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  • 1
    In: International Journal of Pancreatology, Springer Science and Business Media LLC, Vol. 16, No. 2-3 ( 1994-10), p. 183-310
    Type of Medium: Online Resource
    ISSN: 1537-3649 , 1559-0739
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1994
    detail.hit.zdb_id: 2466657-9
    detail.hit.zdb_id: 2103370-5
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  • 2
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 21, No. 22 ( 2021-11-23), p. 16925-16953
    Abstract: Abstract. Primary ice formation in mixed-phase clouds is initiated by a minute subset of the ambient aerosol population, called ice-nucleating particles (INPs). The knowledge about their atmospheric concentration, composition, and source in cloud-relevant environments is still limited. During the 2017 joint INUIT/CLACE (Ice Nuclei research UnIT/CLoud–Aerosol Characterization Experiment) field campaign, observations of INPs as well as of aerosol physical and chemical properties were performed, complemented by source region modeling. This aimed at investigating the nature and sources of INPs. The campaign took place at the High-Altitude Research Station Jungfraujoch (JFJ), a location where mixed-phase clouds frequently occur. Due to its altitude of 3580 m a.s.l., the station is usually located in the lower free troposphere, but it can also receive air masses from terrestrial and marine sources via long-range transport. INP concentrations were quasi-continuously detected with the Horizontal Ice Nucleation Chamber (HINC) under conditions representing the formation of mixed-phase clouds at −31 ∘C. The INP measurements were performed in parallel to aerosol measurements from two single-particle mass spectrometers, the Aircraft-based Laser ABlation Aerosol MAss Spectrometer (ALABAMA) and the laser ablation aerosol particle time-of-flight mass spectrometer (LAAPTOF). The chemical identity of INPs is inferred by correlating the time series of ion signals measured by the mass spectrometers with the time series of INP measurements. Moreover, our results are complemented by the direct analysis of ice particle residuals (IPRs) by using an ice-selective inlet (Ice-CVI) coupled with the ALABAMA. Mineral dust particles and aged sea spray particles showed the highest correlations with the INP time series. Their role as INPs is further supported by source emission sensitivity analysis using atmospheric transport modeling, which confirmed that air masses were advected from the Sahara and marine environments during times of elevated INP concentrations and ice-active surface site densities. Indeed, the IPR analysis showed that, by number, mineral dust particles dominated the IPR composition (∼58 %), and biological and metallic particles are also found to a smaller extent (∼10 % each). Sea spray particles are also found as IPRs (17 %), and their fraction in the IPRs strongly varied according to the increased presence of small IPRs, which is likely due to an impact from secondary ice crystal formation. This study shows the capability of combining INP concentration measurements with chemical characterization of aerosol particles using single-particle mass spectrometry, source region modeling, and analysis of ice residuals in an environment directly relevant for mixed-phase cloud formation.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2022
    In:  Boundary-Layer Meteorology Vol. 185, No. 1 ( 2022-10), p. 129-160
    In: Boundary-Layer Meteorology, Springer Science and Business Media LLC, Vol. 185, No. 1 ( 2022-10), p. 129-160
    Abstract: Lagrangian particle dispersion models (LPDMs) are frequently used for regional-scale inversions of greenhouse gas emissions. However, the turbulence parameterizations used in these models were developed for coarse resolution grids, hence, when moving to the kilometre-scale the validity of these descriptions should be questioned. Here, we analyze the influence of the turbulence parameterization employed in the LPDM FLEXPART-COSMO model. Comparisons of the turbulence kinetic energy between the turbulence schemes of FLEXPART-COSMO and the underlying Eulerian model COSMO suggest that the dispersion in FLEXPART-COSMO suffers from a double-counting of turbulent elements when run at a high resolution of $$1 \times 1 \,\hbox {km}^2$$ 1 × 1 km 2 . Such turbulent elements are represented in both COSMO, by the resolved grid-scale winds, and FLEXPART, by its stochastic parameterizations. Therefore, we developed a new parametrization for the variations of the winds and the Lagrangian time scales in FLEXPART in order to harmonize the amount of turbulence present in both models. In a case study for a power plant plume, the new scheme results in improved plume representation when compared with in situ flight observations and with a tracer transported in COSMO. Further in-depth validation of the LPDM against methane observations at a tall tower site in Switzerland shows that the model’s ability to predict the observed tracer variability and concentration at different heights above ground is considerably enhanced using the updated turbulence description. The high-resolution simulations result in a more realistic and pronounced diurnal cycle of the tracer concentration peaks and overall improved correlation with observations when compared to previously used coarser resolution simulations (at 7 km $$\times $$ × 7 km). Our results indicate that the stochastic turbulence schemes of LPDMs, developed in the past for coarse resolution models, should be revisited to include a resolution dependency and resolve only the part of the turbulence spectrum that is a subgrid process at each different mesh size. Although our new scheme is specific to COSMO simulations at $$1 \times 1 \,\hbox {km}^2$$ 1 × 1 km 2 resolution, the methodology for deriving the scheme can easily be applied to different resolutions and other regional models.
