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Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 1: Synthetic dataset for validation of trace gas retrieval algorithms
Get PDFRetrievals of trace gas concentrations from satellite observations are mostly performed for clear regions or regions with low cloud coverage. However, even fully clear pixels can be affected by clouds in the vicinity, either by shadowing or by scattering of radiation from clouds in the clear region. Quantifying the error of retrieved trace gas concentrations due to cloud scattering is a difficult task. One possibility is to generate synthetic data by three-dimensional (3D) radiative transfer simulations using realistic 3D atmospheric input data, including 3D cloud structures. Retrieval algorithms may be applied on the synthetic data, and comparison to the known input trace gas concentrations yields the retrieval error due to cloud scattering. In this paper we present a comprehensive synthetic dataset which has been generated using the Monte Carlo radiative transfer model MYSTIC (Monte Carlo code for the phYSically correct Tracing of photons In Cloudy atmospheres). The dataset includes simulated spectra in two spectral ranges (400–500 nm and the O2A-band from 755–775 nm). Moreover it includes layer air mass factors (layer-AMFs) calculated at 460 nm. All simulations are performed for a fixed background atmosphere for various sun positions, viewing directions and surface albedos. Two cloud setups are considered: the first includes simple box clouds with various geometrical and optical thicknesses. This can be used to systematically investigate the sensitivity of the retrieval error on solar zenith angle, surface albedo and cloud parameters. Corresponding 1D simulations are also provided. The second includes realistic three-dimensional clouds from an ICON large eddy simulation (LES) for a region covering Germany and parts of surrounding countries. The scene includes cloud types typical of central Europe such as shallow cumulus, convective cloud cells, cirrus and stratocumulus. This large dataset can be used to quantify the trace gas concentration retrieval error statistically. Along with the dataset, the impact of horizontal photon transport on reflectance spectra and layer-AMFs is analysed for the box-cloud scenarios. Moreover, the impact of 3D cloud scattering on the NO2 vertical column density (VCD) retrieval is presented for a specific LES case. We find that the retrieval error is largest in cloud shadow regions, where the NO2 VCD is underestimated by more than 20 %. The dataset is available for the scientific community to assess the behaviour of trace gas retrieval algorithms and cloud correction schemes in cloud conditions with 3D structure.publishedVersio
Odds and ends of atmospheric mercury in Europe and over the North Atlantic Ocean: temporal trends of 25 years of measurements
Get PDFThe global monitoring plan of the Minamata Convention on Mercury was established to generate long-term data necessary for evaluating the effectiveness of regulatory measures at a global scale. After 25 years of monitoring (since 1995), Mace Head is one of the atmospheric monitoring stations with the longest mercury record and has produced sufficient data for the analysis of temporal trends of total gaseous mercury (TGM) in Europe and the North Atlantic. Using concentration-weighted trajectories for atmospheric mercury measured at Mace Head as well as another five locations in Europe, Amderma, Andøya, Villum, Waldhof and Zeppelin, we identify the regional probabilistic source contribution factor and its changes for the period of 1996 to 2019. Temporal trends indicate that concentrations of mercury in the atmosphere in Europe and the North Atlantic have declined significantly over the past 25 years at a non-monotonic rate averaging 0.03 . Concentrations of TGM at remote marine sites were shown to be affected by continental long-range transport, and evaluation of reanalysis back trajectories displays a significant decrease in TGM in continental air masses from Europe in the last 2 decades. In addition, using the relationship between mercury and other atmospheric trace gases that could serve as a source signature, we perform factorization regression analysis, based on positive rotatable factorization to solve probabilistic mass functions. We reconstructed atmospheric mercury concentration and assessed the contribution of the major natural and anthropogenic sources. The results reveal that the observed downward trend in the atmospheric mercury is mainly associated with a factor with a high load of long-lived anthropogenic species.publishedVersio
Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 2: Impact on NO2 retrieval and mitigation strategies
Get PDFOperational retrievals of tropospheric trace gases from space-borne spectrometers are based on one-dimensional radiative transfer models. To minimize cloud effects, trace gas retrievals generally implement a simple cloud model based on radiometric cloud fraction estimates and photon path length corrections. The latter relies on measurements of the oxygen collision pair (O2–O2) absorption at 477 nm or on the oxygen A-band around 760 nm to determine an effective cloud height. In reality however, the impact of clouds is much more complex, involving unresolved sub-pixel clouds, scattering of clouds in neighbouring pixels, and cloud shadow effects, such that unresolved three-dimensional effects due to clouds may introduce significant biases in trace gas retrievals. Although clouds have significant effects on trace gas retrievals, the current cloud correction schemes are based on a simple cloud model, and the retrieved cloud parameters must be interpreted as effective values. Consequently, it is difficult to assess the accuracy of the cloud correction only based on analysis of the accuracy of the cloud retrievals, and this study focuses solely on the impact of the 3D cloud structures on the trace gas retrievals. In order to quantify this impact, we study NO2 as a trace gas example and apply standard retrieval methods including approximate cloud corrections to synthetic data generated by the state-of-the-art three-dimensional Monte Carlo radiative transfer model MYSTIC. A sensitivity study is performed for simulations including a box cloud, and the dependency on various parameters is investigated. The most significant bias is found for cloud shadow effects under polluted conditions. Biases depend strongly on cloud shadow fraction, NO2 profile, cloud optical thickness, solar zenith angle, and surface albedo. Several approaches to correct NO2 retrievals under cloud shadow conditions are explored. We find that air mass factors calculated using fitted surface albedo or corrected using the O2–O2 slant column density can partly mitigate cloud shadow effects. However, these approaches are limited to cloud-free pixels affected by surrounding clouds. A parameterization approach is presented based on relationships derived from the sensitivity study. This allows measurements to be identified for which the standard NO2 retrieval produces a significant bias and therefore provides a way to improve the current data flagging approach.publishedVersio
Monitoring of environmental toxics at Franzefoss Eide, Sotra and Husøya, Kristiansund.
