| 1. |
- Aamaas, Borgar, et al.
(författare)
-
Elemental carbon deposition to Svalbard snow from Norwegian settlements and long-range transport
- 2011
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 63:3, s. 340-351
-
Tidskriftsartikel (refereegranskat)abstract
- The impact on snow pack albedo from local elemental carbon (EC) sources in Svalbard has been investigated for the winter of 2008. Highly elevated EC concentrations in the snow are observed around the settlements of Longyearbyen and Svea (locally > 1000 ng g(-1), about 200 times over the background level), while EC concentrations similar to the background level are seen around Ny-Alesund. Near Longyearbyen and Svea, darkened snow influenced by wind transported coal dust from open coal stockpiles is clearly visible from satellite images and by eye at the ground. As a first estimate, the reduction in snow albedo caused by local EC pollution from the Norwegian settlements has been compared to the estimated reduction caused by long-range transported EC for entire Svalbard. The effect of local EC from Longyearbyen, Svea and all Norwegian settlements are estimated to 2.1%, 7.9% and 10% of the total impact of EC, respectively. The EC particles tend to stay on the surface during melting, and elevated EC concentrations due to the spring melt was observed. This accumulation of EC enhances the positive albedo feedbacks. The EC concentrations were observed to be larger in metamorphosed snow than in fresh snow, and especially around ice lenses.
|
|
| 2. |
- Andersson, Camilla, 1979-, et al.
(författare)
-
Interannual variation and trends in air pollution over Europe due to climate variability during 1958–2001 simulated with a regional CTM coupled to the ERA40 reanalysis
- 2007
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - Stockholm : Tellus. - 0280-6509 .- 1600-0889. ; 59, s. 77-98
-
Tidskriftsartikel (refereegranskat)abstract
- A three-dimensional Chemistry Transport Model was used to study the meteorologically induced interannual variability and trends in deposition of sulphur and nitrogen as well as concentrations of surface ozone (O3), nitrogen dioxide (NO2) and particulate matter (PM) and its constituents over Europe during 1958–2001. The model was coupled to the meteorological reanalysis ERA40, produced at the European Centre for Medium-range Weather Forecasts. Emissions and boundary conditions of chemical compounds and PM were kept constant at present levels. The average European interannual variation, due to meteorological variability, ranges from 3% for O3, 5%for NO2, 9% for PM, 6–9% for dry deposition, to about 20% for wet deposition of sulphur and nitrogen. For the period 1979–2001 the trend in ozone, due to climate variability is increasing in central and southwestern Europe and decreasing in northeastern Europe, the trend in NO2 is approximately opposite. The trend in PM is positive in eastern Europe. There are negative trends in wet deposition in southwestern and central Europe and positive trends in dry deposition overall. A bias in ERA40 precipitation could be partly responsible for the trends. The variation and trends need to be considered when interpreting measurements and designing measurement campaigns.
|
|
| 3. |
- Artaxo, Paulo, et al.
(författare)
-
Tropical and Boreal Forest – Atmosphere Interactions : A Review
- 2022
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 74:1, s. 24-163
-
Forskningsöversikt (refereegranskat)abstract
- This review presents how the boreal and the tropical forests affect the atmosphere, its chemical composition, its function, and further how that affects the climate and, in return, the ecosystems through feedback processes. Observations from key tower sites standing out due to their long-term comprehensive observations: The Amazon Tall Tower Observatory in Central Amazonia, the Zotino Tall Tower Observatory in Siberia, and the Station to Measure Ecosystem-Atmosphere Relations at Hyytiäla in Finland. The review is complemented by short-term observations from networks and large experiments.The review discusses atmospheric chemistry observations, aerosol formation and processing, physiochemical aerosol, and cloud condensation nuclei properties and finds surprising similarities and important differences in the two ecosystems. The aerosol concentrations and chemistry are similar, particularly concerning the main chemical components, both dominated by an organic fraction, while the boreal ecosystem has generally higher concentrations of inorganics, due to higher influence of long-range transported air pollution. The emissions of biogenic volatile organic compounds are dominated by isoprene and monoterpene in the tropical and boreal regions, respectively, being the main precursors of the organic aerosol fraction.Observations and modeling studies show that climate change and deforestation affect the ecosystems such that the carbon and hydrological cycles in Amazonia are changing to carbon neutrality and affect precipitation downwind. In Africa, the tropical forests are so far maintaining their carbon sink.It is urgent to better understand the interaction between these major ecosystems, the atmosphere, and climate, which calls for more observation sites, providing long-term data on water, carbon, and other biogeochemical cycles. This is essential in finding a sustainable balance between forest preservation and reforestation versus a potential increase in food production and biofuels, which are critical in maintaining ecosystem services and global climate stability. Reducing global warming and deforestation is vital for tropical forests.
|
|
| 4. |
- Bardakov, Roman, et al.
(författare)
-
Transport and chemistry of isoprene and its oxidation products in deep convective clouds
- 2021
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 73:1, s. 1-21
-
Tidskriftsartikel (refereegranskat)abstract
- Deep convective clouds can transport trace gases from the planetary boundary layer into the upper troposphere where subsequent chemistry may impact aerosol particle formation and growth. In this modelling study, we investigate processes that affect isoprene and its oxidation products injected into the upper troposphere by an isolated deep convective cloud in the Amazon. We run a photochemical box model with coupled cloud microphysics along hundreds of individual air parcel trajectories sampled from a cloud-resolving model simulation of a convective event. The box model simulates gas-phase chemical reactions, gas scavenging by liquid and ice hydrometeors, and turbulent dilution inside a deep convective cloud. The results illustrate the potential importance of gas uptake to anvil ice in regulating the intensity of the isoprene oxidation and associated low volatility organic vapour concentrations in the outflow. Isoprene transport and fate also depends on the abundance of lightning-generated nitrogen oxide radicals (NOx = NO + NO2). If gas uptake on ice is efficient and lightning activity is low, around 30% of the boundary layer isoprene will survive to the cloud outflow after approximately one hour of transport, while all the low volatile oxidation products will be scavenged by the cloud hydrometeors. If lightning NOx is abundant and gas uptake by ice is inefficient, then all isoprene will be oxidised during transport or in the immediate outflow region, while several low volatility isoprene oxidation products will have elevated concentrations in the cloud outflow. Reducing uncertainties associated with the uptake of vapours on ice hydrometeors, especially HO2 and oxygenated organics, is essential to improve predictions of isoprene and its oxidation products in deep convective outflows and their potential contribution to new particle formation and growth.
|
|
| 5. |
|
|
| 6. |
|
|
| 7. |
- Björkman, Mats P., et al.
(författare)
-
Nitrate dry deposition in svalbard
- 2013
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 65, s. 19071-
-
Tidskriftsartikel (refereegranskat)abstract
- Arctic regions are generally nutrient limited, receiving an extensive part of their bio-available nitrogen from the deposition of atmospheric reactive nitrogen. Reactive nitrogen oxides, as nitric acid (HNO3) and nitrate aerosols (p-NO3), can either be washed out from the atmosphere by precipitation or dry deposited, dissolving to nitrate (NO3-). During winter, NO3- is accumulated in the snowpack and released as a pulse during spring melt. Quantification of NO3- deposition is essential to assess impacts on Arctic terrestrial ecology and for ice core interpretations. However, the individual importance of wet and dry deposition is poorly quantified in the high Arctic regions where in-situ measurements are demanding. In this study, three different methods are employed to quantify NO3- dry deposition around the atmospheric and ecosystem monitoring site, Ny-Alesund, Svalbard, for the winter season (September 2009 to May 2010): (1) A snow tray sampling approach indicates a dry deposition of -10.27 +/- 3.84 mg m(-2) (+/- S.E.); (2) A glacial sampling approach yielded somewhat higher values -30.68 +/- 12.00 mg m(-2); and (3) Dry deposition was also modelled for HNO3 and p-NO3 using atmospheric concentrations and stability observations, resulting in a total combined nitrate dry deposition of -10.76 +/- 1.26 mg m(-2). The model indicates that deposition primarily occurs via HNO3 with only a minor contribution by p-NO3. Modelled median deposition velocities largely explain this difference: 0.63 cm s(-1) for HNO3 while p-NO3 was 0.0025 and 0.16 cm s(-1) for particle sizes 0.7 and 7 mm, respectively. Overall, the three methods are within two standard errors agreement, attributing an average 14% (total range of 2-44%) of the total nitrate deposition to dry deposition. Dry deposition events were identified in association with elevated atmospheric concentrations, corroborating recent studies that identified episodes of rapid pollution transport and deposition to the Arctic.
|
|
| 8. |
- Blasing, T.J, et al.