    Type of Medium: Online Resource
    ISSN: 0006-8314 , 1573-1472
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2022
    detail.hit.zdb_id: 242879-9
    detail.hit.zdb_id: 1477639-X
    SSG: 16,13
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  • 4
    In: CHIMIA, Swiss Chemical Society, Vol. 74, No. 3 ( 2020-03-25), p. 136-
    Abstract: CFCs (chlorofluorocarbons) and other strong ozone-depleting halogenated organic trace gases were used in numerous industrial, household and agriculture applications. First atmospheric measurements of CFCs were performed in the 1970s, well ahead of the detection of the ozone hole in the 1980s. The continuous observation of these ozone-depleting substances (ODSs) is crucial for monitoring their global ban within the Montreal Protocol. In addition, also HFCs (fluorinated hydrocarbons) are measured, which were introduced as substitutes of ODSs and are potent greenhouse gases. Since 2000, Empa continuously measures more than 50 halogenated trace gases at the high-Alpine station of Jungfraujoch (3850 m asl) as part of the global AGAGE network (Advanced Global Atmospheric Gases Experiment). Jungfraujoch is the highest location worldwide where such measurements are performed, and the site where several of these compounds were measured in the atmosphere for the first time. The measurements at Jungfraujoch and at other globally well-positioned sites serve as an early warning system, i. e. before potentially harmful halogenated organic substances can accumulate and detrimentally affect the natural environment.
    Type of Medium: Online Resource
    ISSN: 2673-2424 , 0009-4293
    RVK:
    Language: Unknown
    Publisher: Swiss Chemical Society
    Publication Date: 2020
    detail.hit.zdb_id: 2179192-2
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  • 5
    Online Resource
    Online Resource
    American Meteorological Society ; 2008
    In:  Journal of Applied Meteorology and Climatology Vol. 47, No. 11 ( 2008-11-01), p. 2946-2962
    In: Journal of Applied Meteorology and Climatology, American Meteorological Society, Vol. 47, No. 11 ( 2008-11-01), p. 2946-2962
    Abstract: The meteorological conditions at the Mount Kenya (station identifier MKN) tropical Global Atmosphere Watch Programme station are described. Like other stations in mountainous terrain, the site experiences thermally induced wind systems that disturb free tropospheric conditions. Therefore, the adequacy of the site for long-term background atmospheric composition measurements needs to be evaluated. Meteorological parameters for the period June 2002–June 2006 were analyzed, focusing on the development of thermally induced wind systems and boundary layer influence. Filters based on the local wind and day–night differences in specific humidity were developed for selection of times representative of undisturbed free tropospheric conditions. In addition, the convective boundary layer depth was evaluated. Throughout the whole year the station is influenced by thermally induced wind systems and the atmospheric boundary layer. The filters distinguished between thermally and synoptically influenced days. Thermally influenced days (86%) dominated. However, maxima in specific humidity were also reached in the afternoon on synoptically influenced days and were attributed to mixing in the convective boundary layer. During nighttime, downslope wind dominated that carries undisturbed free tropospheric air masses. Nevertheless, during 24% of all nights the specific humidity was also elevated, possibly indicating the presence of residual layers. It is recommended that nighttime data only (2100–0400 UTC) be used for analysis of long-term trends of the free tropospheric background while the remaining data can be used to characterize composition and trends of the regional atmospheric boundary layer. Further exclusion of apparent pollution events and residual layer influence should be considered. With these constraints, the Mount Kenya Global Atmosphere Watch site is adequate for the study of trends and budgets of background atmospheric composition.
