9 results
Search Results
Now showing 1 - 9 of 9
- ItemInfluences of the 2010 Eyjafjallajökull volcanic plume on air quality in the northern Alpine region(München : European Geopyhsical Union, 2011) Schäfer, K.; Thomas, W.; Peters, A.; Ries, L.; Obleitner, F.; Schnelle-Kreis, J.; Birmili, W.; Diemer, J.; Fricke, W.; Junkermann, W.; Pitz, M.; Emeis, S.; Forkel, R.; Suppan, P.; Flentje, H.; Gilge, S.; Wichmann, H.E.; Meinhardt, F.; Zimmermann, R.; Weinhold, K.; Soentgen, J.; Münkel, C.; Freuer, C.; Cyrys, J.A series of major eruptions of the Eyjafjallajökull volcano in Iceland started on 14 April 2010 and continued until the end of May 2010. The volcanic emissions moved over nearly the whole of Europe and were observed first on 16 April 2010 in Southern Germany with different remote sensing systems from the ground and space. Enhanced PM10 and SO2 concentrations were detected on 17 April at mountain stations (Zugspitze/Schneefernerhaus and Schauinsland) as well as in Innsbruck by in situ measurement devices. On 19 April intensive vertical mixing and advection along with clear-sky conditions facilitated the entrainment of volcanic material down to the ground. The subsequent formation of a stably stratified lower atmosphere with limited mixing near the ground during the evening of 19 April led to an additional enhancement of near-surface particle concentrations. Consequently, on 19 April and 20 April exceedances of the daily threshold value for particulate matter (PM10) were reported at nearly all monitoring stations of the North Alpine foothills as well as at mountain and valley stations in the northern Alps. The chemical analyses of ambient PM10 at monitoring stations of the North Alpine foothills yielded elevated Titanium concentrations on 19/20 April which prove the presence of volcanic plume material. Following this result the PM10 threshold exceedances are also associated with the volcanic plume. The entrainment of the volcanic plume material mainly affected the concentrations of coarse particles (>1 μm) – interpreted as volcanic ash – and ultrafine particles (<100 nm), while the concentrations of accumulation mode aerosol (0.1–1 μm) were not changed significantly. With regard to the occurrence of ultrafine particles, it is concluded that their formation was triggered by high sulphuric acid concentrations which are necessarily generated by the photochemical processes in a plume rich in sulphur dioxide under high solar irradiance. It became evident that during the course of several days, the Eyjafjallajökull volcanic emissions influenced the near-surface atmosphere and thus the ambient air quality. Although the volcanic plume contributed to the overall exposure of the population of the northern Alpine region on two days, only minor effects on the exacerbation of respiratory and cardiovascular symptoms can be expected.
- ItemAerosol decadal trends - Part 2: In-situ aerosol particle number concentrations at GAW and ACTRIS stations(München : European Geopyhsical Union, 2013) Asmi, A.; Collaud Coen, M.; Ogren, J.A.; Andrews, E.; Sheridan, P.; Jefferson, A.; Weingartner, E.; Baltensperger, U.; Bukowiecki, N.; Lihavainen, H.; Kivekäs, N.; Asmi, E.; Aalto, P.P.; Kulmala, M.; Wiedensohler, A.; Birmili, W.; Hamed, A.; O'Dowd, C.; Jennings, S.G.; Weller, R.; Flentje, H.; Fjaeraa, A.M.; Fiebig, M.; Myhre, C.L.; Hallar, A.G.; Swietlicki, E.; Kristensson, A.; Laj, P.We have analysed the trends of total aerosol particle number concentrations (N) measured at long-term measurement stations involved either in the Global Atmosphere Watch (GAW) and/or EU infrastructure project ACTRIS. The sites are located in Europe, North America, Antarctica, and on Pacific Ocean islands. The majority of the sites showed clear decreasing trends both in the full-length time series, and in the intra-site comparison period of 2001–2010, especially during the winter months. Several potential driving processes for the observed trends were studied, and even though there are some similarities between N trends and air temperature changes, the most likely cause of many northern hemisphere trends was found to be decreases in the anthropogenic emissions of primary particles, SO2 or some co-emitted species. We could not find a consistent agreement between the trends of N and particle optical properties in the few stations with long time series of all of these properties. The trends of N and the proxies for cloud condensation nuclei (CCN) were generally consistent in the few European stations where the measurements were available. This work provides a useful comparison analysis for modelling studies of trends in aerosol number concentrations.