(författare)
-
The annual cycle of fossil-fuel carbon dioxide emissions in the United States
- 2005
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 57:2, s. 107-115
-
Tidskriftsartikel (refereegranskat)abstract
- Time-series of estimated monthly carbon dioxide emissions from consumption of coal, petroleum and natural gas in the United States from 1981 to 2002 have been derived from energy consumption data. The data series for coal and natural gas each reveal a consistent seasonal pattern, with a winter peak for gas and two peaks (summer and winter) for coal. The annual cycle of total emissions has an amplitude of about 20 Tg-C, and is dominated by CO2 released from consumption of natural gas. Summation of the monthly estimates to obtain annual values reveals good agreement with other estimates of CO2 emissions. The varying proportions of CO2 emitted from each fuel type over the course of a year lead to an annual cycle in the carbon isotope ratio (δ13C), with a range of about 2 ‰. These monthly carbon emissions estimates should be helpful in understanding the carbon cycle by providing (1) monthly/seasonal input for carbon cycle models, (2) estimates of the annual cycle of the 13C isotope ratio in fossil-fuel CO2 emissions and (3) data at fine enough time intervals to investigate effects of seasonal climate variations and changes in seasonally dependent use patterns of certain appliances (e.g. air conditioners) on fossil-fuel carbon emissions.
|
|
| 9. |
- Bower, K. N., et al.
(författare)
-
ACE-2 HILLCLOUD. An overview of the ACE-2 ground-based cloud experiment
- 2000
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509. ; 52:2, s. 750-778
-
Tidskriftsartikel (refereegranskat)abstract
- The ACE-2 HILLCLOUD experiment was carried out on the island of Tenerife in June-July 1997 to investigate the interaction of the boundary layer aerosol with a hill cap cloud forming over a ridge to the north-east of the island. The cloud was used as a natural flow through reactor to investigate the dependence of the cloud microphysics and chemistry on the characteristics of the aerosols and trace gases entering cloud, and to simultaneously study the influence of the physical and chemical processes occurring within the cloud on the size distribution, chemical and hygroscopic properties of the aerosol exiting cloud. 5 major ground base sites were used, measuring trace gases and aerosols upwind and downwind of the cloud, and cloud microphysics and chemistry and interstitial aerosol and gases within the cloud on the hill. 8 intensive measurement periods or runs were undertaken during cloud events, (nocturnally for seven of the eight runs) and were carried out in a wide range of airmass conditions from clean maritime to polluted continental. Polluted air was characterised by higher than average concentrations of ozone (> 50 ppbv), fine and accumulation mode aerosols (> 3000 and > 1500 cm -3 , respectively) and higher aerosol mass loadings. Cloud droplet number concentrations N, increased from 50 cm -3 in background maritime air to > 2500 cm -3 in aged polluted continental air, a concentration much higher than had previously been detected. Surprisingly, N was seen to vary almost linearly with aerosol number across this range. The droplet aerosol analyser (DAA) measured higher droplet numbers than the corrected forward scattering spectrometer probe (FSSP) in the most polluted air, but at other times there was good agreement (FSSP = 0.95 DAA with an r 2 = 0.89 for N < 1200 cm -3 ). Background ammonia gas concentrations were around 0.3 ppbv even in air originating over the ocean, another unexpected but important result for the region. NO 2 was present in background concentrations of typically 15 pptv to 100 pptv and NO 3 . (the nitrate radical) was observed at night throughout. Calculations suggest NO 3 . losses were mainly by reaction with DMS to produce nitric acid. Low concentrations of SO 2 (~30 pptv), HNO 3 and HCl were always present. HNO 3 concentrations were higher in polluted episodes and calculations implied that these exceeded those which could be accounted for by NO 2 oxidation. It is presumed that nitric and hydrochloric acids were present as a result of outgassing from aerosol, the HNO 3 from nitrate rich aerosol transported into the region from upwind of Tenerife, and HCl from sea salt aerosol newly formed at the sea surface. The oxidants hydrogen peroxide and ozone were abundant (i.e., were well in excess over SO 2 throughout the experiment). Occasions of significant aerosol growth following cloud processing were observed, particularly in cleaner cases. Observations and modelling suggested this was due mainly to the take up of nitric acid, hydrochloric acid and ammonia by the smallest activated aerosol particles. On a few occasions a small contribution was made by the in-cloud oxidation of S(IV). The implications of these results from HILLCLOUD for the climatologically more important stratocumulus Marine Boundary Layer (MBL) clouds are considered.
|
|
| 10. |
|
|
| 11. |
- Brandefelt, Jenny, et al.
(författare)
-
Anthropogenic and biogenic winter sources of Arctic CO2 - a model study
- 2001
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 53:1, s. 10-21
-
Tidskriftsartikel (refereegranskat)abstract
- Long-range transport of anthropogenic and biogenic CO2 to a remote site in the Arctic is studied. A limited area, off-line, Eulerian atmospheric transport model is used, and the results are compared to the observed CO2 concentration at the Ny-Alesund International Arctic Research and Monitoring Facility. Inventories of anthropogenic CO2 emissions and estimates of biogenic CO2 emissions are used to investigate the respective impact of these emissions on Arctic CO2 variations during 4 winter months. A direct comparison of the modelled and observed concentrations reveals remarkably good timing in the modelled variations as compared to the observed variations for most of the time. The correlation of observed versus modelled CO2 concentration is significant at the 95% confidence level. The biogenic and the anthropogenic CO2 emissions are shown to have approximately equal influence on Arctic CO2 variations during winter. Europe is found to be the dominant source of anthropogenic CO2 Lit the monitoring station, while Siberia and Northern America have little influence on Arctic CO2. during the months studied. These results contradict Engardt and Holmen whose results indicate that the lower-Ob region in western Siberia has a large impact on Arctic CO2.
|
|
| 12. |
|
|
| 13. |
- Budhavant, Krishnakant, et al.
(författare)
-
Anthropogenic fine aerosols dominate the wintertime regime over the northern Indian Ocean
- 2018
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 70
-
Tidskriftsartikel (refereegranskat)abstract
- This study presents and evaluates the most comprehensive set to date of chemical, physical and optical properties of aerosols in the outflow from South Asia covering a full winter (Nov. 2014 - March 2015), here intercepted at the Indian Ocean receptor site of the Maldives Climate Observatory in Hanimaadhoo (MCOH). Cluster analysis of air-mass back trajectories for MCOH, combined with AOD and meteorological data, demonstrate that the wintertime northern Indian Ocean is strongly influenced by aerosols transported from source regions with three major wind regimes, originating from the Indo-Gangetic Plain (IGP), the Bay of Bengal (BoB) and the Arabian Sea (AS). As much as 97 +/- 3% of elemental carbon (EC) in the PM10 was also found in the fine mode (PM2.5). Other mainly anthropogenic constituents such as organic carbon (OC), non-sea-salt (nss) -K+, nss-SO42- and NH4+ were also predominantly in the fine mode (70-95%), particularly in the air masses from IGP. The combination at this large-footprint receptor observatory of consistently low OC/EC ratio (2.0 +/- 0.5), strong linear relationships between EC and OC as well as between nss-K+ and both OC and EC, suggest a predominance of primary sources, with a large biomass burning contribution. The particle number-size distributions for the air masses from IGP and BoB exhibited clear bimodal shapes within the fine fraction with distinct accumulation (0.1m0.03. Taken together, the aerosol pollution over the northern Indian Ocean in the dry season is dominated by a well-mixed long-range transported regime of the fine-mode aerosols largely from primary combustion origin.
|
|
| 14. |
- Bäckstrand, Kristina, et al.