    Type of Medium: Online Resource
    ISSN: 1558-8432 , 1558-8424
    RVK:
    Language: English
    Publisher: American Meteorological Society
    Publication Date: 2008
    detail.hit.zdb_id: 2227779-1
    detail.hit.zdb_id: 2227759-6
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  • 6
    Online Resource
    Online Resource
    American Meteorological Society ; 2005
    In:  Journal of Applied Meteorology Vol. 44, No. 5 ( 2005-05-01), p. 620-633
    In: Journal of Applied Meteorology, American Meteorological Society, Vol. 44, No. 5 ( 2005-05-01), p. 620-633
    Abstract: Elevated moisture layers in the lower free troposphere (2000–6000 m MSL) in the lee of the Alps were investigated. Specific humidity was analyzed within a Lagrangian concept for fair-weather days during a 12-yr period at the windward and the leeward sides of the Alps for the sounding sites of Payerne, Switzerland, and Milan, Italy. During daytime fair-weather conditions (different criteria), specific humidity increased significantly in air masses that advected from Payerne to Milan in a layer ranging from ∼2500 to 4000 m MSL. The maximum relative increase of specific humidity in this layer was ∼0.3, meaning that ∼30% of the air in this layer originated from the Alpine atmospheric boundary layer. On average, ∼30% of the mass of the Alpine boundary layer was vented to altitudes higher than 2500 m MSL per hour during the daytime. The total precipitable water within a layer reaching from 2500 to 3500 m MSL increased by ∼1.3 mm. Similar elevated layers were observed for different selection methods of fair-weather days, and climatologically for the whole of June, July, and August. Average observations of the relative increase and boundary layer export rate agree with results from the local case studies. Daytime thermally driven flow systems seem to be the main source of additional water vapor in the observed elevated layers over the Alps. Subsequently, horizontal advection toward flat terrain where the average ABL top was well below the elevated layer bottom results in the export of ABL air to the free troposphere (mountain venting). Mountain venting was enhanced in situations with larger global radiation, lower atmospheric stability, and additional moist convection as was detected by lightning activity.
    Type of Medium: Online Resource
    ISSN: 1520-0450 , 0894-8763
    Language: English
    Publisher: American Meteorological Society
    Publication Date: 2005
    detail.hit.zdb_id: 242493-9
    detail.hit.zdb_id: 2027356-3
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  • 7
    In: Biogeosciences, Copernicus GmbH, Vol. 13, No. 9 ( 2016-05-03), p. 2623-2635
    Abstract: Abstract. The understanding of the continental carbon budget is essential to predict future climate change. In order to quantify CO2 and CH4 fluxes at the regional scale, a measurement system was installed at the former radio tower in Beromünster as part of the Swiss greenhouse gas monitoring network (CarboCount CH). We have been measuring the mixing ratios of CO2, CH4 and CO on this tower with sample inlets at 12.5, 44.6, 71.5, 131.6 and 212.5 m above ground level using a cavity ring down spectroscopy (CRDS) analyzer. The first 2-year (December 2012–December 2014) continuous atmospheric record was analyzed for seasonal and diurnal variations and inter-species correlations. In addition, storage fluxes were calculated from the hourly profiles along the tower. The atmospheric growth rates from 2013 to 2014 determined from this 2-year data set were 1.78 ppm yr−1, 9.66 ppb yr−1 and −1.27 ppb yr−1 for CO2, CH4 and CO, respectively. After detrending, clear seasonal cycles were detected for CO2 and CO, whereas CH4 showed a stable baseline suggesting a net balance between sources and sinks over the course of the year. CO and CO2 were strongly correlated (r2 〉 0.75) in winter (DJF), but almost uncorrelated in summer. In winter, anthropogenic emissions dominate the biospheric CO2 fluxes and the variations in mixing ratios are large due to reduced vertical mixing. The diurnal variations of all species showed distinct cycles in spring and summer, with the lowest sampling level showing the most pronounced diurnal amplitudes. The storage flux estimates exhibited reasonable diurnal shapes for CO2, but underestimated the strength of the surface sinks during daytime. This seems plausible, keeping in mind that we were only able to calculate the storage fluxes along the profile of the tower but not the flux into or out of this profile, since no Eddy covariance flux measurements were taken at the top of the tower.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2158181-2
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  • 8
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 16, No. 13 ( 2016-07-11), p. 8341-8351
    Abstract: Abstract. Nucleation of ice affects the properties of clouds and the formation of precipitation. Quantitative data on how ice nucleating particles (INPs) determine the distribution, occurrence and intensity of precipitation are still scarce. INPs active at −8 °C (INPs−8) were observed for 2 years in precipitation samples at the High-Altitude Research Station Jungfraujoch (Switzerland) at 3580 m a.s.l. Several environmental parameters were scanned for their capability to predict the observed abundance and variability of INPs−8. Those singularly presenting the best correlations with observed number of INPs−8 (residual fraction of water vapour, wind speed, air temperature, number of particles with diameter larger than 0.5 µm, season, and source region of particles) were implemented as potential predictor variables in statistical multiple linear regression models. These models were calibrated with 84 precipitation samples collected during the first year of observations; their predictive power was successively validated on the set of 15 precipitation samples collected during the second year. The model performing best in calibration and validation explains more than 75 % of the whole variability of INPs−8 in precipitation and indicates that a high abundance of INPs−8 is to be expected whenever high wind speed coincides with air masses having experienced little or no precipitation prior to sampling. Such conditions occur during frontal passages, often accompanied by precipitation. Therefore, the circumstances when INPs−8 could be sufficiently abundant to initiate the ice phase in clouds may frequently coincide with meteorological conditions favourable to the onset of precipitation events.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 9
