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Calibration and assessment of electrochemical low-cost sensors in remote alpine harsh environments
This work presents results from an original open-source low-cost sensor (LCS) system developed to measure tropospheric O3 in a remote high altitude alpine site. Our study was conducted at the Col Margherita Observatory (2543 m above sea level), in the Italian Eastern Alps. The sensor system mounts three commercial low-cost O3/NO2 sensors that have been calibrated before field deployment against a laboratory standard (Thermo Scientific; 49i-PS), calibrated against the standard reference photometer no. 15 calibration scale of the World Meteorological Organization (WMO). Intra- and intercomparison between the sensors and a reference instrument (Thermo Scientific; 49c) have been conducted for 7 months from May to December 2018. The sensors required an individual calibration, both in laboratory and in the field. The sensor's dependence on the environmental meteorological variables has been considered and discussed. We showed that it is possible to reduce the bias of one LCS by using the average coefficient values of another LCS working in tandem, suggesting a way forward for the development of remote field calibration techniques. We showed that it is possible reconstruct the environmental ozone concentration during the loss of reference instrument data in situations caused by power outages. The evaluation of the analytical performances of this sensing system provides a limit of detection (LOD) <5 ppb (parts per billion), limit of quantification (LOQ) <17 ppb, linear dynamic range (LDR) up to 250 ppb, intra-Pearson correlation coefficient (PCC) up to 0.96, inter-PCC >0.8, bias >3.5 ppb and ±8.5 at 95 % confidence. This first implementation of a LCS system in an alpine remote location demonstrated how to obtain valuable data from a low-cost instrument in a remote environment, opening new perspectives for the adoption of low-cost sensor networks in atmospheric sciences.
2021
2021
2021
2021
Air Quality Plans and Measures. Analysis of data submitted from 2014 to 2020.
The submitted data were analysed with the aim to provide information to the EEA Member countries that can be used to improve their air quality management practices, and to give feedback on data quality and possible use. Previous studies in the framework of the Air Implementation Pilot (published in 2012 and 2013) made assessments of the measures and management practices but were not successful in defining the measures’ effectiveness, so the present report also looks into what kind of information can be obtained from the data.
In the period 2014 – 2020, 23 EEA member countries submitted at least one air quality plan. Most countries focus their plans on pollutants related to traffic: NO2 and/or PM10. Most measures target exceedances of NO2 (62 %), PM10 (26 %) and PM2.5 (10 %), and measures are reported that target exceedances of standards of benzo(a)pyrene, nickel and lead (all in PM10) as well as SO2. In one case, the measure is related to benzene.
« Traffic » is the main sector leading to exceedances, with 64 % of records, followed by « domestic heating » (14 %), « local industry » (10 %) and “Other” (8 %). The « Other » category when given further information could comprise a variety of sources including meteorology, agricultural residue burning, harbour activity or shipping.
The majority of the exceedances occurred in urban areas (65 %) followed by suburban areas (21 %), while 14 % of the exceedances addressed in the plans occurred in rural areas.
The available data consist of a large number of individual records (ranging from several hundreds to over 20 thousand depending on the reporting element) that in theory can be linked using unique identifiers. However, not all the records can be linked. While the basis for analysis can vary depending on which reporting segments are used, the overall results are consistent across the segments, and provide a very good overview of which air pollution abatement measures are taken by national and local authorities.
ETC/ATNI
2021
The Monitoring Nitrous Oxide Sources (MIN2OS) satellite project
The Monitoring Nitrous Oxide Sources (MIN2OS) satellite project aims at monitoring global-scale nitrous oxide (N2O) sources by retrieving N2O surface fluxes from the inversion of space-borne N2O measurements that are sensitive to the lowermost atmospheric layers under favorable conditions. MIN2OS will provide emission estimates of N2O at a horizontal resolution of 1° × 1° on the global scale and 10 × 10 km2 on the regional scale on a weekly to monthly basis depending on the application (e.g., agriculture, national inventories, policy, scientific research). Our novel approach is based on the development of: 1) a space-borne instrument operating in the Thermal InfraRed domain providing, in clear sky conditions, N2O mixing ratio in the lowermost atmosphere (900 hPa) under favorable conditions (summer daytime) over land and under favorable and unfavorable (winter nighttime) conditions over the ocean and 2) an atmospheric inversion framework to estimate N2O surface fluxes from the atmospheric satellite observations. After studying three N2O spectral bands (B1 at 1240–1350 cm−1, B2 at 2150–2260 cm−1 and B3 at 2400–2600 cm−1), a new TIR instrument will be developed, centered at 1250–1330 cm−1, with a resolution of 0.125 cm−1, a Full Width at Half Maximum of 0.25 cm−1 and a swath of 300 km. To optimally constrain the retrieval of N2O vertical profiles, the instrument will be on-board a platform at ~830 km altitude in a sun-synchronous orbit crossing the Equator in descending node at 09:30 local time in synergy with two other platforms (Metop-SG and Sentinel-2 NG) expected to fly in 2031–32 aiming at detecting surface properties, agricultural information on the field scale and vertical profiles of atmospheric constituents and temperature. The lifetime of the MIN2OS project would be 4–5 years to study the interannual variability of N2O surface fluxes. The spectral noise can be decreased by at least a factor of 5 compared to the lowest noise accessible to date with the Infrared Atmospheric Sounding Interferometer-New Generation (IASI-NG) mission. The N2O total error is expected to be less than ~1% (~3 ppbv) along the vertical. The preliminary design of the MIN2OS project results in a small instrument (payload of 90 kg, volume of 1200 × 600 × 300 mm3) with, in addition to the spectrometer, a wide field and 1-km resolution imager for cloud detection. The instruments could be hosted on a small platform, the whole satellite being largely compatible with a dual launch on VEGA-C. The MIN2OS project has been submitted to the European Space Agency Earth Explorer 11 mission ideas.
