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Seasonality of aerosol optical properties in the Arctic
Given the sensitivity of the Arctic climate to short-lived climate forcers, long-term in situ surface measurements of aerosol parameters are useful in gaining insight into the magnitude and variability of these climate forcings. Seasonality of aerosol optical properties – including the aerosol light-scattering coefficient, absorption coefficient, single-scattering albedo, scattering Ångström exponent, and asymmetry parameter – are presented for six monitoring sites throughout the Arctic: Alert, Canada; Barrow, USA; Pallas, Finland; Summit, Greenland; Tiksi, Russia; and Zeppelin Mountain, Ny-Ålesund, Svalbard, Norway. Results show annual variability in all parameters, though the seasonality of each aerosol optical property varies from site to site. There is a large diversity in magnitude and variability of scattering coefficient at all sites, reflecting differences in aerosol source, transport, and removal at different locations throughout the Arctic. Of the Arctic sites, the highest annual mean scattering coefficient is measured at Tiksi (12.47Mm−1), and the lowest annual mean scattering coefficient is measured at Summit (1.74Mm−1). At most sites, aerosol absorption peaks in the winter and spring, and has a minimum throughout the Arctic in the summer, indicative of the Arctic haze phenomenon; however, nuanced variations in seasonalities suggest that this phenomenon is not identically observed in all regions of the Arctic. The highest annual mean absorption coefficient is measured at Pallas (0.48Mm−1), and Summit has the lowest annual mean absorption coefficient (0.12Mm−1). At the Arctic monitoring stations analyzed here, mean annual single-scattering albedo ranges from 0.909 (at Pallas) to 0.960 (at Barrow), the mean annual scattering Ångström exponent ranges from 1.04 (at Barrow) to 1.80 (at Summit), and the mean asymmetry parameter ranges from 0.57 (at Alert) to 0.75 (at Summit). Systematic variability of aerosol optical properties in the Arctic supports the notion that the sites presented here measure a variety of aerosol populations, which also experience different removal mechanisms. A robust conclusion from the seasonal cycles presented is that the Arctic cannot be treated as one common and uniform environment but rather is a region with ample spatiotemporal variability in aerosols. This notion is important in considering the design or aerosol monitoring networks in the region and is important for informing climate models to better represent short-lived aerosol climate forcers in order to yield more accurate climate predictions for the Arctic.
2018
2009
2011
2016
Seasonal Variation of Wet Deposition of Black Carbon at Ny-Ålesund, Svalbard
American Geophysical Union (AGU)
2021
2016
2011
2015
2018
2000
Field data from two latitudinal transects in Europe and Canada were gathered to better characterize the atmospheric fate of three cyclic methylsiloxanes (cVMSs), i.e., octamethyl-cyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6). During a year-long, seasonally resolved outdoor air sampling campaign, passive samplers with an ultra-clean sorbent were deployed at 15 sampling sites covering latitudes ranging from the source regions (43.7–50.7 °N) to the Arctic (79–82.5 °N). For each site, one of two passive samplers and one of two field blanks were separately extracted and analyzed for the cVMSs at two different laboratories using gas-chromatography-mass spectrometry. Whereas the use of a particular batch of sorbent and the applied cleaning procedure to a large extent controlled the levels of cVMS in field blanks, and therefore also the method detection and quantification limits, minor site-specific differences in field blank contamination were apparent. Excellent agreement between duplicates was obtained, with 95% of the concentrations reported by the two laboratories falling within a factor of 1.6 of each other. Nearly all data show a monotonic relationship between the concentration and distance from the major source regions. Concentrations in source regions were comparatively constant throughout the year, while the concentration gradient towards remote regions became steeper during summer when removal via OH radicals is at its maximum. Concentrations of the different cVMS oligomers were highly correlated within a given transect. Changes in relative abundance of cVMS oligomers along the transect were in agreement with relative atmospheric degradation rates via OH radicals.
Royal Society of Chemistry (RSC)
2023
2016
2010
Plastic pollution is a global and increasing threat to ecosystems. Plastics in the oceans are unevenly distributed, are transported by currents and can now be found in the most remote environments, including Arctic sea ice. The entanglement of wildlife by large plastic debris such as ropes is an obvious and well documented threat. However, the risks associated with the ingestion of smaller plastic particles, including microplastics (< 5mm) have been largely overlooked. Recent studies show that microplastic accumulates in the food web. Even in the Arctic and the deep sea, fish frequently contain microplastics in their guts. This, together with the fact that small microplastic particles can pass from the gut into blood and organs and also leach associated toxic additives raises health concerns for wildlife that ingest microplastic.
Within the North Atlantic, plastic ingestion in seabirds has been studied systematically only in the northern fulmar (Fulmarus glacialis), for which plastic particles > 1mm found in the stomachs of dead (beached or bycaught) birds are quantified. With the origin of these birds being unknown, it is, however, impossible to assess how plastics affect populations even of this one monitored species, let alone for other seabird species that differ in their foraging behaviour and risk to ingest plastics.
This report sums up the results of a workshop which aimed to identify possibilities for long-term monitoring of (micro-) plastic ingestion by seabirds in the framework of SEAPOP, the basal programme monitoring the performance of Norwegian seabird populations (www.seapop.no). The key conclusions were: 1) There is a need for baseline information on plastic ingestion across all seabird species to identify which species and populations are most suitable for monitoring. To obtain this information, the best approach is to investigate the stomach contents of dead birds (i.e. comparable methodology across all species). For long-term monitoring, not only species with high plastic ingestion are of interest, but also those with low plastic prevalence. 2) In the absence of information from (1), eight species that are complementary in their foraging behaviour and have a wide distribution range were selected as preliminary species of interest to monitor plastic ingestion. 3) For minimally invasive monitoring, regurgitates, fresh prey items and faeces are most suitable; 4) More information on prevalence of plastic ingestion is needed to identify optimal sample sizes for long-term monitoring. We therefore highlight the need for several pilot studies before establishing a plastic monitoring protocol within SEAPOP.
Norsk institutt for naturforskning (NINA)
2019
2004
2019
2007
2002
The effective enrichment of perfluoroalkyl acids (PFAAs) in sea spray aerosols (SSA) demonstrated in previous laboratory studies suggests that SSA is a potential source of PFAAs to the atmosphere. In order to investigate the influence of SSA on atmospheric PFAAs in the field, 48 h aerosol samples were collected regularly between 2018 and 2020 at two Norwegian coastal locations, Andøya and Birkenes. Significant correlations (p < 0.05) between the SSA tracer ion, Na+, and PFAA concentrations were observed in the samples from both locations, with Pearson’s correlation coefficients (r) between 0.4–0.8. Such significant correlations indicate SSA to be an important source of atmospheric PFAAs to coastal areas. The correlations in the samples from Andøya were observed for more PFAA species and were generally stronger than in the samples from Birkenes, which is located further away from the coast and closer to urban areas than Andøya. Factors such as the origin of the SSA, the distance of the sampling site to open water, and the presence of other PFAA sources (e.g., volatile precursor compounds) can have influence on the contribution of SSA to PFAA in air at the sampling sites and therefore affect the observed correlations between PFAAs and Na+.
2021
2023
2005
Screening Programme 2022. New environmental pollutants.
Norsk institutt for vannforskning
2023