- ItemPollution events observed during CARIBIC flights in the upper troposphere between South China and the Philippines(München : European Geopyhsical Union, 2010) Lai, S.C.; Baker, A.K.; Schuck, T.J.; van Velthoven, P.; Oram, D.E.; Zahn, A.; Hermann, M.; Weigelt, A.; Slemr, F.; Brenninkmeijer, C.A.M.; Ziereis, H.A strong pollution episode in the upper troposphere between South China and the Philippines was observed during CARIBIC flights in April 2007. Five pollution events were observed, where enhancements in aerosol and trace gas concentrations including CO, CO2, CH4, non-methane hydrocarbons (NMHCs) and halocarbons were observed along the flight tracks during four sequential flights. The importance of the contribution of biomass/biofuel burning was investigated using chemical tracers, emission factor analysis, back-trajectory analysis and satellite images. The Indochinese peninsula was identified as the probable source region of biomass/biofuel burning. However, enhancements in the urban/industrial tracer C2Cl4 during the events also indicate a substantial contribution from urban anthropogenic emissions. An estimation of the contribution of fossil fuel versus biomass/biofuel to the CO enhancement was made, indicating a biomass/biofuel burning contribution of ~54 to ~92% of the observed CO enhancements. Biomass/biofuel burning was found to be the most important source category during the sampling period.
- ItemAerosol optical properties in the North China Plain during HaChi campaign: An in-situ optical closure study(München : European Geopyhsical Union, 2011) Ma, N.; Zhao, C.S.; Nowak, A.; Müller, T.; Pfeifer, S.; Cheng, Y.F.; Deng, Z.Z.; Liu, P.F.; Xu, W.Y.; Ran, L.; Yan, P.; Göbel, T.; Hallbauer, E.; Mildenberger, K.; Henning, S.; Yu, J.; Chen, L.L.; Zhou, X.J.; Stratmann, F.; Wiedensohler, A.The largest uncertainty in the estimation of climate forcing stems from atmospheric aerosols. In early spring and summer of 2009, two periods of in-situ measurements on aerosol physical and chemical properties were conducted within the HaChi (Haze in China) project at Wuqing, a town between Beijing and Tianjin in the North China Plain (NCP). Aerosol optical properties, including the scattering coefficient (σsp), the hemispheric back scattering coefficient (σbsp), the absorption coefficient (σap), as well as the single scattering albedo (ω), are presented. The diurnal and seasonal variations are analyzed together with meteorology and satellite data. The mean values of σsp, 550 nm of the dry aerosol in spring and summer are 280±253 and 379±251 Mm−1, respectively. The average σap for the two periods is respectively 47±38 and 43±27 Mm−1. The mean values of ω at the wavelength of 637 nm are 0.82±0.05 and 0.86±0.05 for spring and summer, respectively. The relative high levels of σsp and σbsp are representative of the regional aerosol pollution in the NCP. Pronounced diurnal cycle of $σsp, σap and ω are found, mainly influenced by the evolution of boundary layer and the accumulation of local emissions during nighttime. The pollutants transported from the southwest of the NCP are more significant than that from the two megacities, Beijing and Tianjin, in both spring and summer. An optical closure experiment is conducted to better understand the uncertainties of the measurements. Good correlations (R>0.98) are found between the values measured by the nephelometer and the values calculated with a modified Mie model. The Monte Carlo simulation shows an uncertainty of about 30 % for the calculations. Considering all possible uncertainties of measurements, calculated σsp and σbsp agree well with the measured values, indicating a stable performance of instruments and thus reliable aerosol optical data.
