| 1. |
- Boy, M., et al.
(författare)
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Interactions between the atmosphere, cryosphere, and ecosystems at northern high latitudes
- 2019
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Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 19:3, s. 2015-2061
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Tidskriftsartikel (refereegranskat)abstract
- The Nordic Centre of Excellence CRAICC (Cryosphere-Atmosphere Interactions in a Changing Arctic Climate), funded by NordForsk in the years 2011-2016, is the largest joint Nordic research and innovation initiative to date, aiming to strengthen research and innovation regarding climate change issues in the Nordic region. CRAICC gathered more than 100 scientists from all Nordic countries in a virtual centre with the objectives of identifying and quantifying the major processes controlling Arctic warming and related feedback mechanisms, outlining strategies to mitigate Arctic warming, and developing Nordic Earth system modelling with a focus on short-lived climate forcers (SLCFs), including natural and anthropogenic aerosols. The outcome of CRAICC is reflected in more than 150 peer-reviewed scientific publications, most of which are in the CRAICC special issue of the journal Atmospheric Chemistry and Physics. This paper presents an overview of the main scientific topics investigated in the centre and provides the reader with a state-of-the-art comprehensive summary of what has been achieved in CRAICC with links to the particular publications for further detail. Faced with a vast amount of scientific discovery, we do not claim to completely summarize the results from CRAICC within this paper, but rather concentrate here on the main results which are related to feedback loops in climate change-cryosphere interactions that affect Arctic amplification.
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| 2. |
- Fowler, D., et al.
(författare)
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Atmospheric composition change : Ecosystems-Atmosphere interactions
- 2009
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 43:33, s. 5193-5267
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Forskningsöversikt (refereegranskat)abstract
- Ecosystems and the atmosphere: This review describes the state of understanding the processes involved in the exchange of trace gases and aerosols between the earth's surface and the atmosphere. The gases covered include NO, NO2, HONO, HNO3, NH3, SO2, DMS, Biogenic VOC, O-3, CH4, N2O and particles in the size range 1 nm-10 mu m including organic and inorganic chemical species. The main focus of the review is on the exchange between terrestrial ecosystems, both managed and natural and the atmosphere, although some new developments in ocean-atmosphere exchange are included. The material presented is biased towards the last decade, but includes earlier work, where more recent developments are limited or absent. New methodologies and instrumentation have enabled, if not driven technical advances in measurement. These developments have advanced the process understanding and upscaling of fluxes, especially for particles, VOC and NH3. Examples of these applications include mass spectrometric methods, such as Aerosol Mass Spectrometry (AMS) adapted for field measurement of atmosphere-surface fluxes using micrometeorological methods for chemically resolved aerosols. Also briefly described are some advances in theory and techniques in micrometeorology. For some of the compounds there have been paradigm shifts in approach and application of both techniques and assessment. These include flux measurements over marine surfaces and urban areas using micrometeorological methods and the up-scaling of flux measurements using aircraft and satellite remote sensing. The application of a flux-based approach in assessment of O-3 effects on vegetation at regional scales is an important policy linked development secured through improved quantification of fluxes. The coupling of monitoring, modelling and intensive flux measurement at a continental scale within the NitroEurope network represents a quantum development in the application of research teams to address the underpinning science of reactive nitrogen in the cycling between ecosystems and the atmosphere in Europe. Some important developments of the science have been applied to assist in addressing policy questions, which have been the main driver of the research agenda, while other developments in understanding have not been applied to their wider field especially in chemistry-transport models through deficiencies in obtaining appropriate data to enable application or inertia within the modelling community. The paper identifies applications, gaps and research questions that have remained intractable at least since 2000 within the specialized sections of the paper, and where possible these have been focussed on research questions for the coming decade.
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| 3. |
- Merkulova, Lena, et al.
(författare)
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Effect of Wind Speed on Moderate Resolution Imaging Spectroradiometer (MODIS) Aerosol Optical Depth over the North Pacific
- 2018
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Ingår i: Atmosphere. - : MDPI AG. - 2073-4433 .- 2073-4433. ; 9:2
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Tidskriftsartikel (refereegranskat)abstract
- The surface-wind speed influences on aerosol optical depth (AOD), derived from the Moderate Resolution Imaging Spectroradiometer (MODIS) Aqua daily observations over the central North Pacific during the period 2003-2016, have been investigated in this study. The cloud coverage is relatively low over the present investigation area compared to other marine areas, which favors AOD derived from passive remote sensing from space. In this study, we have combined MODIS AOD with 2 m wind speed (U-2m) on a satellite-pixel basis, which has been interpolated from National Centers for Environmental Prediction (NCEP) reanalysis. In addition, daily averaged AOD derived from Aerosol Robotic Network (AERONET) measurements in the free-troposphere at the Mauna Loa Observatory (3397 m above sea level), Hawaii, was subtracted from the MODIS column AOD values. The latter was to reduce the contribution of aerosols above the planetary boundary layer. This study shows relatively strong power-law relationships between MODIS mean AOD and surface-wind speed for marine background conditions in summer, fall and winter of the current period. However, previous established relationships between AOD and surface-wind speed deviate substantially. Even so, for similar marine conditions the present relationship agrees reasonable well with a power-law relationship derived for north-east Atlantic conditions. The present MODIS retrievals of AOD in the marine atmosphere agree reasonably well with ground-based remote sensing of AOD.