Get PDFNILU har gjennomført måleprogram for konsentrasjoner i luft ved Franzefoss Gjenvinning AS sine anlegg ved Eide på Sotra og ved Husøya ved Kristiansund. Ved Eide ble det tatt prøver i luft og analysert for prioriterte miljøgifter som dekloraner, fenoler, ftalater, PFAS, benzotriazoler, organiske tinnforbindelser, samt VOC inkludert D6, ammoniakk (NH3), gassfase HCl og hydrogensulfid (H2S). For de prioriterte miljøgiftene var de fleste prøvene under deteksjonsgrensen. De høyeste verdiene ble observert ved Lokasjon 11 Vannrenseanlegget. Ved Husøya ble det tatt prøver i luft og analysert for VOC inkludert D6, ammoniakk (NH3) og gassfase HCl. Verdiene ved Husøya var lavere enn ved Eide.NILU has conducted a monitoring program for environmental toxics in air at Franzefoss Eide, Sotra (W. Norway) and Husøya, Kristiansund (NW Norway). At Eide, the samples were analyzed for dechlorane, phenols, phthalates, PFAS, benzotriazoles, organotin compounds, as well as VOCs including D6, ammonia (NH3), hydrogen chloride (HCl) and hydrogen sulphide (H2S). At Husøya the samples were analyzed for VOCs including D6, ammonia (NH3) and hydrogen chloride (HCl).publishedVersio
Innhold og migrasjon av tilsetningsstoffer (kjemikalier) fra plastprodukter.
Get PDFNILU has, on behalf of the Norwegian Environment Agency, performed chemical analyses of a selection of additives in plastic products. The goal was to identify content and migration of the chemical additives in and from the products to air and surfaces of the products at room temperature. The plastic products covered extension cord, sockets, flooring, wall papers, upholstery, PC-mouse and PCs. Targeted chemicals were organophosphorous flame retardants (OPFRs), brominated flame retardants (BFRs) including TBBPA, and chlorinated substances. TPHP (triphenyl phosphate) was detected in most sample types, but the highest concentrations were found for TBEP (tris(2-butoxyethyl)phosphate. The highest number of compounds were detected in the PC-mouses and high levels were also found in the surface wipes on PC-mouses. None of the targeted compounds were detected in the air samples.NILU har på oppdrag av Miljødirektoratet utført kjemisk analyse av et utvalg av kjemiske tilsetningsstoffer i plastprodukter. Formålet med studien var å identifisere innhold i og migrasjon av tilsetningsstoffene fra produktene til luft og overflater i romtemperatur. Plastproduktene inkluderte skjøteledninger, stikkontakter, gulv, tapet, møbelstopp, PC-mus og PCer. Kjemisk analyse ble utført for organofosfatflammehemmere, bromerte flammehemmere inklusive TBBPA, og klorerte forbindelser. TPHP (trifenylfosfat) ble detektert i flest prøvetyper, men de høyeste nivåene av innehold ble målt for TBEP (tris(2-butoxyethyl)fosfat. Flest stoffer ble detektert i PC-mus der blant annet halogenerte flammehemmere ble detektert. Høye nivåer i migrasjon til overflater ble også detektert for PC-mus. Ingen av stoffene ble detektert i luftprøver.publishedVersio
Hitting the hotspots – Targeted deployment of air source heat pump technology to deliver clean air communities and climate progress: A case study of Ireland
Get PDFElectrification of residential heating and investment in building energy efficiency are central pillars of many national strategies to reduce carbon emissions from the built environment sector. Ireland has a strong dependence on oil use for central heating and a substantial share of homes still using solid fuels. The current national strategy calls for the retrofitting of 400,000 home heating systems with heat pumps by 2030, principally replacing oil fired heating systems. Displacing natural gas, oil and solid fuel boilers with heat pumps will have a favourable impact on climate outcomes. However, the impact on air pollutant outcomes is far more favourable when solid fuels are replaced, and the positive impact on ambient air quality is much enhanced where concentrated clusters of solid-fuel use are targeted. This research spatially analyses emissions and air pollutant concentration outcomes for both targeted and non-targeted deployments of heat pumps and shows that a focused deployment of just 3% of the national heat pump target on solid-fuel homes could offer similar progress on climate goals but with a substantial impact in terms of reducing air pollution hot spots. For the Irish residential heating season (October–March), the targeted solid fuel scenario delivers average PM2.5 concentration decreases of 20–34%. This paper shows that these targeted communities are often in areas of relative deprivation, and as such, direct support for fabric retrofitting and heat pump technology installation offers the potential to simultaneously advance climate, air and just transition policy ambitions.publishedVersio
Common Considerations for Genotoxicity Assessment of Nanomaterials
