dot
Detailansicht
Katalogkarte GBA
Katalogkarte ISBD
Suche präzisieren
Drucken
Download RIS
Hier klicken, um den Treffer aus der Auswahl zu entfernen
Titel First measurements of continuous δ¹⁸O-CO2 with a Fourier Transform InfraRed spectrometer in Heidelberg, Germany
VerfasserIn Sanam Noreen Vardag, Samuel Hammer, David Griffith, Ingeborg Levin
Konferenz EGU General Assembly 2014
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 16 (2014)
Datensatznummer 250095574
Publikation (Nr.) Volltext-Dokument vorhandenEGU/EGU2014-11034.pdf
 
Zusammenfassung
Continuous in-situ measurements of δ13C and δ18O in atmospheric CO2 open the door to differentiating between different CO2 source and sink components with high temporal resolution. Until now only few instruments have been able to provide a continuous measurement of the oxygen isotope ratio in CO2. The Fourier Transform InfraRed (FTIR) spectrometer measures both the 13C/12C and 18O/16O ratios of CO2, but the precision and accuracy of the δ18O-CO2 measurements have not yet been evaluated. Here we present a first analysis of δ18O-CO2 measurements with an FTIR trace gas and isotope analyser in Heidelberg. We find that the spectrometer resolves 18O in CO2 with a reproducibility of better than δ18O= ± 0.3 oas determined from target gas measurements over a period of ten months. An Allan variance test shows that the δ18O repeatability reaches 0.1 ofor hourly means. The compatibility of the spectroscopic measurements was determined by comparing FTIR measurements of δ18O of ambient air to the mass-spectrometric measurements on flask samples episodically collected over two diurnal cycles (events). A compatibility of better than ± 0.1 ofor δ18O was found during these comparisons. Even though the FTIR precision does not reach that of isotope ratio mass spectrometry, a number of interesting scientific applications seem possible. In particular, investigation of processes that govern the δ18O variability of atmospheric CO2 on the regional scale seem very promising. Two episodes of recent ambient air measurements in Heidelberg, one in winter and one in summer, illustrate how high resolution regional δ18O and δ13C records may provide a better understanding of the regional scale processes leading atmospheric CO2 variability. However, quantitative analysis requires comprehensive knowledge on the isotopic signature of different CO2 sources and sinks as well as the influencing water reservoirs, which may largely govern the δ18O-CO2 variability during summer.