Found 2647 publications. Showing page 50 of 265:
Microfibers (MF) are one of the major classes of microplastic found in the marine environment on a global scale. Very little is known about how they move and distribute from point sources such as wastewater effluents into the ocean. We chose Adventfjorden near the settlement of Longyearbyen on the Arctic Svalbard archipelago as a case study to investigate how microfibers emitted with untreated wastewater will distribute in the fjord, both on a spatial and temporal scale. Fiber abundance in the effluent was estimated from wastewater samples taken during two one-week periods in June and September 2017. Large emissions of MFs were detected, similar in scale to a modern WWTP serving 1.3 million people and providing evidence of the importance of untreated wastewater from small settlements as major local sources for MF emissions in the Arctic. Fiber movement and distribution in the fjord mapped using an online-coupled hydrodynamic-drift model (FVCOM-FABM). For parameterizing a wider spectrum of fibers from synthetic to wool, four different density classes of MFs, i.e., buoyant, neutral, sinking, and fast sinking fibers are introduced to the modeling framework. The results clearly show that fiber class has a large impact on the fiber distributions. Light fibers remained in the surface layers and left the fjord quickly with outgoing currents, while heavy fibers mostly sank to the bottom and deposited in the inner parts of the fjord and along the northern shore. A number of accumulation sites were identified within the fjord. The southern shore, in contrast, was much less affected, with low fiber concentrations throughout the modeling period. Fiber distributions were then compared with published pelagic and benthic fauna distributions in different seasons at selected stations around the fjord. The ratios of fibers to organisms showed a very wide range, indicating hot spots of encounter risk for pelagic and benthic biota. This approach, in combination with in-situ ground-truthing, can be instrumental in understanding microplastic pathways and fate in fjord systems and coastal areas and help authorities develop monitoring and mitigation strategies for microfiber and microplastic pollution in their local waters.
Frontiers Media S.A.
2021
2021
Paris Agreement. This study provides a consolidated synthesis of estimates for all anthropogenic and natural sources and sinks of CO2 for the European Union and UK (EU27 + UK), derived from a combination of state-of-the-art bottom-up (BU) and top-down (TD) data sources and models. Given the wide scope of the work and the variety of datasets involved, this study focuses on identifying essential questions which need to be answered to properly understand the differences between various datasets, in particular with regards to the less-well-characterized fluxes from managed ecosystems. The work integrates recent emission inventory data, process-based ecosystem model results, data-driven sector model results and inverse modeling estimates over the period 1990–2018. BU and TD products are compared with European national greenhouse gas inventories (NGHGIs) reported under the UNFCCC in 2019, aiming to assess and understand the differences between approaches. For the uncertainties in NGHGIs, we used the standard deviation obtained by varying parameters of inventory calculations, reported by the member states following the IPCC Guidelines. Variation in estimates produced with other methods, like atmospheric inversion models (TD) or spatially disaggregated inventory datasets (BU), arises from diverse sources including within-model uncertainty related to parameterization as well as structural differences between models. In comparing NGHGIs with other approaches, a key source of uncertainty is that related to different system boundaries and emission categories (CO2 fossil) and the use of different land use definitions for reporting emissions from land use, land use change and forestry (LULUCF) activities (CO2 land). At the EU27 + UK level, the NGHGI (2019) fossil CO2 emissions (including cement production) account for 2624 Tg CO2 in 2014 while all the other seven bottom-up sources are consistent with the NGHGIs and report a mean of 2588 (± 463 Tg CO2). The inversion reports 2700 Tg CO2 (± 480 Tg CO2), which is well in line with the national inventories. Over 2011–2015, the CO2 land sources and sinks from NGHGI estimates report −90 Tg C yr−1 ± 30 Tg C yr−1 while all other BU approaches report a mean sink of −98 Tg C yr−1 (± 362 Tg of C from dynamic global vegetation models only). For the TD model ensemble results, we observe a much larger spread for regional inversions (i.e., mean of 253 Tg C yr−1 ± 400 Tg C yr−1). This concludes that (a) current independent approaches are consistent with NGHGIs and (b) their uncertainty is too large to allow a verification because of model differences and probably also because of the definition of “CO2 flux” obtained from different approaches. The referenced datasets related to figures are visualized at https://doi.org/10.5281/zenodo.4626578 (Petrescu et al., 2020a).