Get PDFGenotoxicity testing is performed to determine potential hazard of a chemical or agent for direct or indirect DNA interaction. Testing may be a surrogate for assessment of heritable genetic risk or carcinogenic risk. Testing of nanomaterials (NM) for hazard identification is generally understood to require a departure from normal testing procedures found in international standards and guidelines. A critique of the genotoxicity literature in Elespuru et al., 2018, reinforced evidence of problems with genotoxicity assessment of nanomaterials (NM) noted by many previously. A follow-up to the critique of problems (what is wrong) is a series of methods papers in this journal designed to provide practical information on what is appropriate (right) in the performance of genotoxicity assays altered for NM assessment. In this “Common Considerations” paper, general considerations are addressed, including NM characterization, sample preparation, dosing choice, exposure assessment (uptake) and data analysis that are applicable to any NM genotoxicity assessment. Recommended methods for specific assays are presented in a series of additional papers in this special issue of the journal devoted to toxicology methods for assessment of nanomaterials: the In vitro Micronucleus Assay, TK Mutagenicity assays, and the In vivo Comet Assay. In this context, NM are considered generally as insoluble particles or test articles in the nanometer size range that present difficulties in assessment using techniques described in standards such as OECD guidelines.Common Considerations for Genotoxicity Assessment of NanomaterialspublishedVersio
Decoupling Emission Reductions and Trade-Offs of Policies in Norway Based on a Bottom-Up Traffic Emission Model
Get PDFThe way Norway is spearheading electrification in the transport sector is of global interest. In this study, we used the Norwegian Emissions from Road Vehicle Exhaust (NERVE) model, a bottom-up high-resolution traffic emission model, to calculate all emissions in Norway (2009–2020) and evaluate potential co-benefit and trade-offs of policies to target climate change mitigation, air quality and socioeconomic factors. Results for municipal data with regard to traffic growth, road network influences, vehicle composition, emissions and energy consumption are presented. Light vehicle CO2 emissions per kilometer have been reduced by 22% since 2009, mainly driven by an increasing bio-fuel mixing and battery electric vehicles (BEV) share. BEVs are mostly located in and around the main cities, areas with young vehicle fleets, and strong local incentives. Beneficiaries of BEVs incentives have been a subset of the population with strong economic indicators. The incentivized growth in the share of diesel-fuelled passenger vehicles has been turned, and together with Euro6 emission standards, light vehicle NOx emissions have been halved since peaking in 2014. BEVs represent an investment in emission reductions in years to come, and current sales set Norway up for an accelerated decline in all exhaust emissions despite the continual growth in traffic.publishedVersio
What do we know about the production and release of persistent organic pollutants in the global environment?
No full textInformation on the global production and environmental releases of persistent organic pollutants (POPs) is of critical importance for regulating and eliminating these chemical substances of worldwide environmental and health concerns. Here, we conduct an extensive literature review to collect and curate quantitative information on the historical global production and multimedia environmental releases of 25 intentionally produced POPs. Our assembled data indicate that as of 2020, a cumulative total of 31 306 kilotonnes (kt) of the 25 POPs had been synthesized and commercialized worldwide, resulting in cumulative releases of 20 348 kt into the global environment. As of 2020, short-chain chlorinated paraffins were the most produced POP, with a historical global cumulative tonnage amounting to 8795 kt, whereas α-hexachlorocyclohexane (HCH) had the largest historical global cumulative environmental releases of 6567 kt among these 25 POPs. The 1970s witnessed the peak in the annual global production of the 25 investigated POPs. The United States and Europe used to be the hotspots of environmental releases of the 25 investigated POPs, notably in the 1960s and 1970s. By contrast, global environmental releases occurred primarily in China in the 2000s–2010s. Preliminary efforts are also made to integrate the production volume information with “hazard” attributes (persistence, bioaccumulation, toxicity, and long-range transport potential) in the evaluation of potential environmental impacts of the 25 POPs. The results show that dichlorodiphenyltrichloroethane (DDT) and polychlorinated biphenyls (PCBs) are potentially associated with higher environmental impacts than other POPs because they are among the top rankings in both the global cumulative production and hazard indicators. This work for the first time reveals the astonishing magnitudes of POP production and environmental releases in contemporary human history. It also underscores the importance of tonnage information in assessments of POPs, POP candidates, and other chemicals of emerging concern.publishedVersio