Evaluating the performance of a Picarro G2207-i analyser for high-precision atmospheric O2 measurements
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Published:2023-01-24
Issue:2
Volume:16
Page:387-401
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ISSN:1867-8548
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Container-title:Atmospheric Measurement Techniques
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language:en
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Short-container-title:Atmos. Meas. Tech.
Author:
Fleming Leigh S.ORCID, Manning Andrew C.ORCID, Pickers Penelope A.ORCID, Forster Grant L.ORCID, Etchells Alex J.
Abstract
Abstract. Fluxes of oxygen (O2) and carbon dioxide (CO2) in and out of the
atmosphere are strongly coupled for terrestrial biospheric exchange
processes and fossil fuel combustion but are uncoupled for oceanic air–sea
gas exchange. High-precision measurements of both species can therefore
provide constraints on the carbon cycle and can be used to quantify fossil
fuel CO2 (ffCO2) emission estimates. In the case of O2,
however, due to its large atmospheric mole fraction (∼20.9 %) it is very challenging to measure small variations to the degree of
precision and accuracy required for these applications. We have tested an
atmospheric O2 analyser based on the principle of cavity ring-down
spectroscopy (Picarro Inc., model G2207-i), both in the laboratory and at the
Weybourne Atmospheric Observatory (WAO) field station in the UK, in
comparison to well-established, pre-existing atmospheric O2 and
CO2 measurement systems. In laboratory tests analysing dry air in high-pressure cylinders, we found
that the best precision was achieved with 30 min averaging and was
±0.5 ppm (∼±2.4 per meg). Also from continuous
measurements from a cylinder of dry air, we found the 24 h peak-to-peak
range of hourly averaged values to be 1.2 ppm (∼5.8 per meg).
These results are close to atmospheric O2 compatibility goals as set by
the UN World Meteorological Organization. However, from measurements of ambient
air conducted at WAO we found that the built-in water correction of the
G2207-i does not sufficiently correct for the influence of water vapour on
the O2 mole fraction. When sample air was dried and a 5-hourly baseline
correction with a reference gas cylinder was employed, the G2207-i's results
showed an average difference from the established O2 analyser of 13.6±7.5 per meg (over 2 weeks of continuous measurements). Over the
same period, based on measurements of a so-called “target tank”, analysed
for 12 min every 7 h, we calculated a repeatability of ±5.7±5.6 per meg and a compatibility of ±10.0±6.7 per meg
for the G2207-i. To further examine the G2207-i's performance in real-world
applications we used ambient air measurements of O2 together with
concurrent CO2 measurements to calculate ffCO2. Due to the
imprecision of the G2207-i, the ffCO2 calculated showed large
differences from that calculated from the established measurement system
and had a large uncertainty of ±13.0 ppm, which was roughly double
that from the established system (±5.8 ppm).
Funder
Natural Environment Research Council
Publisher
Copernicus GmbH
Subject
Atmospheric Science
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