(författare)
-
Non-methane volatile organic compound flux from a subarctic mire in Northern Sweden
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:2, s. 226-237
-
Tidskriftsartikel (refereegranskat)abstract
- Biogenic NMVOCs are mainly formed by plants and microorganisms. They have strong impact on the local atmospheric chemistry when emitted to the atmosphere. The objective of this study was to determine if there are significant emissions of non-methane volatile organic compounds (NMVOCs) from a subarctic mire in northern Sweden. Subarctic peatlands in discontinuous permafrost regions are undergoing substantial environmental changes due to their high sensitivity to climate warming and there is need for including NMVOCs in the overall carbon budget. Automatic and manual chamber measurements were used to estimate NMVOC fluxes from three dominating subhabitats on the mire during three growing seasons. Emission rates varied and were related to plant species distribution and seasonal net ecosystem exchange of carbon dioxide. The highest fluxes were observed from wetter sites dominated by Eriophorum and Sphagnum spp. Total NMVOC emissions from the mire (similar to 17 ha) is estimated to consist of similar to 150 kgC during a growing season with 150 d. NMVOC fluxes can account for similar to 5% of total net carbon exchange (-3177 kgC) at the mire during the same period. NMVOC emissions are therefore a significant component in a local carbon budget for peatlands.
|
|
| 15. |
- Börjesson, Gunnar, et al.
(författare)
-
A national landfill methane budget for Sweden based on field measurements, and an evaluation of IPCC models
- 2009
-
Ingår i: Tellus, Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 61:2, s. 424-435
-
Tidskriftsartikel (refereegranskat)abstract
- Seven Swedish landfills were investigated from 2001 to 2003. On each landfill, a measure of the total methane production was calculated from data on: (1) methane emissions (leakage); (2) methane oxidation and (3) from gas recovery. Methane emissions were determined via a tracer gas (N2O) release-based remote sensing method. N2O and CH4 were measured with an Fourier Transform infrared detector at a distance of more than 1 km downwind from the landfills. Methane oxidation in the landfill covers was measured with the stable carbon isotope method. The efficiency in gas recovery systems proved to be highly variable, but on an average, 51% of the produced landfill gas was captured. A first-order decay model, based on four fractions (waste from households and parks, sludges and industrial waste), showed that the use of a degradable organic carbon fraction (DOCf) value of 0.54, in accordance with the default value for DOCf of 0.50 in the latest IPCC model, gave an emission estimate similar to the official national reports.
|
|
| 16. |
- Böö, Sebastian, 1979-, et al.
(författare)
-
Transport of Mineral Dust Into the Arctic in Two Reanalysis Datasets of Atmospheric Composition
- 2023
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - 0280-6509 .- 1600-0889. ; 75:1, s. 13-32
-
Tidskriftsartikel (refereegranskat)abstract
- Two three-dimensional reanalysis datasets of atmospheric composition, the Copernicus Atmosphere Monitoring Service reanalysis (CAMSRA) and the Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2), are analyzed for the years 2003-2018 with respect to dust transport into the Arctic. The reanalyses agree on that the largest mass transport of dust into the Arctic occurs across western Russia during spring and early summer, but substantial transport events occasionally also occur across other geographical areas during all seasons. In many aspects, however, the reanalyses show considerable differences: the mass transport in MERRA-2 is substantially larger, more spread out, and occurs at higher altitudes than in CAMSRA, while the transport in CAMSRA is to a higher degree focused to well-defined events in space and time; the integrated mass transport of the 10 most intense 36-hour dust events in CAMSRA constitutes 6 % of the total integrated dust transport 2003-2018, whereas the corresponding value for MERRA-2 is only 1 %.Furthermore, we compare the reanalyses with surface measurements of dust in the Arctic and dust extinction retrievals from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) satellite data. This comparison indicates that CAMSRA underestimates the dust transport into the Arctic and that MERRA-2 likely overestimates it. The discrepancy between CAMSRA and MERRA-2 can partially be explained by the assimilation process where too little dust is assimilated in CAMSRA while in MERRA-2, the assimilation process increases the dust concentration in remote areas. Despite the profound differences between the reanalyses regarding dust transport into the Arctic, this study still brings new insights into the spatio-temporal distribution of the transport. We estimate the annual dust transport into the Arctic to be within the range 1.5-31 Tg, where the comparison with observations indicates that the lower end of the interval is less likely.
|
|
| 17. |
|
|
| 18. |
- Chen, Deliang, 1961, et al.
(författare)
-
Summary of a workshop on extreme weather events in a warming world organized by the Royal Swedish Academy of Sciences
- 2020
-
Ingår i: Tellus Series B-Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 72:1
-
Tidskriftsartikel (refereegranskat)abstract
- Climate change is not only about changes in means of climatic variables such as temperature, precipitation and wind, but also their extreme values which are of critical importance to human society and ecosystems. To inspire the Swedish climate research community and to promote assessments of international research on past and future changes in extreme weather events against the global climate change background, the Earth Science Class of the Royal Swedish Academy of Sciences organized a workshop entitled 'Extreme weather events in a warming world' in 2019. This article summarizes and synthesizes the key points from the presentations and discussions of the workshop on changes in floods, droughts, heat waves, as well as on tropical cyclones and extratropical storms. In addition to reviewing past achievements in these research fields and identifying research gaps with a focus on Sweden, future challenges and opportunities for the Swedish climate research community are highlighted.
|
|
| 19. |
- Coz Diego, Esther, et al.
(författare)
-
Morphology and state of mixture of atmospheric soot aggregates during the winter season over Southern Asia-a quantitative approach
- 2011
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 63:1, s. 107-116
-
Tidskriftsartikel (refereegranskat)abstract
- The atmospheric brown cloud phenomena characterized by a high content of soot and a large impact on the solar radiative heating especially affects the tropical Indian Ocean during the winter season. The present study focuses on morphological characteristics and state of mixture of soot aggregates during the winter season over India. Given are quantitative measures of size, morphology and texture on aggregates collected in air at two different sites: Sinhagad near Pune in India and Hanimaadhoo in Maldives. For the latter site two different synoptic patterns prevailed: advection of air from the Arabian region and from the Indian subcontinent, respectively. Aggregates collected at Sinhagad, were associated with open branched structures, characteristic of fresh emission and diameters between 220 and 460 nm. The Hanimaadhoo aggregates were associated with aged closed structures, smaller sizes (130-360 nm) and frequently contained inorganic inclusions. Those arriving from the Indian subcontinent were characterized by the presence of an additional organic layer that covered the aggregate structure. These organic coatings might be a reasonable explanation of the low average wash-out ratios of soot two to seven times lower than that of nss-SO(4)2- that have been reported for air flow arriving at Hanimaadhoo from the Indian subcontinent in winter.
|
|
| 20. |
- Dal Maso, Miikka, et al.
(författare)
-
Annual and interannual variation in boreal forest aerosol particle number and volume concentration and their connection to particle formation
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:4, s. 495-508
-
Tidskriftsartikel (refereegranskat)abstract
- We investigated size-resolved submicrometre aerosol particle number and volume concentration time series as well as aerosol dynamic parameters derived front Differential Mobility Particle Sizer (DMPS) measurements at five background stations in the Nordic boreal forest area. The stations in question were Aspvreten, Hyytiala and Uto in Southern Finland and Sweden, and Varrio and Pallas in the Finnish Lapland. The objective Of Our investigation was to identify and quantity annual and interannual variation observable in the time series. We found that the total number and mass concentrations were touch lower at the Lapland stations than at the southern stations and that the total particle number was strongly correlated to particle formation event frequency. The annual total number concentration followed the annual distribution of particle formation events at the Southern stations but much less clearly at the Lapland stations. The volume concentration was highest during summer, in line with higher condensation growth rates: this is in line with the assumption that a large part of the particle volume is produced by oxidized plant emissions. The decrease of sulphate emissions in Europe was not visible in our data set. Aerosol dynamic parameters such as condensation sink, condensation sink diameter and the power law exponent linking coagulation losses and condensation sink are presented to characterize the submicron Nordic background aerosol.
|
|
| 21. |
- Delmas, RJ, et al.