2021
2021
How Atmospheric Chemistry and Transport Drive Surface Variability of N2O and CFC-11
Nitrous oxide (N2O) is a long-lived greenhouse gas that affects atmospheric chemistry and climate. In this work, we use satellite measurements of N2O, ozone (O3), and temperature from the Aura Microwave Limb Sounder (MLS) instrument to calculate stratospheric loss of N2O, and thus its atmospheric lifetime. Using three chemistry transport models simulating the Aura period 2005–2017, we verify the stratospheric sink using MLS data and follow that loss signal down to the surface and compare with surface observations. Stratospheric loss has a strong seasonal cycle and is further modulated by the Quasi-Biennial Oscillation (QBO); these cycles are seen equally in both observations and the models. When filtered for interannual variability, the modeled surface signal is QBO-caused, and it reproduces the observed pattern, highlighting the potential role of the QBO in tropospheric chemistry and composition, as well as in model evaluation. The observed annual surface signal in the northern hemisphere matches well with the models run without emissions, indicating the annual cycle is driven mostly by stratosphere-troposphere exchange (STE) flux of N2O-depleted air and not surface N2O emissions. In the southern hemisphere (SH), all three models disagree and thus provide no guidance, except for indicating that modeling annual STE in the SH remains a major model uncertainty. Parallel model simulations of CFCl3, which has greater stratospheric loss that N2O and possibly surreptitious emissions, show that its interannual variations parallel those of N2O, and thus the observed N2O variability can identify the stratospheric component of the observed CFCl3 variability.
2021
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.
2021
2021
2021
Impacts of Short-lived Climate Forcers on Arctic Climate, Air Quality, and Human Health
Arctic Monitoring and Assessment Programme (AMAP)
2021
This program, «Monitoring of environmental contaminants in freshwater ecosystems and single species in large Norwegian lakes”, has covered sampling and determination of environmental contaminants by analyses of organisms in an aquatic, pelagic food web of Lake Mjøsa, and in the top predator in Lake Femunden. Samples of different trophic levels, from epipelagic zooplankton to the top predator brown trout, were collected during the late stages of the growth season in 2020. In this report, the status of contamination in the food web, trends and biomagnification potential of various environmental contaminants is discussed.
Norsk institutt for vannforskning (NIVA)
2021
Dimethyl Sulfide-Induced Increase in Cloud Condensation Nuclei in the Arctic Atmosphere
Oceanic dimethyl sulfide (DMS) emissions have been recognized as a biological regulator of climate by contributing to cloud formation. Despite decades of research, the climatic role of DMS remains ambiguous largely because of limited observational evidence for DMS-induced cloud condensation nuclei (CCN) enhancement. Here, we report concurrent measurement of DMS, physiochemical properties of aerosol particles, and CCN in the Arctic atmosphere during the phytoplankton bloom period of 2010. We encountered multiple episodes of new particle formation (NPF) and particle growth when DMS mixing ratios were both low and high. The growth of particles to sizes at which they can act as CCN accelerated in response to an increase in atmospheric DMS. Explicitly, the sequential increase in all relevant parameters (including the source rate of condensable vapor, the growth rate of particles, Aitken mode particles, hygroscopicity, and CCN) was pronounced at the DMS-derived NPF and particle growth events. This field study unequivocally demonstrates the previously unconfirmed roles of DMS in the growth of particles into climate-relevant size and eventual CCN activation.
2021
A comprehensive European dataset on monthly atmospheric NH3, acid gases (HNO3, SO2, HCl), and aerosols (NH+4, NO−3, SO2−4, Cl−, Na+, Ca2+, Mg2+) is presented and analysed. Speciated measurements were made with a low-volume denuder and filter pack method (DEnuder for Long-Term Atmospheric sampling, DELTA®) as part of the EU NitroEurope (NEU) integrated project. Altogether, there were 64 sites in 20 countries (2006–2010), coordinated between seven European laboratories. Bulk wet-deposition measurements were carried out at 16 co-located sites (2008–2010). Inter-comparisons of chemical analysis and DELTA® measurements allowed an assessment of comparability between laboratories.