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| 4. |
- Nilsson, Ernst Douglas, et al.
(författare)
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Baltic Sea Spray Emissions : In Situ Eddy Covariance Fluxes vs. Simulated Tank Sea Spray
- 2021
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Ingår i: Atmosphere. - : MDPI AG. - 2073-4433 .- 2073-4433. ; 12:2
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Tidskriftsartikel (refereegranskat)abstract
- We present the first ever evaluation of sea spray aerosol eddy covariance (EC) fluxes at near coastal conditions and with limited fetch, and the first over water with brackish water (on average 7 ppt). The measurements were made on the island of Garpen in the Baltic Sea (56°23′ N, 16°06′ E) in September 2005. We found that wind speed is a major factor that is driving an exponential increase in sea spray sea salt emissions, comparable to previous studies over waters with higher salinity. We were able to show that the inclusion of a thermodenuder in the EC system allowed for the parallel measurements of the dry unheated aerosol flux (representing both organic and sea salt sea spray emissions) and the heated (300 °C) non-volatile sea salt emissions. This study’s experimental approach also included measurements of the artificial sea spray formed in a tank in locally sampled water at the same location as the EC fluxes. We attempted to use the EC aerosol flux measurements to scale the tank measurements to aerosol emissions in order to derive a complete size distribution for the sea spray emission fluxes below the size range (0.3–2 µm dry diameter) of the optical particle counters (OPCs) in the EC system, covering in total 0.01 µm to 2 µm diameter. In the wind directions with long fetches (corresponding to conditions similar to open sea), we were able to distinguish between the aerosol emission fluxes of dry aerosol and heated non-volatile (sea salt only) in the smallest size bins of the OPC, and could therefore indirectly estimate the organic sea spray fraction. In agreement with several previous ambient and tank experiments deriving the size resolved chemical mass concentration of sea salt and water-insoluble organic sea spray, our EC fluxes showed that sea sprays were dominated by sea salt at sizes ≥1 µm diameter, and by organics at the smallest OPC sizes. Since we used direct measures of the sea spray emission fluxes, we confirmed previous suggestions that this size distribution of sea salt and organics is a signature of sea spray aerosols. We were able to show that two sea salt source parameterizations (Mårtensson et al. (2003) and Salter et al. (2015)) agreed fairly well with our observed heated EC aerosol emission fluxes, as long as their predicted emissions were modified for the actual salinity by shifting the particle diameters proportionally to the cubic rote of the salinity. If, in addition, we added organics to the parameterized sea spray following the mono-layer model by Ellison et al. (1999), the combined sea spray parameterizations for sea salt and organics fell reasonably close to the observed fluxes for diameters > 0.15 µm, while one of them overpredicted the sea spray emissions below this size. The organic mono-layer model by Ellison et al. appeared to be able to explain most of the differences we observed between the aerosol emission fluxes with and without the thermodenuder.
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| 5. |
- Rosati, Bernadette, et al.
(författare)
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The impact of atmospheric oxidation on hygroscopicity and cloud droplet activation of inorganic sea spray aerosol
- 2021
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Sea spray aerosol (SSA) contributes significantly to natural aerosol particle concentrations globally, in marine areas even dominantly. The potential changes of the omnipresent inorganic fraction of SSA due to atmospheric ageing is largely unexplored. In the atmosphere, SSA may exist as aqueous phase solution droplets or as dried solid or amorphous particles. We demonstrate that ageing of liquid NaCl and artificial sea salt aerosol by exposure to ozone and UV light leads to a substantial decrease in hygroscopicity and cloud activation potential of the dried particles of the same size. The results point towards surface reactions on the liquid aerosols that are more crucial for small particles and the formation of salt structures with water bound within the dried aerosols, termed hydrates. Our findings suggest an increased formation of hydrate forming salts during ageing and the presence of hydrates in dried SSA. Field observations indicate a reduced hygroscopic growth factor of sub-micrometre SSA in the marine atmosphere compared to fresh laboratory generated NaCl or sea salt of the same dry size, which is typically attributed to organic matter or sulphates. Aged inorganic sea salt offers an additional explanation for such a measured reduced hygroscopic growth factor and cloud activation potential.