(författare)
-
Bomb-test Cl-36 measurements in Vostok snow (Antarctica) and the use of Cl-36 as a dating tool for deep ice cores
- 2004
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509. ; 56:5, s. 492-498
-
Tidskriftsartikel (refereegranskat)abstract
- A large pulse of atmospheric Cl-36 generated by a limited number of nuclear tests peaked in the late 1950s to early 1960s. The corresponding enhanced Cl-36 deposition is seen in various glaciological archives in the Northern Hemisphere. The profile of the bomb spike recorded in firn layers at Vostok Station, central East Antarctica. has been measured by employing accelerator mass spectrometry (AMS). The records obtained front two well-dated data sets collected in snow pits in 1997 and 1998 show a broad Cl-36 peak, beginning as early as the 1940s and reaching its maximum in the 1960s. The signal is followed by a long-lasting tail up to the surface. This pattern is totally unexpected. We show that the results, unlike the Greenland data, can be explained by a mobility of HCl in the Antarctic firn. This experiment demonstrates the instability of gaseous Cl- deposits. a phenomenon which has important implications for the use of natural cosmogenic Cl-36 radionuclides as a reliable dating tool for deep ice cores from low-accumulation areas. However, during glacial times, under favourable atmospheric chemistry conditions this dating method may still be applicable. Snow metamorphism and ventilation are assumed to be the two main physical processes responsible for the observed patterns.
|
|
| 22. |
|
|
| 23. |
- Devasthale, Abhay, et al.
(författare)
-
The vertical distribution of thin features over the Arctic analysed from CALIPSO observations : Part 1: Optically thin clouds
- 2011
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 63:1, s. 77-85
-
Tidskriftsartikel (refereegranskat)abstract
- Clouds play a crucial role in the Arctic climate system. Therefore, it is essential to accurately and reliably quantify and understand cloud properties over the Arctic. It is also important to monitor and attribute changes in Arctic clouds. Here, we exploit the capability of the CALIPSO-CALIOP instrument and provide comprehensive statistics of tropospheric thin clouds, otherwise extremely difficult to monitor from passive satellite sensors. We use 4 yr of data (June 2006-May 2010) over the circumpolar Arctic, here defined as 67-82 degrees N, and characterize probability density functions of cloud base and top heights, geometrical thickness and zonal distribution of such cloud layers, separately for water and ice phases, and discuss seasonal variability of these properties. When computed for the entire study area, probability density functions of cloud base and top heights and geometrical thickness peak at 200-400, 1000-2000 and 400-800 m, respectively, for thin water clouds, while for ice clouds they peak at 6-8, 7-9 and 400-1000 m, respectively. In general, liquid clouds were often identified below 2 km during all seasons, whereas ice clouds were sensed throughout the majority of the upper troposphere and also, but to a smaller extent, below 2 km for all seasons.
|
|
| 24. |
- Dipu, Sudhakar, et al.
(författare)
-
Exploring Satellite-Derived Relationships between Cloud Droplet Number Concentration and Liquid Water Path Using a Large-Domain Large-Eddy Simulation
- 2022
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 74:1, s. 176-188
-
Tidskriftsartikel (refereegranskat)abstract
- Important aspects of the adjustments to aerosol-cloud interactions can be examined using the relationship between cloud droplet number concentration (Nd) and liquid water path (LWP). Specifically, this relation can constrain the role of aerosols in leading to thicker or thinner clouds in response to adjustment mechanisms. This study investigates the satellite retrieved relationship between Nd and LWP for a selected case of mid-latitude continental clouds using high-resolution Large-eddy simulations (LES) over a large domain in weather prediction mode. Since the satellite retrieval uses the adiabatic assumption to derive the Nd, we have also considered adiabatic Nd (NAd) from the LES model for comparison. The joint histogram analysis shows that the NAd-LWP relationship in the LES model and the satellite is in approximate agreement. In both cases, the peak conditional probability (CP) is confined to lower NAd and LWP; the corresponding mean LWP (LWP) shows a weak relation with NAd. The CP shows a larger spread at higher NAd (>50 cm–3), and the LWP increases non-monotonically with increasing NAd in both cases. Nevertheless, both lack the negative NAd-LWP relationship at higher NAd, the entrainment effect on cloud droplets. In contrast, the model simulated Nd-LWP clearly illustrates a much more nonlinear (an increase in LWP with increasing Nd and a decrease in LWP at higher Nd) relationship, which clearly depicts the cloud lifetime and the entrainment effect. Additionally, our analysis demonstrates a regime dependency (marine and continental) in the NAd-LWP relation from the satellite retrievals. Comparing local vs large-scale statistics from satellite data shows that continental clouds exhibit only a weak nonlinear NAd-LWP relationship. Hence a regime-based Nd-LWP analysis is even more relevant when it comes to warm continental clouds and their comparison to satellite retrievals.
|
|
| 25. |
- Engardt, M., et al.
(författare)
-
Deposition of sulphur and nitrogen in Europe 1900-2050. Model calculations and comparison to historical observations
- 2017
-
Ingår i: Tellus, Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 69:1, s. Article: 1328945-
-
Tidskriftsartikel (refereegranskat)abstract
- As a contribution to an EU project which dealt with the effects of climate change, air pollution impacts and ecosystems, two different atmospheric chemical transport models were used to simulate the depositions of acidifying and eutrophying pollutants over Europe for the period 1900-2050. Given the unavoidable uncertainties in the historical inputs to these simulations (emissions, meteorology), we generated a new and unique data-set for the purposes of model evaluation; comprising data from the European Air Chemistry Network (EACN) in operation from 1955 to early 1980s and more recent data from the EMEP monitoring network. The two models showed similar and reasonable skills in reproducing both the EACN and EMEP observational data although the MATCH model consistently simulates higher concentrations and depositions than the EMEP model. To further assess the models' ability to reproduce the long-term trend in sulphur and nitrogen deposition we compared modelled concentrations of major ions in precipitation with data extracted from a glacier in the European Alps. While, the shape and timing of the nss-sulphate data agrees reasonably, the ice core data indicate persistently high nitrogen concentrations of oxidised and reduced nitrogen after the 1980s which does not correspond to the model simulations or data from Western Europe in the EMEP monitoring network. This study concludes that nss-sulphate deposition to Europe was already clearly elevated in the year 1900, but has now (mid-2010s) decreased to about 70% of what it was at the beginning of the last century. The deposition of oxidised nitrogen to Europe peaked during the 1980s but has since decreased to half of its maximum value; still it is 3-4 times higher than in the year 1900. The annual deposition of reduced nitrogen to Europe is currently more than two times as high as the conditions in the year 1900.
|
|
| 26. |
- Engström, Anders, et al.
(författare)
-
Geographically coherent patterns of albedo enhancement and suppression associated with aerosol sources and sinks
- 2015
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 67, s. 1-9
-
Tidskriftsartikel (refereegranskat)abstract
- Earth's albedo is the primary determinant of the amount of energy absorbed by the Earth-atmosphere system. It is a function of the fractional cloud cover and the cloudy-and clear-sky albedos, and thereby of the aerosol loading of the atmosphere. Here, we introduce a method by which we can examine the spatial distribution of the albedo variability that is independent of variations in the two dominant factors of albedo: cloud fraction and liquid water path (LWP). The analysis is based on data simultaneously retrieved from the CERES and MODIS instruments carried on board the Aqua satellite. We analysed the daily overpass data between July 2002 and June 2014 and showed that perturbations in albedo, accounting for variations induced by cloud fraction and LWP, display a coherent geographical pattern. Positive deviations occur in proximity to known anthropogenic aerosol sources, and negative deviations coincide with areas of intense precipitation, acting as aerosol sinks. A simple multiplication of the observed positive perturbations in albedo with the solar flux of 340Wm(-2) yields a magnitude of that effect of several watts per square meter locally. While the location and scale of the geographical pattern might suggest an anthropogenic contribution to the positive albedo perturbations, it is imperative to first carefully examine all other possible causal factors behind the perturbations. Finally, although we have not attempted a full calculation of detection limits, the analysis is capable of sensing very small changes in average albedo of the order of 0.003 out of a total albedo of the order of 0.3. Hence, the applied method might find utilisation in a variety of situations where there is a need to quantify small perturbations of a dependent variable in noisy global data sets.
|
|
| 27. |
- Engström, J. Erik, et al.
