dot
Detailansicht
Katalogkarte GBA
Katalogkarte ISBD
Suche präzisieren
Drucken
Download RIS
Hier klicken, um den Treffer aus der Auswahl zu entfernen
Titel Investigations of the tropospheric halogen chemistry around Ross Island, Antarctica, during austral spring 2012
VerfasserIn Johannes Zielcke, Denis Pöhler, Udo Frieß, Tim Hay, Karin Kreher, Lars Kalnajs, Ulrich Platt
Konferenz EGU General Assembly 2013
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 15 (2013)
Datensatznummer 250081316
 
Zusammenfassung
A unique feature of the polar troposphere is the strong impact of halogen photochemistry, in which reactive halogen species (RHS) are responsible for ozone depletion as well as the oxidation of elemental mercury and dimethyl sulphide. The source, however, as well as release and recycling mechanisms of these halogen species are far from being completely understood, especially the role of chlorine and iodine compounds. Reactive chlorine, bromine and iodine compounds are thought to be released from sea salt particles or produced by the photolysis of halocarbons and I2 emitted by the ocean. Here we present observations of halogen oxides, ozone and nitrogen dioxide conducted for three months during austral spring 2012 on Ross Island, Antarctica. Measurements were performed with a suite of remote sensing instruments. An active long-path differential optical absorption spectroscopy (LP-DOAS) system was set up, measuring several species (BrO, O3, NO2, OBrO, IO, OIO, I2, ClO, OClO, CHOCHO, HCHO, HONO) continuously for the whole period, with two light paths over first year sea ice. In addition, a passive MAX-DOAS as well as a new Cavity-Enhanced (CE)-DOAS system were used for mobile halogen oxide measurements on a variety of locations around Ross Island (sea ice, shelf ice, snow, coastal, etc.), with top surface layer pH measurements performed at the different measurement sites. First results show highly variable ozone concentrations including partial Ozone Depletion Events (ODEs), as well as concentrations of BrO up to 16ppt and NO2 up to 15ppb. Suprisingly, a high variation of ozone was observed without significant amounts of BrO, indicating already depleted air masses transported to the measurement site and/or NOx chemistry inhibiting halogen radical reactions.