| 1. |
- Andersson, Camilla, 1979-, et al.
(författare)
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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
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - Stockholm : Tellus. - 0280-6509 .- 1600-0889. ; 59, s. 77-98
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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.
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| 2. |
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| 3. |
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| 4. |
- Blasing, T.J, et al.
(författare)
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The annual cycle of fossil-fuel carbon dioxide emissions in the United States
- 2005
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 57:2, s. 107-115
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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.
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| 5. |
- Bäckstrand, Kristina, et al.
(författare)
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Non-methane volatile organic compound flux from a subarctic mire in Northern Sweden
- 2008
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:2, s. 226-237
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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.
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| 6. |
- Börjesson, Gunnar, et al.
(författare)
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A national landfill methane budget for Sweden based on field measurements, and an evaluation of IPCC models
- 2009
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Ingår i: Tellus, Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 61:2, s. 424-435
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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.
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| 7. |
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| 8. |
- Dal Maso, Miikka, et al.
(författare)
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Annual and interannual variation in boreal forest aerosol particle number and volume concentration and their connection to particle formation
- 2008
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:4, s. 495-508
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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.
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| 9. |
- Engvall, Ann-Christine, et al.
(författare)
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In-situ airborne observations of the microphysical properties of the Arctic tropospheric aerosol during late spring and summer
- 2008
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:3, s. 392-404
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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.
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| 10. |
- Engvall, Ann-Christine, et al.
(författare)
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The radiative effect of an aged, internally mixed Arctic aerosol originating from lower-latitude biomass burning
- 2009
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 61:4, s. 677-684
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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.
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