(författare)
-
Seasonal variability in atmospheric black carbon at three stations in South-Asia
- 2017
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 69
-
Tidskriftsartikel (refereegranskat)abstract
- Filter-based optical measurements of black carbon in air, a constituent of soot, have been determined with a 528 nm light source during the period from 1 June 2005 to 31 May 2009 on samples taken at Godavari in Nepal, Sinhagad in India and Hanimaadhoo in the Maldives. In order to reduce systematic errors due to the light scattering of non-absorbing particles co-deposited on the filter, such as inorganic salts and mineral dust, an additional sensor recording backscattered light was implemented. Two protocols of corrections (optical and chemical) were applied to the samples collected at the observatories. The Indian monsoon circulation with its two annual phases in combination with the location of the combustion sources and their contribution relative to other non-anthropogenic sources dominated the observed patterns of black carbon at two of the observatories: in India and the Maldives. The observatory in Nepal was however mainly influenced by combustion sources all year around concealing possible variability related to the monsoon circulation. At the receptor observatory in the Maldives, peak values in the black carbon absorption coefficient occurred during the winter season (December to April) when air was transported from the polluted Indian subcontinent out over the Indian Ocean. A close to two orders of magnitude lower values were recorded in air that had spent more than 10-days over the Indian Ocean during the monsoon season (July to September), suggested to be dominated by particulate matter from remote marine biogenic sources and not by combustion sources.
|
|
| 28. |
- Engvall, Ann-Christine, et al.
(författare)
-
In-situ airborne observations of the microphysical properties of the Arctic tropospheric aerosol during late spring and summer
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:3, s. 392-404
-
Tidskriftsartikel (refereegranskat)abstract
- In-situ aerosol data collected in the Arctic troposphere during a three-week period in 2004 were analysed. The measurements took place during late spring, i.e., at the time of the year when the characteristics of the aerosol distribution change from being accumulation-mode dominated to being primarily of the Aitken-mode type, a process that previously has been observed in the boundary layer. To address the question whether this transition is also detectable in the free troposphere of an aircraft-measured data from the ASTAR 2004 campaign were analysed. In this study, we present vertically as well as temporally results from both ground-based and airborne measurements of the total number concentrations of particles larger than 10 and 260 nm. Aircraft-measured size distributions of the aerosol ranging from 20 to 2200 nm have been evaluated with regard to conditions in the boundary layer as well as in the free troposphere. Furthermore an analysis of the volatile fraction of the aerosol population has been performed both for the integrated and size-distributed results. From these investigations we find that the transition takes place in the entire troposphere.
|
|
| 29. |
- Engvall, Ann-Christine, et al.
(författare)
-
The radiative effect of an aged, internally mixed Arctic aerosol originating from lower-latitude biomass burning
- 2009
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 61:4, s. 677-684
-
Tidskriftsartikel (refereegranskat)abstract
- Arctic-haze layers and their radiative effects have been investigated previously in numerous studies as they are known to have an impact on the regional climate. In this study, we report on an event of an elevated aerosol layer, notably consisting of high-absorbing soot particles, observed in the European Arctic free troposphere the 2007 April 14 during the ASTAR 2007 campaign. The ca. 0.5 km vertically thick aerosol layer located at an altitude of around 3 km had a particle-size distribution mode around 250 nm diameter. In this study, we quantify the radiative effect aerosol layers have on the Arctic atmosphere by using in situ observations. Measurements of particles size segregated temperature stability using thermal denuders, indicate that the aerosol in the optically active size range was chemically internally mixed. In the plume, maximum observed absorption and scattering coefficients were 3 x 10(-6) and 20 x 10(-6) m(-1), respectively. Observed microphysical and optical properties were used to constrain calculations of heating rates of an internally mixed aerosol assuming two different surface albedos that represent snow/ice covered and open ocean. The average profile resulted in a heating rate in the layer of 0.2 K d(-1) for the high-albedo case and 0.15 K d(-1) for the low albedo case. This calculated dependence on albedo based on actual observations corroborates previous numerical simulations. The heating within the plume resulted in a measurable signal shown as an enhancement in the temperature of a few tenths of a degree. Although the origin of the aerosol plume could not unambiguously be determined, the microphysical properties of the aerosol had strong similarities with previously reported biomass burning plumes. With a changing climate, short-lived pollutants such as biomass plumes may become more frequent in the Arctic and have important radiative effects at regional scale.
|
|
| 30. |
- Fleischer, Siegfried, 1938-, et al.
(författare)
-
Dark oxidation of water in soils
- 2013
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - Hoboken, NJ : Wiley-Blackwell. - 0280-6509 .- 1600-0889. ; 65:1
-
Tidskriftsartikel (refereegranskat)abstract
- We report the release of oxygen (O2) under dark conditions in aerobic soils. This unexpected process is hidden by respiration which constitutes the dominating reversal O2 flux. By using H218O in different soils, we confirmed that 16O18O and 18O2 released under dark soil conditions originated from added H218O. Water is the only large-scale source of electrons for reduction of CO2 in soils, but it has not been considered as an electron donor because of the very strong oxidation system needed. A high share of soil inorganic material seems to favor the release of O2. © 2013 S. Fleischer et al.
|
|
| 31. |
- Fleischer, Siegfried, 1938-, et al.
(författare)
-
Nitrogen cycling drives a strong within-soil CO2-sink
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - Oxford : Wiley-Blackwell. - 0280-6509 .- 1600-0889. ; 60:5, s. 782-786
-
Tidskriftsartikel (refereegranskat)abstract
- For about three decades, it has not been possible to completely balance global carbon emissions into known pools. A residual (or 'missing') sink remains. Here evidence is presented that part of soil respiration is allocated into an internal soil CO2-sink localized to the saprophytic subsystem (roots excluded). The process occurs in forest, agricultural and grassland soils and is favoured by high N-deposition. Chemoautotrophic nitrification has a key role, and the most efficient internal CO2-sequestration occurs concurrently with lowest soil nitrate (NO3-) concentrations, despite considerable N-loading. Not until drastic N-supply occurs, does the CO2-sink successively breakdown, and nitrate concentrations increase, leading to NO3--leaching. Within-soil CO2-uptake seems to be of the same magnitude as the missing carbon sink. It may be gradually enforced by the ongoing input of nitrogen to the biosphere.
|
|
| 32. |
- Flynn, Michael J., et al.