- ItemEvaluation of biospheric components in earth system models using modern and palaeo-observations: The state-of-the-art(München : European Geopyhsical Union, 2013) Foley, A.M.; Dalmonech, D.; Friend, A.D.; Aires, F.; Archibald, A.T.; Bartlein, P.; Bopp, L.; Chappellaz, J.; Cox, P.; Edwards, N.R.; Feulner, G.; Friedlingstein, P.; Harrison, S.P.; Hopcroft, P.O.; Jones, C.D.; Kolassa, J.; Levine, J.G.; Prentice, I.C.; Pyle, J.; Vázquez Riveiros, N.; Wolff, E.W.; Zaehle, S.Earth system models (ESMs) are increasing in complexity by incorporating more processes than their predecessors, making them potentially important tools for studying the evolution of climate and associated biogeochemical cycles. However, their coupled behaviour has only recently been examined in any detail, and has yielded a very wide range of outcomes. For example, coupled climate–carbon cycle models that represent land-use change simulate total land carbon stores at 2100 that vary by as much as 600 Pg C, given the same emissions scenario. This large uncertainty is associated with differences in how key processes are simulated in different models, and illustrates the necessity of determining which models are most realistic using rigorous methods of model evaluation. Here we assess the state-of-the-art in evaluation of ESMs, with a particular emphasis on the simulation of the carbon cycle and associated biospheric processes. We examine some of the new advances and remaining uncertainties relating to (i) modern and palaeodata and (ii) metrics for evaluation. We note that the practice of averaging results from many models is unreliable and no substitute for proper evaluation of individual models. We discuss a range of strategies, such as the inclusion of pre-calibration, combined process- and system-level evaluation, and the use of emergent constraints, that can contribute to the development of more robust evaluation schemes. An increasingly data-rich environment offers more opportunities for model evaluation, but also presents a challenge. Improved knowledge of data uncertainties is still necessary to move the field of ESM evaluation away from a "beauty contest" towards the development of useful constraints on model outcomes.
- ItemEmerging pattern of global change in the upper atmosphere and ionosphere(München : European Geopyhsical Union, 2008) Laštovička, J.; Akmaev, R.A.; Beig, G.; Bremer, J.; Emmert, J.T.; Jacobi, C.; Jarvis, M.J.; Nedoluha, G.; Portnyagin, Yu. I.In the upper atmosphere, greenhouse gases produce a cooling effect, instead of a warming effect. Increases in greenhouse gas concentrations are expected to induce substantial changes in the mesosphere, thermosphere, and ionosphere, including a thermal contraction of these layers. In this article we construct for the first time a pattern of the observed long-term global change in the upper atmosphere, based on trend studies of various parameters. The picture we obtain is qualitative, and contains several gaps and a few discrepancies, but the overall pattern of observed long-term changes throughout the upper atmosphere is consistent with model predictions of the effect of greenhouse gas increases. Together with the large body of lower atmospheric trend research, our synthesis indicates that anthropogenic emissions of greenhouse gases are affecting the atmosphere at nearly all altitudes between ground and space.
- ItemNitrate radicals and biogenic volatile organic compounds: Oxidation, mechanisms, and organic aerosol(München : European Geopyhsical Union, 2017) Ng, Nga Lee; Brown, Steven S.; Archibald, Alexander T.; Atlas, Elliot; Cohen, Ronald C.; Crowley, John N.; Day, Douglas A.; Donahue, Neil M.; Fry, Juliane L.; Fuchs, Hendrik; Griffin, Robert J.; Guzman, Marcelo I.; Herrmann, Hartmut; Hodzic, Alma; Iinuma, Yoshiteru; Jimenez, José L.; Kiendler-Scharr, Astrid; Lee, Ben H.; Luecken, Deborah J.; Mao, Jingqiu; McLaren, Robert; Mutzel, Anke; Osthoff, Hans D.; Ouyang, Bin; Picquet-Varrault, Benedicte; Platt, Ulrich; Pye, Havala O.T.; Rudich, Yinon; Schwantes, Rebecca H.; Shiraiwa, Manabu; Stutz, Jochen; Thornton, Joel A.; Tilgner, Andreas; Williams, Brent J.; Zaveri, Rahul A.Oxidation of biogenic volatile organic compounds (BVOC) by the nitrate radical (NO3) represents one of the important interactions between anthropogenic emissions related to combustion and natural emissions from the biosphere. This interaction has been recognized for more than 3 decades, during which time a large body of research has emerged from laboratory, field, and modeling studies. NO3-BVOC reactions influence air quality, climate and visibility through regional and global budgets for reactive nitrogen (particularly organic nitrates), ozone, and organic aerosol. Despite its long history of research and the significance of this topic in atmospheric chemistry, a number of important uncertainties remain. These include an incomplete understanding of the rates, mechanisms, and organic aerosol yields for NO3-BVOC reactions, lack of constraints on the role of heterogeneous oxidative processes associated with the NO3 radical, the difficulty of characterizing the spatial distributions of BVOC and NO3 within the poorly mixed nocturnal atmosphere, and the challenge of constructing appropriate boundary layer schemes and non-photochemical mechanisms for use in state-of-the-art chemical transport and chemistry–climate models. This review is the result of a workshop of the same title held at the Georgia Institute of Technology in June 2015. The first half of the review summarizes the current literature on NO3-BVOC chemistry, with a particular focus on recent advances in instrumentation and models, and in organic nitrate and secondary organic aerosol (SOA) formation chemistry. Building on this current understanding, the second half of the review outlines impacts of NO3-BVOC chemistry on air quality and climate, and suggests critical research needs to better constrain this interaction to improve the predictive capabilities of atmospheric models.