2021
Reliable quantification of the sources and sinks of greenhouse gases, together with trends and uncertainties, is essential to monitoring the progress in mitigating anthropogenic emissions under the Paris Agreement. This study provides a consolidated synthesis of CH4 and N2O emissions with consistently derived state-of-the-art bottom-up (BU) and top-down (TD) data sources for the European Union and UK (EU27 + UK). We integrate recent emission inventory data, ecosystem process-based model results and inverse modeling estimates over the period 1990–2017. BU and TD products are compared with European national greenhouse gas inventories (NGHGIs) reported to the UN climate convention UNFCCC secretariat in 2019. For uncertainties, we used for NGHGIs the standard deviation obtained by varying parameters of inventory calculations, reported by the member states (MSs) following the recommendations of the IPCC Guidelines. For atmospheric inversion models (TD) or other inventory datasets (BU), we defined uncertainties from the spread between different model estimates or model-specific uncertainties when reported. In comparing NGHGIs with other approaches, a key source of bias is the activities included, e.g., anthropogenic versus anthropogenic plus natural fluxes. In inversions, the separation between anthropogenic and natural emissions is sensitive to the geospatial prior distribution of emissions. Over the 2011–2015 period, which is the common denominator of data availability between all sources, the anthropogenic BU approaches are directly comparable, reporting mean emissions of 20.8 Tg CH4 yr−1 (EDGAR v5.0) and 19.0 Tg CH4 yr−1 (GAINS), consistent with the NGHGI estimates of 18.9 ± 1.7 Tg CH4 yr−1. The estimates of TD total inversions give higher emission estimates, as they also include natural emissions. Over the same period regional TD inversions with higher-resolution atmospheric transport models give a mean emission of 28.8 Tg CH4 yr−1. Coarser-resolution global TD inversions are consistent with regional TD inversions, for global inversions with GOSAT satellite data (23.3 Tg CH4 yr−1) and surface network (24.4 Tg CH4 yr−1). The magnitude of natural peatland emissions from the JSBACH–HIMMELI model, natural rivers and lakes emissions, and geological sources together account for the gap between NGHGIs and inversions and account for 5.2 Tg CH4 yr−1. For N2O emissions, over the 2011–2015 period, both BU approaches (EDGAR v5.0 and GAINS) give a mean value of anthropogenic emissions of 0.8 and 0.9 Tg N2O yr−1, respectively, agreeing with the NGHGI data (0.9 ± 0.6 Tg N2O yr−1). Over the same period, the average of the three total TD global and regional inversions was 1.3 ± 0.4 and 1.3 ± 0.1 Tg N2O yr−1, respectively. The TD and BU comparison method defined in this study can be operationalized for future yearly updates for the calculation of CH4 and N2O budgets both at the EU+UK scale and at the national scale. The referenced datasets related to figures are visualized at https://doi.org/10.5281/zenodo.4590875 (Petrescu et al., 2020b)
2021
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.
MDPI
2021
Measurements of total ozone column and effective cloud transmittance have been performed since 1995 at the three Norwegian sites Oslo/Kjeller, Andøya/Tromsø, and in Ny-Ålesund (Svalbard). These sites are a subset of nine stations included in the Norwegian UV monitoring network, which uses ground-based ultraviolet (GUV) multi-filter instruments and is operated by the Norwegian Radiation and Nuclear Safety Authority (DSA) and the Norwegian Institute for Air Research (NILU). The network includes unique data sets of high-time-resolution measurements that can be used for a broad range of atmospheric and biological exposure studies. Comparison of the 25-year records of GUV (global sky) total ozone measurements with Brewer direct sun (DS) measurements shows that the GUV instruments provide valuable supplements to the more standardized ground-based instruments. The GUV instruments can fill in missing data and extend the measuring season at sites with reduced staff and/or characterized by harsh environmental conditions, such as Ny-Ålesund. Also, a harmonized GUV can easily be moved to more remote/unmanned locations and provide independent total ozone column data sets. The GUV instrument in Ny-Ålesund captured well the exceptionally large Arctic ozone depletion in March/April 2020, whereas the GUV instrument in Oslo recorded a mini ozone hole in December 2019 with total ozone values below 200 DU. For all the three Norwegian stations there is a slight increase in total ozone from 1995 until today. Measurements of GUV effective cloud transmittance in Ny-Ålesund indicate that there has been a significant change in albedo during the past 25 years, most likely resulting from increased temperatures and Arctic ice melt in the area surrounding Svalbard.