(författare)
-
Modelling cloud processing of aerosol during the ACE-2 HILLCLOUD experiment
- 2000
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509. ; 52:2, s. 779-800
-
Tidskriftsartikel (refereegranskat)abstract
- A numerical model has been used to simulate the conditions observed during the ACE-2 Hillcloud experiment and to study the processes which may be taking place. The model incorporates gas phase chemistry of sulphur and nitrogen compounds upstream of the cloud, and the interaction of aerosol, precursor trace gases and oxidants within the cloud. Gas phase and aerosol inputs to the model have been provided from measurements made in the field. Dynamics of the air flow over the hill consisted of simple prescribed dynamics based on wind speed measurements, and also for some cases modelled dynamics. In this modelling study, it was found that during clean case studies particles down to 40-55 nm diameter were activated to form cloud droplets, the total number of droplets formed ranging from 200 to 400 drops/cm3. Significant modification of the aerosol spectra due to cloud processing was observed. In polluted cases particles down to 65-80 nm diameter were activated to form cloud droplets, the total number of droplets ranging from 800 to 2800 drops/cm3. Modification of the aerosol spectra due to cloud processing was slight. In all cases, changes in the aerosol spectra were due to both the uptake of HNO3, HCl, NH3 and SO2 from the gas phase, (the SO2 being oxidised to sulphate) and the repartitioning of species such as HNO3, HCl, and NH3 from larger particles onto smaller ones. Modelling results have been compared with observations made. Modelled droplet numbers are typically within 20% of the best measured values. The mode of the droplet distribution typically around 10-20 μm for clean cases and 4-8 μm for polluted cases was found to be in good agreement with the measured values of 10-25 μm for clean cases, but not in such good agreement for polluted cases. Measurements of upwind and interstitial aerosol distributions showed that the smallest particles activated were 30 and 50 nm for clean and polluted cases respectively, slightly smaller than the model values quoted above. Measured upwind and downwind aerosol spectra showed similar modification to that predicted by the model in eight out of the eleven model runs carried out. Chemistry measurements also give general evidence for both the uptake of species from the gas phase, and repartitioning of species from large particles onto smaller ones, though comparisons for individual cases are more difficult. From this modelling study, it can be concluded that in general, in the remote environment the exchange of hydrochloric acid, nitric acid and ammonia between aerosol particles and take up from the gas phase in the vicinity of cloud may be a very important mechanism in regulating the evolution of the aerosol spectrum. Further, the much more linear relationship between cloud droplet and accumulation mode aerosol number, which was observed in the measurements made during the ACE-2 HILLCLOUD project is supported by these modelling results. The implications of this for the indirect effect will be explored in future work.
|
|
| 33. |
- Franke, Vera, et al.
(författare)
-
Chemical composition and source analysis of carbonaceous aerosol particles at a mountaintop site in central Sweden
- 2017
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 69
-
Tidskriftsartikel (refereegranskat)abstract
- The chemical composition of atmospheric particulate matter at Mt. angstrom reskutan, a mountaintop site in central Sweden, was analysed with a focus on its carbonaceous content. Filter samples taken during the Cloud and Aerosol Experiment at angstrom re (CAEsAR 2014) were analysed by means of a thermo-optical method and ion chromatography. Additionally, the particle light absorption and particle number size distribution measurements for the entire campaign were added to the analysis. Mean airborne concentrations of organic and elemental carbon during CAEsAR 2014 were OC= 0.85 +/- 0.8 mu gm(-3) and EC = 0.06 +/- 0.06 mu gm(-3), respectively. Elemental to organic carbon ratios varied between EC/OC = 0.02 and 0.19. During the study a large wildfire occurred in Vastmanland, Sweden, with the plume reaching our study site. This led to significant increases in OC and EC concentrations (OC = 3.04 +/- 0.03 mu gm(-3) and EC = 0.24 +/- 0.00 mu gm(-3)). The mean mass-specific absorption coefficient observed during the campaign was sigma(BC)(abs) = 9.1 +/- 7.3 m(2)g(-1) (at wavelength lambda= 637 nm). In comparison to similarly remote European sites, Mt. angstrom reskutan experienced significantly lower carbonaceous aerosol loadings with a clear dominance of organic carbon. A mass closure study revealed a missing chemical mass fraction that likely originated from mineral dust. Potential regional source contributions of the carbonaceous aerosol were investigated using modelled air mass back trajectories. This source apportionment pointed to a correlation between high EC concentrations and air originating from continental Europe. Particles rich in organic carbon most often arrived from highly vegetated continental areas. However, marine regions were also a source of these aerosol particles. The source contributions derived during this study were compared to emission inventories of an Earth system model. This comparison highlighted a lack of OC and EC point-sources in the model's emission inventory which could potentially lead to an underestimation of the carbonaceous aerosol reaching Mt. angstrom reskutan in the simulation of this Earth system model.
|
|
| 34. |
- Freud, E., et al.
(författare)
-
Anthropogenic aerosol effects on convective cloud microphysical properties in southern Sweden
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:2, s. 286-297
-
Tidskriftsartikel (refereegranskat)abstract
- In this study, we look for anthropogenic aerosol effects in southern Scandinavia's clouds under the influence of moderate levels of pollution and relatively weak dynamic forcing. This was done by comparing surface aerosol measurements with convective cloud microphysical profiles produced from satellite image analyses. The results show that the clouds associated with the anthropogenic-affected air with high PM0.5, had to acquire a vertical development of similar to 3.5 km before forming precipitation-sized particles, compared to less than 1 km for the clouds associated with low PM0.5 air-masses. Additionally, a comparison of profiles with precipitation was done with regard to different potentially important parameters. For precipitating clouds the variability of the cloud thickness needed to produce the precipitation (Delta h(14)) is directly related to PM0.5 concentrations, even without considering atmospheric stability, the specific aerosol size distribution or the aerosols' chemical composition. Each additional 1 mu g m(-3) of PM0.5 was found to increase Delta h(14) by similar to 200-250 m. Our conclusion is that it is indeed possible to detect the effects of anthropogenic aerosol on the convective clouds in southern Scandinavia despite modest aerosol masses. It also emphasizes the importance of including aerosol processes in climate-radiation models and in numerical weather prediction models.
|
|
| 35. |
- Frey, Lena, et al.
(författare)
-
Absorbing aerosols over Asia – an inter-model and model-observation comparison study using CAM5.3-Oslo
- 2021
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 73:1, s. 1-25
-
Tidskriftsartikel (refereegranskat)abstract
- Aerosol absorption constitutes a significant component of the total radiative effect of aerosols, and hence its representation in general circulation models is crucial to radiative forcing estimates. We use here multiple observations to evaluate the performance of CAM5.3-Oslo with respect to its aerosol representation. CAM5.3-Oslo is the atmospheric component of the earth system model NorESM1.2 and shows on average an underestimation of aerosol absorption in the focus region over East and South Asia and a strong aerosol absorption overestimation in desert and arid regions compared to observations and other AeroCom phase III models. We explore the reasons of the model spread and find that it is related to the column burden and residence time of absorbing aerosols, in particular black carbon and dust. We conduct further sensitivity simulations with CAM5.3-Oslo to identify processes which are most important for modelled aerosol absorption. The sensitivity experiments target aerosol optical properties, and contrast their impact with effects from changes in emissions and deposition processes, and the driving meteorology. An improved agreement with observations was found with the use of a refined emission data set, transient emissions and assimilation of meteorological observations. Changes in optical properties of absorbing aerosols can also reduce the under- and overestimation of aerosol absorption in the model. However, changes in aerosol absorption strength between the sensitivity experiments are small compared to the inter-model spread among the AeroCom phase III models.
|
|
| 36. |
- Friberg, Johan, et al.
(författare)
-
Sources of increase in lowermost stratospheric sulphurous and carbonaceous aerosol background concentrations during 1999-2008 derived from CARIBIC flights
- 2014
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889.
-
Tidskriftsartikel (refereegranskat)abstract
- This study focuses on sulphurous and carbonaceous aerosol, the major constituents of particulate matter in the lowermost stratosphere (LMS), based on in situ measurements from 1999 to 2008. Aerosol particles in the size range of 0.082 mm were collected monthly during intercontinental flights with the CARIBIC passenger aircraft, presenting the first long-term study on carbonaceous aerosol in the LMS. Elemental concentrations were derived via subsequent laboratory-based ion beam analysis. The stoichiometry indicates that the sulphurous fraction is sulphate, while an O/C ratio of 0.2 indicates that the carbonaceous aerosol is organic. The concentration of the carbonaceous component corresponded on average to approximately 25% of that of the sulphurous, and could not be explained by forest fires or biomass burning, since the average mass ratio of Fe to K was 16 times higher than typical ratios in effluents from biomass burning. The data reveal increasing concentrations of particulate sulphur and carbon with a doubling of particulate sulphur from 1999 to 2008 in the northern hemisphere LMS. Periods of elevated concentrations of particulate sulphur in the LMS are linked to downward transport of aerosol from higher altitudes, using ozone as a tracer for stratospheric air. Tropical volcanic eruptions penetrating the tropical tropopause are identified as the likely cause of the particulate sulphur and carbon increase in the LMS, where entrainment of lower tropospheric air into volcanic jets and plumes could be the cause of the carbon increase.
|
|
| 37. |
- Fuzzi, S., et al.
