Northern Hemisphere atmospheric history of carbon monoxide since preindustrial times reconstructed from multiple Greenland ice cores
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Published:2022-04-01
Issue:3
Volume:18
Page:631-647
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ISSN:1814-9332
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Container-title:Climate of the Past
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language:en
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Short-container-title:Clim. Past
Author:
Faïn XavierORCID, Rhodes Rachael H.ORCID, Place Philip, Petrenko Vasilii V., Fourteau KévinORCID, Chellman Nathan, Crosier Edward, McConnell Joseph R.ORCID, Brook Edward J.ORCID, Blunier ThomasORCID, Legrand Michel, Chappellaz Jérôme
Abstract
Abstract. Carbon monoxide (CO) is a regulated pollutant and one of the key components
determining the oxidizing capacity of the atmosphere. Obtaining a reliable
record of atmospheric CO mixing ratios ([CO]) since preindustrial times is necessary
to evaluate climate–chemistry models under conditions different from today and to
constrain past CO sources. We present high-resolution measurements of CO
mixing ratios from ice cores drilled at five different sites on the Greenland
ice sheet that experience a range of snow accumulation rates, mean surface
temperatures, and different chemical compositions. An optical-feedback
cavity-enhanced absorption spectrometer (OF-CEAS) was coupled with continuous
melter systems and operated during four analytical campaigns conducted between
2013 and 2019. Overall, continuous flow analysis (CFA) of CO was carried out
on over 700 m of ice. The CFA-based CO measurements exhibit excellent
external precision (ranging from 3.3 to 6.6 ppbv, 1σ) and achieve
consistently low blanks (ranging from 4.1±1.2 to
12.6±4.4 ppbv), enabling paleoatmospheric
interpretations. However, the five CO records all exhibit variability that is too large
and rapid to reflect past atmospheric mixing ratio changes. Complementary
tests conducted on discrete ice samples demonstrate that these variations are
not artifacts of the analytical method (i.e., production of CO from organics
in the ice during melting) but are very likely related to in situ CO
production within the ice before analysis. Evaluation of the signal resolution and
co-investigation of high-resolution records of CO and total organic
carbon (TOC) suggest that past
atmospheric CO variations can be extracted from the records' baselines with
accumulation rates higher than 20 cm w.e.yr-1 (water equivalent per year). Consistent baseline CO records from four Greenland
sites are combined to produce a multisite average ice core reconstruction of
past atmospheric CO for the Northern Hemisphere high latitudes, covering the
period from 1700 to 1957 CE. Such a reconstruction should be taken as an upper
bound of past atmospheric CO abundance. From 1700 to 1875 CE, the record
reveals stable or slightly increasing values in the 100–115 ppbv
range. From 1875 to 1957 CE, the record indicates a monotonic increase from
114±4 to 147±6 ppbv. The ice core multisite CO
record exhibits an excellent overlap with the atmospheric CO record from
Greenland firn air which spans the 1950–2010 CE time period. The combined
ice core and firn air CO history, spanning 1700–2010 CE, provides useful
constraints for future model studies of atmospheric changes since the
preindustrial period.
Funder
Agence Nationale de la Recherche Seventh Framework Programme National Science Foundation Institut Polaire Français Paul Emile Victor
Publisher
Copernicus GmbH
Subject
Paleontology,Stratigraphy,Global and Planetary Change
Reference43 articles.
1. Allan, D.: Statistics of atomic frequency standards, P. IEEE, 54, 221–230, https://doi.org/10.1109/PROC.1966.4634, 1966. a 2. Butler, J. H., Battle, M. O., Bender, M., Montzka, S. A., Clarke, A. D., Saltzman, E. S., Sucher, C. M., Severinghaus, J. P., and Elkins, J. W.: A record of atmospheric halocarbons during the twentieth century from polar firn air, Nature, 399, 749–755, 1999. a 3. Clark, I. D., Henderson, L., Chappellaz, J., Fisher, D., Koerner, R., Worthy, D. E. J., Kotzer, T., Norman, A. L., and Barnola, J. M.: CO2 isotopes as tracers of firn air diffusion and age in an Arctic ice cap with summer melting, Devon Island, Canada, J. Geophys. Res.-Atmos., 112, D01301, https://doi.org/10.1029/2006jd007471, 2007. a 4. Collins, W. J., Lamarque, J.-F., Schulz, M., Boucher, O., Eyring, V., Hegglin, M. I., Maycock, A., Myhre, G., Prather, M., Shindell, D., and Smith, S. J.: AerChemMIP: quantifying the effects of chemistry and aerosols in CMIP6, Geosci. Model Dev., 10, 585–607, https://doi.org/10.5194/gmd-10-585-2017, 2017. a, b 5. Conte, L., Szopa, S., Séférian, R., and Bopp, L.: The oceanic cycle of carbon monoxide and its emissions to the atmosphere, Biogeosciences, 16, 881–902, https://doi.org/10.5194/bg-16-881-2019, 2019. a
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