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| 6. |
- Zinke, Julika, 1995-
(författare)
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Factors influencing emission fluxes and bacterial enrichment in sea spray aerosols : Insights from laboratory and field studies
- 2023
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Sea spray aerosol (SSA) is one of the major natural aerosol sources and is produced when wave breaking entrains air into ocean surface water, which subsequently breaks up into bubbles. These bubbles rise to the surface and can scavenge biogenic material. Once they reach the surface, they burst and produce both a large number of relatively small film drops that result from the disintegration of the bubble film cap and a smaller number of jet drops that result from the collapse of the bubble cavity and are typically larger in size than the film drops. The production of SSA is influenced by several factors, including wind speed, sea state, seawater temperature, salinity, and the physicochemical and biological condition of the ocean. SSA can significantly impact Earth's radiation budget by scattering incoming solar radiation directly and by acting as cloud condensation nuclei. To improve our understanding of the impact of sea spray aerosols on the Earth’s climate, it is critical to understand the physical mechanisms which determine the size-resolved SSA production flux. Furthermore, SSA can be a vector for the emission of primary biological airborne particles (PBAP) from the oceans to the atmosphere. PBAP encompass bacteria, viruses, pollen and spores and can be present in the atmosphere in form of agglomerates, single particles or cell fractions. Although, the abundance of PBAP typically only make up < 0.1% of the number of aerosols, this does not imply their insignificance. On the contrary, PBAP are known to be very efficient cloud- and ice condensation nuclei and thus can influence cloud properties such as cloud phase, albedo and lifetime, thereby affecting the Earth’s climate as well as biogeochemical cycles. As the Earth is 70% covered by oceans, of which most could be characterized as remote, quantifying the PBAP emissions over these waters are important for the enhancement of climate models.The goal of this thesis was to study the factors impacting SSA emissions and the emission of primary biological particles with SSA with particular focus on bacteria emissions. This was done both through laboratory and field experiments in the Baltic Sea and in the Azores archipelago using a plunging jet sea spray simulation chamber and various techniques to characterize aerosol emissions. More specifically, a parameterization for the SSA production flux as a function of salinity and temperature was derived from laboratory experiments and a wind speed and sea state dependent parameterization were derived from ambient eddy covariance (EC) flux measurements in the Baltic Sea. The combination of EC flux measurements and laboratory generated SSA allowed to derive a chamber specific scaling factor that could be applied to derive bacteria emission fluxes ranging between 16-63 cells m−2 s−1 from the Baltic Sea. Bacteria were found to be 13-488 and 9-148 times enriched in SSA compared to the underlying seawater from mesocosm experiments in the Baltic Sea and Azores, respectively. A comparison of single cell abundance estimates from fluorescence microscopy and real-time measurements of PBAP with diameters > 0.8 µm using a bioaerosol sensor revealed that the latter yielded consistently lower concentrations. The discrepancy was explained by differences in the sampling approach and size cut-offs (i.e. single cells versus agglomerates or particle-attached cells). As such, both methods are applicable to different research questions and should be considered complementary.An analysis of the microbial community composition in the aerosols and underlying seawater showed selective aerosolization of certain bacteria taxa. Furthermore, selective growth and a decrease in alpha diversity in the seawater was observed when the mesocosm experiments were operated in a closed mode (meaning that the seawater was not exchanged over the duration of each experiment), which can however be circumvented by continuously replacing the water in the mesocosm.Ambient measurements of PBAP revealed diurnal variations with a peak during the early morning hours that was correlated to changes wind speed, wave height, air temperature, relative humidity, latent and sensitive heat flux.
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| 7. |
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| 8. |
- Rutgersson, Anna, 1971-, et al.