(författare)
-
The Po Valley Fog Experiment 1989
- 1992
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509. ; 44:5, s. 448-468
-
Tidskriftsartikel (refereegranskat)abstract
- An outline is presented here of the Po Valley Fog Experiment 1989, carried out within the EUROTRAC‐GCE project. This experiment is a joint effort by several European research groups from 5 countries. The physical and chemical behaviour of the fog multiphase system was studied experimentally following the temporal evolution of the relevant chemical species in the different phases (gas, droplet, interstitial aerosol) and the evolution of micrometeorological and microphysical conditions, from the pre‐fog situation through the whole fog evolution, to the post‐fog period. Some general results, useful for describing the general features of the fog system, are presented here, while specific scientific questions on the different processes taking place within the system itself will be addressed in other companion papers of this same issue.
|
|
| 38. |
- Gallardo, L, et al.
(författare)
-
Could cloud-to-cloud discharges be as effective as cloud-to-ground discharges in producing NOx?
- 1996
-
Ingår i: TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY. - : MUNKSGAARD INT PUBL LTD. - 0280-6509. ; 48:5, s. 641-651
-
Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- In global models of tropospheric ozone and oxidized nitrogen, it is usually assumed that cloud-to-cloud discharges are 3 to 10 x less effective than cloud-to-ground discharges in producing nitrogen oxides (NOx). This assumption is based on a limited numbe
|
|
| 39. |
- Glantz, Paul, et al.
(författare)
-
Trends in MODIS and AERONET derived aerosol optical thickness over Northern Europe
- 2019
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 71:1
-
Tidskriftsartikel (refereegranskat)abstract
- Long-term Aqua and Terra MODIS (MODerate resolution Imaging Spectroradiometer) Collections 5.1 and 6.1 (c051 and c061, respectively) aerosol data have been combined with AERONET (AERosol RObotic NETwork) ground-based sun photometer observations to examine trends in aerosol optical thickness (AOT, at 550nm) over Northern Europe for the months April to September. For the 1927 and 1559 daily coincident measurements that were obtained for c051 and c061, respectively, MODIS AOT varied by 86 and 90%, respectively, within the predicted uncertainty of one standard deviation of the retrieval over land (AOT = +/- 0.05 +/- 0.15AOT). For the coastal AERONET site Gustav Dalen Tower (GDT), Sweden, larger deviations were found for MODIS c051 and c061 (79% and 75%, respectively, within predicted uncertainty). The Baltic Sea provides substantially better statistical representation of AOT than the surrounding land areas and therefore favours the investigations of trends in AOT over the region. Negative trends of 1.5% and 1.2% per year in AOT, based on daily averaging, were found for the southwestern Baltic Sea from MODIS c051 and c061, respectively. This is in line with a decrease of 1.2% per year in AOT at the AERONET station Hamburg. For the western Gotland Basin area, Sweden, negative trends of 1.5%, 1.1% and 1.6% per year in AOT have been found for MODIS c051, MODIS c061 and AERONET GDT, respectively. The strongest trend of -1.8% per year in AOT was found for AERONET Belsk, Poland, which can be compared to -1.5% per day obtained from MODIS c051 over central Poland. The trends in MODIS and AERONET AOT are nearly all statistically significant at the 95% confidence level. The strongest aerosol sources are suggested to be located southwest, south and southeast of the investigation area, although the highest prevalence of pollution events is associated with air mass transport from southwest.
|
|
| 40. |
- Graham, Emelie Linnéa, et al.
(författare)
-
Physical and chemical properties of aerosol particles and cloud residuals on Mt. angstrom reskutan in Central Sweden during summer 2014
- 2020
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 72:1
-
Tidskriftsartikel (refereegranskat)abstract
- The size distribution, volatility and hygroscopicity of ambient aerosols and cloud residuals were measured with a differential mobility particle sizer (DMPS) and a volatility-hygroscopicity tandem differential mobility analyser (VHTDMA) coupled to a counterflow virtual impactor (CVI) inlet during the Cloud and Aerosol Experiment at Are (CAEsAR) campaign at Mt. Areskutan during summer 2014. The chemical composition of particulate matter (PM) and cloud water were analysed offline using thermo-optical OC/EC analysis and ion chromatography. The importance of aerosol particle size for cloud droplet activation and subsequent particle scavenging was clearly visible in the measured size distributions. Cloud residuals were shifted towards larger sizes compared to ambient aerosol, and the cloud events were followed by a size distribution dominated by smaller particles. Organics dominated both PM (62% organic mass fraction) and cloud water (63% organic mass fraction) composition. The volatility and hygroscopicity of the ambient aerosols were representative of homogeneous aged aerosol with contributions from biogenic secondary organics, with median volume fraction remaining (VFR) of 0.04-0.05, and median hygroscopicity parameter kappa of 0.16-0.24 for 100-300 nm particles. The corresponding VFR and kappa for the cloud residuals were 0.03-0.04 and 0.18-0.20. The chemical composition, hygroscopicity and volatility measurements thus showed no major differences between the ambient aerosol particles and cloud residuals. The VFR and kappa values predicted based on the chemical composition measurements agreed well with the VHTDMA measurements, indicating the bulk chemical composition to be a reasonable approximation throughout the size distribution. There were indications, however, of some more subtle changes in time scales not achievable by the offline chemical analysis applied here. Further, online observations of aerosol and cloud residual chemical composition are therefore warranted.
|
|
| 41. |
- Grelle, A., et al.
(författare)
-
Large carbon-sink potential by Kyoto forests in Sweden - A case study on willow plantations
- 2007
-
Ingår i: Tellus Series B-Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 59:5, s. 910-918
-
Tidskriftsartikel (refereegranskat)abstract
- Fluxes of CO were measured in a 75-ha short-rotation willow plantation at Enkoping, central Sweden. The plantation was irrigated with wastewater for fertilization and water-filtering purposes. The harvested biomass was used locally for combined heat and power production. The plantation was a sink of ca. 8 tonnes C ha(-1) during 2003, of which ca. 50% was estimated to be attributed to fertilization. Biomass increment by shoot growth was 5 tonnes C ha-1 during the same year. Belowground carbon allocation was estimated to 3 tonnes C ha(-1) yr(-1) by a model that relates carbon allocation to shoot growth. Thus, the ecosystem carbon balance was closed by these estimations. The carbon uptake by the willow plantation was 5.5 times as high compared to a normally managed spruce forest, but only half as high as from an experimental, well-roanaged willow plantation in the same region. This illustrates the vast potential of short-rotation willow plantations for CO2 uptake from the atmosphere.
|
|
| 42. |
- GuðlaugsdÓttir, Hera, et al.
(författare)
-
North Atlantic weather regimes in δ18O of winter precipitation : isotopic fingerprint of the response in the atmospheric circulation after volcanic eruptions
- 2019
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 71:1, s. 1-19
-
Tidskriftsartikel (refereegranskat)abstract
- Equatorial volcanic eruptions are known to impact the atmospheric circulation on seasonal time scales through a strengthening of the stratospheric zonal winds followed by dynamic ocean-atmosphere coupling. This emerges as the positive phase of the North Atlantic Oscillation in the first 5 years after an eruption. In the North Atlantic, other modes of atmospheric circulation contribute to the climate variability but their response to volcanic eruptions has been less studied. We address this by retrieving the stable water isotopic fingerprint of the four major atmospheric circulation modes over the North Atlantic (Atlantic Ridge, Scandinavian Blocking and the negative and positive phases of the North Atlantic Oscillation (NAO − and NAO+)) by using monthly precipitation data from Global Network of Isotopes in Precipitation (GNIP) and 500 mb geo-potential height from the 20th Century Reanalysis. The simulated stable isotopic pattern of each atmospheric circulation mode is further used to assess the retrieved pattern. We test if changes in the atmospheric circulation as well as moisture source conditions as a result of volcanic eruptions can be identified by analyzing the winter climate response after both equatorial and high-latitude North Hemispheric volcanic eruptions in data, reanalysis and simulations. We report of an NAO + mode in the first two years after equatorial eruptions followed by NAO − in year 3 due to a decrease in the meridional temperature gradient as a result of volcanic surface cooling. This emerges in both GNIP data as well as reanalysis. Although the detected response is stronger after equatorial eruptions compared to high latitude eruptions, our results show that the response after high latitude eruptions tend to emerge as NAO − in year 2 followed by NAO + in year 3–4.
|
|
| 43. |
- Hegg, Dean A., et al.
