Atmospheric Measurement Techniques (Mar 2021)

An improved method for atmospheric <sup>14</sup>CO measurements

  • V. V. Petrenko,
  • A. M. Smith,
  • E. M. Crosier,
  • R. Kazemi,
  • P. Place,
  • A. Colton,
  • B. Yang,
  • Q. Hua,
  • L. T. Murray

DOI
https://doi.org/10.5194/amt-14-2055-2021
Journal volume & issue
Vol. 14
pp. 2055 – 2063

Abstract

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Important uncertainties remain in our understanding of the spatial and temporal variability of atmospheric hydroxyl radical concentration ([OH]). Carbon-14-containing carbon monoxide (14CO) is a useful tracer that can help in the characterization of [OH] variability. Prior measurements of atmospheric 14CO concentration ([14CO] are limited in both their spatial and temporal extent, partly due to the very large air sample volumes that have been required for measurements (500–1000 L at standard temperature and pressure, L STP) and the difficulty and expense associated with the collection, shipment, and processing of such samples. Here we present a new method that reduces the air sample volume requirement to ≈90 L STP while allowing for [14CO] measurement uncertainties that are on par with or better than prior work (≈3 % or better, 1σ). The method also for the first time includes accurate characterization of the overall procedural [14CO] blank associated with individual samples, which is a key improvement over prior atmospheric 14CO work. The method was used to make measurements of [14CO] at the NOAA Mauna Loa Observatory, Hawaii, USA, between November 2017 and November 2018. The measurements show the expected [14CO] seasonal cycle (lowest in summer) and are in good agreement with prior [14CO] results from another low-latitude site in the Northern Hemisphere. The lowest overall [14CO] uncertainties (2.1 %, 1σ) are achieved for samples that are directly accompanied by procedural blanks and whose mass is increased to ≈50 µgC (micrograms of carbon) prior to the 14C measurement via dilution with a high-CO 14C-depleted gas.