An improved method for atmospheric ¹⁴CO measurements

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.

An improved method for atmospheric ¹⁴CO measurements

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 liters 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, 1 σ). The method also for the first time includes accurate characterization of the overall procedural [14CO] blank associated with individual samples, 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 %, 1 σ) are achieved for samples that are directly accompanied by procedural blanks and whose mass is increased to ≈ 50 micrograms of carbon (µgC) prior to the 14C measurement via dilution with a high-CO, 14C-depleted gas.

The detection of solar proton produced ¹⁴CO

Major solar eruptions (coronal mass ejections) are accompanied by massive ejections of protons. When these charged particles head for the Earth through the interplanetary magnetic field with high flux and energy, a solar proton event (SPE) is recorded. Strong SPEs, in which energetic protons penetrate the atmosphere in large numbers are rare, but do have chemical effects (Crutzen, 1975; Jackman et al., 1990, 2001). They also have nucleonic effects by which they can almost instantaneously increase the atmospheric production of radio-nuclides, including 14C (radiocarbon), but this has never been demonstrated. We show, using satellite observations and modeling, that the 2nd most intensive set of SPEs on record, that of August-December 1989, must have caused detectable increases in atmospheric 14CO. This is confirmed by a sequence of peaks in the Baring Head (NZ) time series of 14CO observations (Brenninkmeijer, 1993), probably providing a unique indication of production of 14C by solar protons, thus demonstrating the use of SPE 14CO as an atmospheric tracer.

The detection of solar proton produced ¹⁴CO

Major solar eruptions (coronal mass ejections) are accompanied by massive ejections of protons. When these charged particles head for the Earth through the interplanetary magnetic field with high flux and energy, a solar proton event (SPE) is recorded. Strong SPEs, in which energetic protons penetrate the atmosphere in large numbers are rare, but do have chemical effects (Crutzen, 1975; Jackman et al., 1990, 2001). They also have nucleonic effects by which they can almost instantaneously increase the atmospheric production of radio-nuclides, including 14C (radiocarbon), but this has never been demonstrated. We show, using satellite observations and modeling, that the 2nd most intensive set of SPEs on record, that of August-December 1989, must have caused detectable increases in atmospheric 14CO. This is confirmed by a sequence of peaks in the Baring Head (NZ) time series of 14CO observations (Brenninkmeijer, 1993), providing a unique indication of production of 14C by solar protons, and demonstrating the use of SPE 14CO as an atmospheric tracer.