The form and concentrations of the different gas and aerosol components measured varied between individual sites and grouped sites according to country, European regions, and four main ecosystem types (crops, grassland, forests, and semi-natural). The smallest concentrations (with the exception of SO2−4 and Na+) were in northern Europe (Scandinavia), with broad elevations of all components across other regions. SO2 concentrations were highest in central and eastern Europe, with larger SO2 emissions, but particulate SO2−4 concentrations were more homogeneous between regions. Gas-phase NH3 was the most abundant single measured component at the majority of sites, with the largest variability in concentrations across the network. The largest concentrations of NH3, NH+4, and NO−3 were at cropland sites in intensively managed agricultural areas (e.g. Borgo Cioffi in Italy), and the smallest were at remote semi-natural and forest sites (e.g. Lompolojänkkä, Finland), highlighting the potential for NH3 to drive the formation of both NH+4 and NO−3 aerosol. In the aerosol phase, NH+4 was highly correlated with both NO−3 and SO2−4, with a near-1:1 relationship between the equivalent concentrations of NH+4 and sum (NO−3+ SO2−4),of which around 60 % was as NH4NO3.
Distinct seasonality was also observed in the data, influenced by changes in emissions, chemical interactions, and the influence of meteorology on partitioning between the main inorganic gases and aerosol species. Springtime maxima in NH3 were attributed to the main period of manure spreading, while the peak in summer and trough in winter were linked to the influence of temperature and rainfall on emissions, deposition, and gas–aerosol-phase equilibrium. Seasonality in SO2 was mainly driven by emissions (combustion), with concentrations peaking in winter, except in southern Europe, where the peak occurred in summer. Particulate SO2−4 showed large peaks in concentrations in summer in southern and eastern Europe, contrasting with much smaller peaks occurring in early spring in other regions. The peaks in particulate SO2−4 coincided with peaks in NH3 concentrations, attributed to the formation of the stable (NH4)2SO4. HNO3 concentrations were more complex, related to traffic and industrial emissions, photochemistry, and HNO3:NH4NO3 partitioning. While HNO3 concentrations were seen to peak in the summer in eastern and southern Europe (increased photochemistry), the absence of a spring peak in HNO3 in all regions may be explained by the depletion of HNO3 through reaction with surplus NH3 to form the semi-volatile aerosol NH4NO3. Cooler, wetter conditions in early spring favour the formation and persistence of NH4NO3 in the aerosol phase, consistent with the higher springtime concentrations of NH+4 and NO−3. The seasonal profile of NO−3 was mirrored by NH+4, illustrating the influence of gas–aerosol partitioning of NH4NO3 in the seasonality of these components.
Gas-phase NH3 and aerosol NH4NO3 were the dominant species in the total inorganic gas and aerosol species measured in the NEU network. With the current and projected trends in SO2, NOx, and NH3 emissions, concentrations of NH3 and NH4NO3 can be expected to continue to dominate...
2021
Hemispheric black carbon increase after the 13th-century Māori arrival in New Zealand
New Zealand was among the last habitable places on earth to be colonized by humans. Charcoal records indicate that wildfires were rare prior to colonization and widespread following the 13th- to 14th-century Māori settlement, but the precise timing and magnitude of associated biomass-burning emissions are unknown, as are effects on light-absorbing black carbon aerosol concentrations over the pristine Southern Ocean and Antarctica. Here we used an array of well-dated Antarctic ice-core records to show that while black carbon deposition rates were stable over continental Antarctica during the past two millennia, they were approximately threefold higher over the northern Antarctic Peninsula during the past 700 years. Aerosol modelling demonstrates that the observed deposition could result only from increased emissions poleward of 40° S—implicating fires in Tasmania, New Zealand and Patagonia—but only New Zealand palaeofire records indicate coincident increases. Rapid deposition increases started in 1297 (±30 s.d.) in the northern Antarctic Peninsula, consistent with the late 13th-century Māori settlement and New Zealand black carbon emissions of 36 (±21 2 s.d.) Gg y−1 during peak deposition in the 16th century. While charcoal and pollen records suggest earlier, climate-modulated burning in Tasmania and southern Patagonia, deposition in Antarctica shows that black carbon emissions from burning in New Zealand dwarfed other preindustrial emissions in these regions during the past 2,000 years, providing clear evidence of large-scale environmental effects associated with early human activities across the remote Southern Hemisphere.
2021
2021
2021
2021
Global environment outlook - Geo-6. Technical summary
he sixth Global Environment Outlook was launched in 2019 at the fourth UN Environment Assembly. It highlighted the ongoing damage to life and health from pollution and land degradation, and warned that zoonosis was already accounting for more than 60% of human infectious diseases. Since then the spread of COVID-19 has demonstrated the enormous challenges a global pandemic can cause for health care systems and the economy, as well as revealing potential environmental benefits of an altered lifestyle. This Technical Summary synthesizes the science and data in the GEO-6 report to make it accessible to a broad audience of policymakers, students and scientists. It demonstrates that more urgent and sustained action is required to address the degradation caused by our energy, food and waste systems and identifies a variety of transformational pathways for those seeking far-reaching policies for environmental and economic recovery.
Cambridge University Press
2021