(författare)
-
Measurements of black carbon aerosol washout ratio on Svalbard
- 2011
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 63:5, s. 891-900
-
Tidskriftsartikel (refereegranskat)abstract
- Simultaneous measurements of aerosol black carbon (BC) in both fresh snow and in air on Svalbard are presented. From these, washout ratios for BC are calculated and compared to sparse previous measurements of this metric in the arctic. The current ratios are significantly higher than previously found measured values. We argue that the degree of snow riming within the accretion zone can explain most of this difference. Using an analytical model of the scavenging process, BC scavenging efficiencies are estimated to lie in the range 0.25-0.5, comparable to measured values.
|
|
| 44. |
|
|
| 45. |
- Hermann, M, et al.
(författare)
-
Submicrometer aerosol particle distributions in the upper troposphere over the mid-latitude North Atlantic - Results from the third route of 'CARIBIC'
- 2008
-
Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:1, s. 106-117
-
Tidskriftsartikel (refereegranskat)abstract
- Particle number and mass concentrations of submicrometer aerosol particles were determined for the upper troposphere over the mid-latitude North Atlantic within the Civil Aircraft for Regular Investigation of the Atmosphere Based on an Instrument Container project (CARIBIC, http://www.caribic-atmospheric.com). Between May 2001 and April 2002, 22 flights from Germany to the Caribbean were conducted using an automated measurement container on a B767 passenger aircraft. Spatial and seasonal probability distributions for ultrafine and Aitken mode particles as well as mass concentrations of particulate sulphur in 8-12 km altitude are presented. High particle number concentrations (mostly 2500-15 000 particles cm(-3) STP) are particularly found in summer over the western North Atlantic Ocean close to the North American continent. The distributions together with an analysis of particle source processes show that deep vertical transport is the dominant process leading to most of the events with high particle number concentrations (greater than or similar to 8000 particles cm(-3) STP) for ultrafine particles as well as for Aitken mode particles. This study emphasizes the importance of deep vertical transport and cloud processing for the concentration of aerosol particles in the upper troposphere.
|
|
| 46. |
|
|
| 47. |
- Hieronymus, Jenny, 1981-, et al.
(författare)
-
Unravelling the land source : an investigation of the processes contributing to the oceanic input of DIC and alkalinity
- 2013
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 65, s. 19683-
-
Tidskriftsartikel (refereegranskat)abstract
- In models of the marine carbon system, it is important to correctly represent riverine and aerial inputs of dissolved inorganic carbon (DIC) and alkalinity. We have examined the different processes contributing to this exchange. In terms of DIC, we have divided the fluxes into their internal component, constituting the carbon ultimately derived from the atmosphere, and their external component originating from rocks. We find that the only process contributing to external DIC input is carbonate and fossil carbon weathering and that erosion of organic matter ultimately constitutes a DIC sink. A number of both riverine and aerial inputs affect the alkalinity. Beside carbonate and silicate weathering, we examine processes of pyrite weathering, aerial input of sulphuric acid, and riverine and aerial inputs of various nitrogen species. Using the observation that, in the ocean, the nitrate concentration follows that of phosphate, we assume a steady state in nitrate. This leads to the surprising result that the only processes affecting the alkalinity is riverine input of nitrate, constituting an alkalinity source and input of ammonia, constituting an alkalinity sink. Furthermore, we compare the flux sizes. As expected, carbonate and silicate weathering has the largest effect on alkalinity, though we note that burial of pyrite might be of importance during periods of large-scale anoxia.
|
|
| 48. |
- Hogg, A., et al.
(författare)
-
Stomatal and non-stomatal fluxes of ozone to a northern mixed hardwood forest
- 2007
-
Ingår i: Tellus Series B-Chemical and Physical Meteorology. - 0280-6509. ; 59:3, s. 514-525
-
Tidskriftsartikel (refereegranskat)abstract
- Measurements of ozone, sensible heat, and latent heat fluxes and plant physiological parameters were made at a northern mixed hardwood forest located at the University of Michigan Biological Station in northern Michigan from June 27 to September 28, 2002. These measurements were used to calculate total ozone flux and partitioning between stomatal and non-stomatal sinks. Total ozone flux varied diurnally with maximum values reaching 100 mu mol m(-2) h(-1) at midday and minimums at or near zero at night. Mean daytime canopy conductance was 0.5 mol m(-2) s(-1). During daytime, non-stomatal ozone conductance accounted for as much as 66% of canopy conductance, with the non-stomatal sink representing 63% of the ozone flux. Stomatal conductance showed expected patterns of behaviour with respect to photosynthetic photon flux density (PPFD) and vapour pressure defecit (VPD). Non-stomatal conductance for ozone increased monotonically with increasing PPFD, increased with temperature (T) before falling off again at high T, and behaved similarly for VPD. Day-time non-stomatal ozone sinks are large and vary with time and environmental drivers, particularly PPFD and T. This information is crucial to deriving mechanistic models that can simulate ozone uptake by different vegetation types.
|
|
| 49. |
- Horst, Axel, et al.
(författare)
-
Stable bromine isotopic composition of atmospheric CH3Br
- 2013
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 65, s. 21040-
-
Tidskriftsartikel (refereegranskat)abstract
- Tropospheric methyl bromide (CH3Br) is the largest source of bromine to the stratosphere and plays an important role in ozone depletion. Here, the first stable bromine isotope composition (delta Br-81) of atmospheric CH3Br is presented. The delta Br-81 of higher concentration Stockholm samples and free air subarctic Abisko samples suggest a source/background value of -0.04 +/- 0.28 parts per thousand ranging up to +1.75 +/- 0.12 parts per thousand. The Stockholm delta Br-81 versus concentration relationship corresponds to an apparent isotope enrichment factor of -4.7 +/- 3.7 parts per thousand, representing the combined reaction sink. This study demonstrates the scientific potential of atmospheric delta Br-81 measurements, which in the future may be combined with other isotope systems in a top-down inverse approach to further understand key source and sink processes of methyl bromide.
|
|
| 50. |
- Hussein, Tareq, et al.
(författare)
-
Observation of regional new particle formation in the urban atmosphere
- 2008
-
Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:4, s. 509-521
-
Tidskriftsartikel (refereegranskat)abstract
- Long-term measurements of fine particle number-size distributions were carried out over 9.5 yr (May 1997-December 2006), in the urban background atmosphere of Helsinki. The total number of days was 3528 with about 91.9% valid data. A new particle formation event (NPF) is defined if a distinct nucleation mode of aerosol particles is observed below 25 nm for several hours, and it shows a growth pattern. We observed 185 NPF events, 111 d were clear non-events and most of the days (around 83.5%) were undefined. The observed events were regional because they were observed at Hyytiala (250 km north of Helsinki). The events occurred most frequently during spring and autumn. The observed formation rate was maximum during the spring and summer (monthly median 2.87 cm(-3) s(-1)) and the modal growth rate was maximum during late summer and Autumn (monthly median 6.55 mm h(-1)). The events were observed around noon, and the growth pattern often continued on the following day. The observation of weak NPF events was hindered due to pre-existing particles from both local sources. It is clear that regional NPF events have a clear influence oil the dynamic behaviour of aerosol particles in the urban atmosphere.
|
|
