Search

Measurements of H at the high-altitude site of Jungfraujoch, Switzerland are reported upon for the period of August, 2005-November, 2009. The time series consists of measurements that are primarily representative of free tropospheric background conditions. Highest background H mixing ratios were observed in May, while the lowest were observed in November. The mean seasonal H peak-to-trough amplitude of 21 parts per billion (ppb, 10 dry air mixing ratio) at Jungfraujoch was considerably less than at other stations at similar latitudes and the seasonal minimum in November was comparatively delayed. These differences are primarily attributed to a dampening and delay of the surface soil sink signal during its vertical propagation to the free troposphere. Excess (mixing ratio minus corresponding baseline value) H (ΔH) and excess CO (ΔCO) displayed no significant correlation. This lacking correlation is attributed to H removal by soil during transport to Jungfraujoch, thereby significantly altering the ΔH/ΔCO ratio from traffic combustion sources, which is the largest source of anthropogenic H influencing measurements at Jungfraujoch. [ABSTRACT FROM AUTHOR]

Anthropogenic halocarbons, such as chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), hydrofluorocarbons (HFCs), bromocarbons (halons) and long-lived chlorinated solvents have been measured continuously at the high-Alpine site of Jungfraujoch (Switzerland) since January 2000. Chloro- and bromo-containing halocarbons are responsible for the stratospheric ozone depletion and will be globally banned from usage within the next years. With the exception of the stable CFC-12 (CF2Cl2), all major CFCs and chlorinated solvents show a negative trend in recent years in their background concentrations at Jungfraujoch. HCFCs, as their first-generation substitute, are still increasing with a few percent per year. However, the frequency and the strength of HCFCs pollution events, which are caused by regional European emissions, are already declining. This can be seen as a sign of the impending ban of these gases within the next years in Europe. On the other hand, HFCs as the second-generation substitutes, are increasing with relative rates of at least 10% per year (e.g. almost 5 ppt per year for HFC-134a). An allocation of European sources was attempted by combining measured concentrations with trajectories of air masses reaching the Jungfraujoch during pollution events. Potential source regions could be detected in Italy, France, Spain and Germany. [Copyright &y& Elsevier]

A combination of reconstructed histories, long-term time series and recent quasi-continuous observations of non-CO2 greenhouse gases at the high-Alpine site Jungfraujoch is used to assess their current global radiative forcing budget and the influence of regulations due to the Montreal Protocol on Substances that Deplete the Ozone Layer in terms of climate change. Extrapolated atmospheric greenhouse gases trends from 1989 assuming a business-as-usual scenario, i.e. no Montreal Protocol restriction, are presented and compared to the observations. The largest differences between hypothetical business-as-usual mixing ratios and current atmospheric observations over the last 16 years were found for chlorinated species, in particular methyl chloroform (CH3CCl3) at 167 to 203 ppt and chlorofluorocarbon-12 (CFC-12) at 121 to 254 ppt. These prevented increases were used to estimate the effects of their restrictions on the radiative forcing budget. The net direct effect due to the Montreal Protocol regulations reduces global warming and offsets about 14 to 30% of the positive greenhouse effect related to the major greenhouse gases CO2, CH4, N2O and also SF6, and about 12 to 22% of the hypothetical current radiative forcing increase without Montreal Protocol restrictions. Thus, the Montreal Protocol succeeded not only in reducing the atmospheric chlorine content in the atmosphere but also dampened global warming. Nevertheless, the Montreal Protocol controlled species still add to global warming. [Copyright &y& Elsevier]

Abstract: Semi-continuous measurements of atmospheric molecular hydrogen and carbon monoxide (CO) were performed at a suburban sampling site in Switzerland from November 2002 to February 2005. The presented data provide information about time series, seasonal and diurnal cycles as well as sources and sinks in a suburban environment. Such records become increasingly important for the assessment of the effects of a possible future hydrogen economy on the environment. No significant trend of background concentrations could be observed for the considered period. Seasonal cycles show the expected pattern with maxima in winter and minima in summer and autumn. When extracting the background mixing ratios, the absolute levels as well as the seasonal amplitude agree well with literature data from semi-rural and remote sites. The dry deposition velocity for summer days with low winds is estimated to be between to . Diurnal cycles are dominated by emissions from nearby traffic. The influence of traffic-related emissions is also corroborated by a high to CO correlation. Typical molar to CO ratios from traffic were found to be 0. 33 on a molar basis (ppb/ppb). A reduction of 37–62% in European anthropogenic emissions is estimated for a period covering the last 25 years. Since the ambient concentration did not decline during the same period, other simultaneous changes of sinks or sources of must have compensated this reduction. [Copyright &y& Elsevier]

Ground-based in situ measurements of hydrofluorocarbons HFC-125, HFC-134a, and HFC-152a, which are regulated under the Kyoto Protocol, are carried out at four European sites within the SOGE (System of Observation of Halogenated Greenhouse Gases in Europe) program. Concentrations measured at the high mountain stations of Jungfraujoch (Switzerland) and Mte Cimone (Italy) together with back-trajectory statistical analysis are used in order to identify potential source regions on a European scale. Combining concentration data recorded at the two sites allows to reduce one of the problem which is inherent to the back-trajectory approach, i.e. the localisation of “ghost” sources in the wake of real sources. In this way, a more reliable picture of the location of European potential source regions is given. [Copyright &y& Elsevier]

The mixing ratios of HCFC-141b (1,1-dichlorofluoroethane) and HCFC-142b (1-chloro-1,1-difluoroethane) have been rising steadily in baseline air at Mace Head, Ireland over the 10-year period from 1994 to 2004. These HCFCs are widely used replacements for the chlorofluorocarbons phased out under the Montreal Protocol and its subsequent amendments. Analysis of the HCFC content of regionally-polluted air arriving at Mace Head from the European continent shows that European emissions reached a peak during 2000–2001 and have declined subsequently, following the phase-out in their usage. European emissions of HCFC-141b have been further constrained by observations at the High-Alpine Jungfraujoch site. The reductions are consistent with the phase-out of HCFC production and use from the year 2001 onwards mandated by European regulations designed to exceed the requirements of the Montreal Protocol. [Copyright &y& Elsevier]