(författare)
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Using land-based stations for air–sea interaction studies
- 2020
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Ingår i: Tellus. Series A, Dynamic meteorology and oceanography. - : Informa UK Limited. - 0280-6495 .- 1600-0870. ; 72:1, s. 1-23
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Tidskriftsartikel (refereegranskat)abstract
- In situ measurements representing the marine atmosphere and air-sea interaction are taken at ships, buoys, stationary moorings and land-based towers, where each observation platform has structural restrictions. Air-sea fluxes are often small, and due to the limitations of the sensors, several corrections are applied. Land-based towers are convenient for long-term observations, but one critical aspect is the representativeness of marine conditions. Hence, a careful analysis of the sites and the data is necessary. Based on the concept of flux footprint, we suggest defining flux data from land-based marine micrometeorological sites in categories depending on the type of land influence:1. CAT1: Marine data representing open sea,2. CAT2: Disturbed wave field resulting in physical properties different from open sea conditions and heterogeneity of water properties in the footprint region, and3. CAT3: Mixed land-sea footprint, very heterogeneous conditions and possible active carbon production/consumption.Characterization of data would be beneficial for combined analyses using several sites in coastal and marginal seas and evaluation/comparison of properties and dynamics. Aerosol fluxes are a useful contribution to characterizing a marine micrometeorological field station; for most conditions, they change sign between land and sea sectors. Measured fluxes from the land-based marine station Ostergarnsholm are used as an example of a land-based marine site to evaluate the categories and to present an example of differences between open sea and coastal conditions. At the Ostergarnsholm site the surface drag is larger for CAT2 and CAT3 than for CAT1 when wind speed is below 10m/s. The heat and humidity fluxes show a distinctive distinguished seasonal cycle; latent heat flux is larger for CAT2 and CAT3 compared to CAT1. The flux of carbon dioxide is large from the coastal and land-sea sectors, showing a large seasonal cycle and significant variability (compared to the open sea sector). Aerosol fluxes are partly dominated by sea spray emissions comparable to those observed at other open sea conditions.
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| 9. |
- Ahlm, Lars, 1976-, et al.
(författare)
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A comparison of dry and wet season aerosol number fluxes over the Amazon rain forest
- 2010
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 10:6, s. 3063-3079
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Tidskriftsartikel (refereegranskat)abstract
- Vertical number fluxes of aerosol particles and vertical fluxes of CO2 were measured with the eddy covariance method at the top of a 53m high tower in the Amazon rain forest as part of the LBA (The Large Scale Biosphere Atmosphere Experiment in Amazonia) experiment. The observed aerosol number fluxes included particles with sizes down to 10 nm in diameter. The measurements were carried out during the wet and dry season in 2008. In this study focus is on the dry season aerosol fluxes, with significant influence from biomass burning, and these are compared with aerosol fluxes measured during the wet season. Net particle deposition fluxes dominated in daytime in both seasons and the deposition flux was considerably larger in the dry season due to the much higher dry season particle concentration. The particle transfer velocity increased linearly with increasing friction velocity in both seasons. The difference in transfer velocity between the two seasons was small, indicating that the seasonal change in aerosol number size distribution is not enough for causing any significant change in deposition velocity. In general, particle transfer velocities in this study are low compared to studies over boreal forests. The reasons are probably the high percentage of accumulation mode particles and the low percentage of nucleation mode particles in the Amazon boundary layer, both in the dry and wet season, and low wind speeds in the tropics compared to the midlatitudes. In the dry season, nocturnal particle fluxes behaved very similar to the nocturnal CO2 fluxes. Throughout the night, the measured particle flux at the top of the tower was close to zero, but early in the morning there was an upward particle flux peak that is not likely a result of entrainment or local pollution. It is possible that these morning upward particle fluxes are associated with emission of primary biogenic particles from the rain forest. Emitted particles may be stored within the canopy during stable conditions at nighttime, similarly to CO2, and being released from the canopy when conditions become more turbulent in the morning.
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| 10. |
- Ahlm, Lars, et al.
(författare)
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Emission and dry deposition of accumulation mode particles in the Amazon Basin
- 2010
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 10:21, s. 10237-10253
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Tidskriftsartikel (refereegranskat)abstract
- Size-resolved vertical aerosol number fluxes of particles in the diameter range 0.25–2.5 μm were measured with the eddy covariance method from a 53 m high tower over the Amazon rain forest, 60 km NNW of Manaus, Brazil. This study focuses on data measured during the relatively clean wet season, but a shorter measurement period from the more polluted dry season is used as a comparison. Size-resolved net particle fluxes of the five lowest size bins, representing 0.25–0.45 μm in diameter, pointed downward in more or less all wind sectors in the wet season. This is an indication that the source of primary biogenic aerosol particles may be small in this particle size range. In the diameter range 0.5–2.5 μm, vertical particle fluxes were highly dependent on wind direction. In wind sectors where anthropogenic influence was low, net emission fluxes dominated. However, in wind sectors associated with higher anthropogenic influence, net deposition fluxes dominated. The net emission fluxes were interpreted as primary biogenic aerosol emission, but deposition of anthropogenic particles seems to have masked this emission in wind sectors with higher anthropogenic influence. The emission fluxes were at maximum in the afternoon when the mixed layer is well developed, and these emissions were best correlated with horizontal wind speed by the equation log10F=0.47·U+2.26 where F is the emission number flux of 0.5–2.5 μm particles [m−2s−1] and U is the horizontal wind speed [ms−1] at the top of the tower.
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