2021
Eastward-propagating planetary waves prior to the January 2009 sudden stratospheric warming
Eastward-propagating planetary waves (EPWs) were investigated prior to the boreal January 2009 major sudden stratospheric warming (SSW) event simulated by the National Center for Atmospheric Research's Whole Atmosphere Community Climate Model with specified dynamics. About 22 days before SSW onset, a background flow with jet maxima around the upper polar stratosphere and subtropical mesosphere developed due to the net forcing by gravity and planetary waves. The mesospheric wind structure was largely unstable and supported a wave geometry conducive to overreflection. With a zonal phase speed of ∼10 m s−1, EPWs appeared near their turning and critical layers as wavenumber-2 perturbations in the stratosphere and mesosphere. Accompanied by upward EPW activity from the lower stratosphere, EPW growth exhibited characteristics of wave instability and overreflection.
American Geophysical Union (AGU)
2021
The 11 year solar cycle UV irradiance effect and its dependency on the Pacific Decadal Oscillation
The stratospheric, tropospheric and surface impacts from the 11 year ultraviolet solar spectral irradiance (SSI) variability have been extensively studied using climate models and observations. Here, we demonstrate using idealized model simulations that the Pacific Decadal Oscillation (PDO), which has been shown to impact the tropospheric and stratospheric circulation from sub-decadal to multi-decadal timescales, strongly modulates the solar-induced atmospheric response. To this end, we use a high-top version of the coupled ocean–atmosphere Norwegian Climate Prediction Model forced by the SSI dataset recommended for Coupled Model Intercomparison Project 6. We perform a 24-member ensemble experiment over the solar cycle 23 in an idealized framework. To assess the PDO modulation of the solar signal, we divide the model data into the two PDO phases, PDO+ and PDO−, for each solar (maximum or minimum) phase. By compositing and combining the four categories, we hence determine the component of the solar signal that is independent of the PDO and the modulation of the solar signal by the PDO, along with the solar signal in each PDO phase. Reciprocally, we determine the PDO effect in each solar phase. Our results show that the intensification of the polar vortex under solar maximum is much stronger in the PDO− phase. This signal is transferred into the troposphere, where we find a correspondingly stronger polar jet and weaker Aleutian Low. We further show that the amplification of the solar signal by the PDO− phase is driven by anomalous meridional advection of solar-induced temperature anomalies over northern North America and the North Pacific, which contributes to a decreased meridional eddy heat flux and hence to a decreased vertical planetary wave flux into the stratosphere.
2021
A strategy towards the generation of testable adverse outcome pathways for nanomaterials
Manufactured nanomaterials (NMs) are increasingly used in a wide range of industrial applications leading to a constant increase in the market size of nano-enabled products. The increased production and use of NMs are constantly raising concerns among different stakeholder groups with regard to their effects on human and environmental health. Currently, nanosafety hazard assessment is still widely performed using in vivo (animal) models, however the development of robust and regulatory relevant strategies is required to prioritize and/or reduce animal testing. Adverse outcome pathways (AOPs) are a structured representation of biological events that start from a molecular initiating event (MIE) leading to an adverse outcome (AO) through a series of key events (KEs). The AOP framework offers great advancement to risk assessment and regulatory safety assessments. While AOPs for chemicals have been more frequently reported, AOPs collection for NMs is narrow. By using existing AOPs, we aimed to generate simple and testable strategies to predict if a given NM has the potential to induce a MIE leading to an AO through a series of KEs. Firstly, we identified potential MIEs or initial KEs reported for NMs in the literature. Then, we searched the identified MIE or initial KEs as keywords in the AOP-Wiki to find associated AOPs. Finally, using two case studies, we demonstrated here how in vitro strategies can be used for testing the identified MIE/KEs.
Springer
2021
Brominated Flame Retardants in Antarctic Air in the Vicinity of Two All-Year Research Stations
Continuous atmospheric sampling was conducted between 2010–2015 at Casey station in Wilkes Land, Antarctica, and throughout 2013 at Troll Station in Dronning Maud Land, Antarctica. Sample extracts were analyzed for polybrominated diphenyl ethers (PBDEs), and the naturally converted brominated compound, 2,4,6-Tribromoanisole, to explore regional profiles. This represents the first report of seasonal resolution of PBDEs in the Antarctic atmosphere, and we describe conspicuous differences in the ambient atmospheric concentrations of brominated compounds observed between the two stations. Notably, levels of BDE-47 detected at Troll station were higher than those previously detected in the Antarctic or Southern Ocean region, with a maximum concentration of 7800 fg/m3. Elevated levels of penta-formulation PBDE congeners at Troll coincided with local building activities and subsided in the months following completion of activities. The latter provides important information for managers of National Antarctic Programs for preventing the release of persistent, bioaccumulative, and toxic substances in Antarctica.
MDPI
2021