzke, Dorte; Nikiforov, Vladimir; Gabrielsen, Geir Wing; Chastel, Olivier

More than 70 years of industrial production of per- and polyfluoroalkyl substances (PFAS) have resulted in their ubiquitous presence in the environment on a global scale, although differences in sources, transport and fate lead to variability of occurrence in the environment. Gull eggs are excellent bioindicators of environmental pollution, especially for persistent organic pollutants such as PFAS, known to bioaccumulate in organisms and to be deposited in bird eggs by maternal transfer. Using yellow-legged gull (Larus michahellis) eggs, we investigated the occurrence of more than 30 PFAS, including the most common chemicals (i.e., legacy PFAS) as well as their alternatives (i.e., emerging PFAS) in the Bay of Marseille, the second largest city in France. Compared to eggs from other colonies along the Mediterranean coast, those from Marseille had PFAS concentrations ranging from slightly higher to up to four times lower, suggesting that this area cannot be specifically identified as a hotspot for these compounds. We also found several emerging PFAS including 8:2 and 10:2 FTS, 7:3 FTCA or PFECHS in all collected eggs. Although the scarcity in toxicity thresholds for seabirds, especially during embryogenesis, does not enable any precise statement about the risks faced by this population, this study contributes to the effort in documenting legacy PFAS contamination on Mediterranean coasts while providing valuable novel inputs on PFAS of emerging concern. Identifying exposure in free-ranging species also participate to determine the main target for toxicity testing in wildlife.

2025

The urban dispersion model EPISODE v10.0 – Part 1: An Eulerian and sub-grid-scale air quality model and its application in Nordic winter conditions

Hamer, Paul David; Walker, Sam-Erik; Santos, Gabriela Sousa; Vogt, Matthias; Vo, Dam Thanh; Lopez-Aparicio, Susana; Schneider, Philipp; Ramacher, Martin O. P.; Karl, Matthias

This paper describes the Eulerian urban dispersion model EPISODE. EPISODE was developed to address a need for an urban air quality model in support of policy, planning, and air quality management in the Nordic, specifically Norwegian, setting. It can be used for the calculation of a variety of airborne pollutant concentrations, but we focus here on the implementation and application of the model for NO2 pollution. EPISODE consists of an Eulerian 3D grid model with embedded sub-grid dispersion models (e.g. a Gaussian plume model) for dispersion of pollution from line (i.e. roads) and point sources (e.g. chimney stacks). It considers the atmospheric processes advection, diffusion, and an NO2 photochemistry represented using the photostationary steady-state approximation for NO2. EPISODE calculates hourly air concentrations representative of the grids and at receptor points. The latter allow EPISODE to estimate concentrations representative of the levels experienced by the population and to estimate their exposure. This methodological framework makes it suitable for simulating NO2 concentrations at fine-scale resolution (<100 m) in Nordic environments. The model can be run in an offline nested mode using output concentrations from a global or regional chemical transport model and forced by meteorology from an external numerical weather prediction model; it also can be driven by meteorological observations. We give a full description of the overall model function and its individual components. We then present a case study for six Norwegian cities whereby we simulate NO2 pollution for the entire year of 2015. The model is evaluated against in situ observations for the entire year and for specific episodes of enhanced pollution during winter. We evaluate the model performance using the FAIRMODE DELTA Tool that utilises traditional statistical metrics, e.g. root mean square error (RMSE), Pearson correlation R, and bias, along with some specialised tests for air quality model evaluation. We find that EPISODE attains the DELTA Tool model quality objective in all of the stations we evaluate against. Further, the other statistical evaluations show adequate model performance but that the model scores greatly improved correlations during winter and autumn compared to the summer. We attribute this to the use of the photostationary steady-state scheme for NO2, which should perform best in the absence of local ozone photochemical production. Oslo does not comply with the NO2 annual limit set in the 2008/50/EC directive (AQD). NO2 pollution episodes with the highest NO2 concentrations, which lead to the occurrence of exceedances of the AQD hourly limit for NO2, occur primarily in the winter and autumn in Oslo, so this strongly supports the use of EPISODE for application to these wintertime events. Overall, we conclude that the model is suitable for an assessment of annual mean NO2 concentrations and also for the study of hourly NO2 concentrations in the Nordic winter and autumn environment. Further, in this work we conclude that it is suitable for a range of policy applications specific to NO2 that include pollution episode analysis, evaluation of seasonal statistics, policy and planning support, and air quality management. Lastly, we identify a series of model developments specifically designed to address the limitations of the current model assumptions. Part 2 of this two-part paper discusses the CityChem extension to EPISODE, which includes a number of implementations such as a more comprehensive photochemical scheme suitable for describing more chemical species and a more diverse range of photochemical environments, as well as a more advanced treatment of the sub-grid dispersion.

2020

Spatiotemporal Patterns in Data Availability of the Sentinel-5P NO2 Product over Urban Areas in Norway

Schneider, Philipp; Hamer, Paul David; Kylling, Arve; Shetty, Shobitha; Stebel, Kerstin

Due to its comparatively high spatial resolution and its daily repeat frequency, the tropospheric nitrogen dioxide product provided by the TROPOspheric Monitoring Instrument (TROPOMI) onboard the Sentinel-5 Precursor platform has attracted significant attention for its potential for urban-scale monitoring of air quality. However, the exploitation of such data in, for example, operational assimilation of local-scale dispersion models is often complicated by substantial data gaps due to cloud cover or other retrieval limitations. These challenges are particularly prominent in high-latitude regions where significant cloud cover and high solar zenith angles are often prevalent. Using the example of Norway as a representative case for a high-latitude region, we here evaluate the spatiotemporal patterns in the availability of valid data from the operational TROPOMI tropospheric nitrogen dioxide (NO2) product over five urban areas (Oslo, Bergen, Trondheim, Stavanger, and Kristiansand) and a 2.5 year period from July 2018 through November 2020. Our results indicate that even for relatively clean environments such as small Norwegian cities, distinct spatial patterns of tropospheric NO2 are visible in long-term average datasets from TROPOMI. However, the availability of valid data on a daily level is limited by both cloud cover and solar zenith angle (during the winter months), causing the fraction of valid retrievals in each study site to vary from 20% to 50% on average. A temporal analysis shows that for our study sites and the selected period, the fraction of valid pixels in each domain shows a clear seasonal cycle reaching a maximum of 50% to 75% in the summer months and 0% to 20% in winter. The seasonal cycle in data availability shows the inverse behavior of NO2 pollution in Norway, which typically has its peak in the winter months. However, outside of the mid-winter period we find the TROPOMI NO2 product to provide sufficient data availability for detailed mapping and monitoring of NO2 pollution in the major urban areas in Norway and see potential for the use of the data in local-scale data assimilation and emission inversions applications.

2021

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