- ItemN2O emissions from the global agricultural nitrogen cycle – current state and future scenarios(München : European Geopyhsical Union, 2012) Bodirsky, B.L.; Popp, A.; Weindl, I.; Dietrich, J.P.; Rolinski, S.; Scheiffele, L.; Schmitz, C.; Lotze-Campen, H.Reactive nitrogen (Nr) is not only an important nutrient for plant growth, thereby safeguarding human alimentation, but it also heavily disturbs natural systems. To mitigate air, land, aquatic, and atmospheric pollution caused by the excessive availability of Nr, it is crucial to understand the long-term development of the global agricultural Nr cycle. For our analysis, we combine a material flow model with a land-use optimization model. In a first step we estimate the state of the Nr cycle in 1995. In a second step we create four scenarios for the 21st century in line with the SRES storylines. Our results indicate that in 1995 only half of the Nr applied to croplands was incorporated into plant biomass. Moreover, less than 10 per cent of all Nr in cropland plant biomass and grazed pasture was consumed by humans. In our scenarios a strong surge of the Nr cycle occurs in the first half of the 21st century, even in the environmentally oriented scenarios. Nitrous oxide (N2O) emissions rise from 3 Tg N2O-N in 1995 to 7–9 in 2045 and 5–12 Tg in 2095. Reinforced Nr pollution mitigation efforts are therefore required.
- ItemObservation-based modelling of permafrost carbon fluxes with accounting for deep carbon deposits and thermokarst activity(München : European Geopyhsical Union, 2015) Schneider von Deimling, T.; Grosse, G.; Strauss, J.; Schirrmeister, L.; Morgenstern, A.; Schaphoff, S.; Meinshausen, M.; Boike, J.High-latitude soils store vast amounts of perennially frozen and therefore inert organic matter. With rising global temperatures and consequent permafrost degradation, a part of this carbon stock will become available for microbial decay and eventual release to the atmosphere. We have developed a simplified, two-dimensional multi-pool model to estimate the strength and timing of future carbon dioxide (CO2) and methane (CH4) fluxes from newly thawed permafrost carbon (i.e. carbon thawed when temperatures rise above pre-industrial levels). We have especially simulated carbon release from deep deposits in Yedoma regions by describing abrupt thaw under newly formed thermokarst lakes. The computational efficiency of our model allowed us to run large, multi-centennial ensembles under various scenarios of future warming to express uncertainty inherent to simulations of the permafrost carbon feedback. Under moderate warming of the representative concentration pathway (RCP) 2.6 scenario, cumulated CO2 fluxes from newly thawed permafrost carbon amount to 20 to 58 petagrams of carbon (Pg-C) (68% range) by the year 2100 and reach 40 to 98 Pg-C in 2300. The much larger permafrost degradation under strong warming (RCP8.5) results in cumulated CO2 release of 42 to 141 Pg-C and 157 to 313 Pg-C (68% ranges) in the years 2100 and 2300, respectively. Our estimates only consider fluxes from newly thawed permafrost, not from soils already part of the seasonally thawed active layer under pre-industrial climate. Our simulated CH4 fluxes contribute a few percent to total permafrost carbon release yet they can cause up to 40% of total permafrost-affected radiative forcing in the 21st century (upper 68% range). We infer largest CH4 emission rates of about 50 Tg-CH4 per year around the middle of the 21st century when simulated thermokarst lake extent is at its maximum and when abrupt thaw under thermokarst lakes is taken into account. CH4 release from newly thawed carbon in wetland-affected deposits is only discernible in the 22nd and 23rd century because of the absence of abrupt thaw processes. We further show that release from organic matter stored in deep deposits of Yedoma regions crucially affects our simulated circumpolar CH4 fluxes. The additional warming through the release from newly thawed permafrost carbon proved only slightly dependent on the pathway of anthropogenic emission and amounts to about 0.03–0.14 °C (68% ranges) by end of the century. The warming increased further in the 22nd and 23rd century and was most pronounced under the RCP6.0 scenario, adding 0.16 to 0.39 °C (68% range) to simulated global mean surface air temperatures in the year 2300.