IRIS analyser assessment reveals sub-hourly variability of isotope ratios in carbon dioxide at Baring Head, New Zealand's atmospheric observatory in the Southern Ocean

Abstract

Abstract. We assess the performance of an isotope ratio infrared spectrometer (IRIS) to measure carbon (δ13C) and oxygen (δ18O) isotope ratios in atmospheric carbon dioxide (CO2) and report observations from a 26 d field deployment trial at Baring Head, New Zealand, NIWA's atmospheric observatory for Southern Ocean baseline air. Our study describes an operational method to improve the performance in comparison to previous publications on this analytical instrument. By using a calibration technique that reflected the principle of identical treatment of sample and reference gases, we achieved a reproducibility of 0.07 ‰ for δ13C-CO2 and 0.06 ‰ for δ18O-CO2 over multiple days. This performance is within the extended compatibility goal of 0.1 ‰ for both δ13C-CO2 and δ18O-CO2, which was recommended by the World Meteorological Organization (WMO). Further improvement in measurement performance is desirable to also meet the WMO network compatibility goals of 0.01 ‰ for δ13C-CO2 and 0.05 ‰ for δ18O-CO2, which is needed to resolve the small variability that is typical for background air observatories such as Baring Head. One objective of this study was to assess the capabilities and limitations of the IRIS analyser to resolve δ13C-CO2 and δ18O-CO2 variations under field conditions. Therefore, we selected multiple events within the 26 d record for Keeling plot analysis. This resolved the isotopic composition of endmembers with an uncertainty of ≤ 1 ‰ when the magnitude of CO2 signals is larger than 10 ppm. The uncertainty of the Keeling plot analysis strongly increased for smaller CO2 events (2–7 ppm), where the instrument performance is the limiting factor and may only allow for the distinction between very different endmembers, such as the role of terrestrial versus oceanic carbon cycle processes.