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Summertime NO<sub><i>y</i></sub> speciation at the Jungfraujoch, 3580 m above sea level, Switzerland
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References
2000
Year
EngineeringAtmospheric PhotochemistryAir QualityMarine ChemistryTotal Reactive NitrogenSummer 1997Reactive NitrogenEarth ScienceSocial SciencesEnvironmental ChemistryPaleoenvironmental ChangeBiogeographyMicrometeorologyAtmospheric SciencePleistoceneMeteorologyBiogeochemical CycleClimate DynamicsAir Pollution ClimatologyEvolutionary BiologyAtmospheric ProcessAir PollutionPaleoecologySea Level
During summer 1997, speciated reactive nitrogen (NO, NO 2 , peroxyacetyl nitrate (PAN), HNO 3 , and particulate nitrate) was measured in conjunction with total reactive nitrogen (NO y ) at the high‐alpine research station Jungfraujoch (JFJ), 3580 m above sea level (asl). The individually measured NO y components averaged to 82% of total NO y . PAN was the most abundant reactive nitrogen compound and composed on average 36% of NO y , followed by NO x , (22%), particulate nitrate (17%), and HNO 3 (7%). The NO x /NO y ratio averaged 0.25, but significantly lower values (0.15–0.20) were observed in the presence of high NO y mixing ratios. A classification of the data by synoptic weather conditions indicated that thermally driven vertical transport has a strong impact on the mixing ratios measured at the JFJ during summer. A strong diurnal cycle with maximum mixing ratios in the late afternoon was observed for convective days with north‐westerly advection at 500 hPa. In contrast, during a period of convective days with a wind speed below 7.5 m s −1 at 500 hPa, no obvious diurnal cycle was observed. Under these meteorological conditions the convective boundary layer can be significantly higher over the Alps (i.e., around 4 km asl) than over the surrounding lowlands. Subsequent advection may finally result in the export of reactive nitrogen reservoir compounds to the free troposphere and hence influence global atmospheric chemistry.
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