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 22, No. 4 ( 2022-02-23), p. 2447-2466
    Abstract: Abstract. Halocarbons contribute to global warming and stratospheric ozone depletion. They are emitted to the atmosphere by various anthropogenic activities. To determine Swiss national halocarbon emissions, we applied top-down methods, which rely on atmospheric concentration observations sensitive to the targeted emissions. We present 12 months (September 2019 to August 2020) of continuous atmospheric observations of 28 halocarbons from a measurement campaign at the Beromünster tall tower in Switzerland. The site is sensitive to the Swiss Plateau, which is the most densely populated area of Switzerland. Therefore, the measurements are well suited to derive Swiss halocarbon emissions. Emissions were calculated by two different top-down methods, i.e. a tracer ratio method (TRM), with carbon monoxide (CO) as the independent tracer, and a Bayesian inversion (BI), based on atmospheric transport simulations using FLEXPART–COSMO. The results were compared to previously reported top-down emission estimates, based on measurements at the high-Alpine site of Jungfraujoch, and to the bottom-up Swiss national greenhouse gas (GHG) inventory, as annually reported to the United Nations Framework Convention on Climate Change (UNFCCC). We observed moderately elevated concentrations of chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs), both banned from production and consumption in Europe. The corresponding emissions are likely related to the ongoing outgassing from older foams and refrigerators and confirm the widespread historical use of these substances. For the major hydrofluorocarbons (HFCs), HFC-125 (CHF2CF3) and HFC-32 (CH2F2), our calculated emissions of 100 ± 34 and 45 ± 14 Mg yr−1 are in good agreement with the numbers reported in the Swiss inventory, whereas, for HFC-134a (CH2FCF3), our result of 280 ± 89 Mg yr−1 is more than 30 % lower than the Swiss inventory. For HFC-152a (CH3CHF2), our top-down result of 21 ± 5 Mg yr−1 is significantly higher than the number reported in the Swiss inventory. For the other investigated HFCs, perfluorocarbons (PFCs), SF6 and NF3, Swiss emissions were small and in agreement with the inventory. Finally, we present the first country-based emission estimates for three recently phased-in, unregulated hydrofluoroolefins (HFOs), HFO-1234yf (CF3CF=CH2), HFO-1234ze(E) ((E)-CF3CH=CHF), and HCFO-1233zd(E) ((E)-CF3CH=CHCl). For these three HFOs, we calculated Swiss emissions of 15 ± 4, 34 ± 14, and 7 ± 1 Mg yr−1, respectively.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 10
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 20, No. 11 ( 2020-06-05), p. 6495-6519
    Abstract: Abstract. Atmospheric nitrous oxide (N2O) levels have been continuously growing since preindustrial times. Mitigation requires information about sources and sinks on the regional and global scales. Isotopic composition of N2O in the atmosphere could contribute valuable constraints. However, isotopic records of N2O in the unpolluted atmosphere remain too scarce for large-scale N2O models. Here, we report the results of discrete air samples collected weekly to biweekly over a 5-year period at the high-altitude research station Jungfraujoch, located in central Switzerland. High-precision N2O isotopic measurements were made using a recently developed preconcentration and laser spectroscopy technique. The measurements of discrete samples were accompanied by in situ continuous measurements of N2O mixing ratios. Our results indicate a pronounced seasonal pattern with minimum N2O mixing ratios in late summer, associated with a maximum in δ15Nbulk and a minimum in intramolecular 15N site preference (δ15NSP). This pattern is most likely due to stratosphere–troposphere exchange (STE), which delivers N2O-depleted but 15N-enriched air from the stratosphere into the troposphere. Variability in δ15NSP induced by changes in STE may be masked by biogeochemical N2O production processes in late summer, which are possibly dominated by a low-δ15NSP pathway of N2O production (denitrification), providing an explanation for the observed seasonality of δ15NSP. Footprint analyses and atmospheric transport simulations of N2O for Jungfraujoch suggest that regional emissions from the planetary boundary layer contribute to seasonal variations of atmospheric N2O isotopic composition at Jungfraujoch, albeit more clearly for δ15NSP and δ18O than for δ15Nbulk. With the time series of 5 years, we obtained a significant interannual trend for δ15Nbulk after deseasonalization (-0.052±0.012 ‰ a−1), indicating that the atmospheric N2O increase is due to isotopically depleted N2O sources. We estimated the average isotopic signature of anthropogenic N2O sources with a two-box model to be -8.6±0.6 ‰ for δ15Nbulk, 34.8±3 ‰ for δ18O and 10.7±4 ‰ for δ15NSP. Our study demonstrates that seasonal variation of N2O isotopic composition in the background atmosphere is important when determining interannual trends. More frequent, high-precision and interlaboratory-compatible measurements of atmospheric N2O isotopocules, especially for δ15NSP, are needed to better constrain anthropogenic N2O sources and thus the contribution of biogeochemical processes to N2O growth on the global scale.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2020
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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