Abstract
Abstract. Carbon monoxide (CO) plays an important role in controlling the oxidizing
capacity of the atmosphere by reacting with OH radicals that affect
atmospheric methane (CH4) dynamics. We develop a process-based
biogeochemistry model to quantify the CO exchange between soils and the
atmosphere with a 5 min internal time step at the global scale. The model is
parameterized using the CO flux data from the field and laboratory
experiments for 11 representative ecosystem types. The model is then
extrapolated to global terrestrial ecosystems using monthly climate forcing
data. Global soil gross consumption, gross production, and net flux of the
atmospheric CO are estimated to be from −197 to −180, 34 to 36, and
−163 to −145 Tg CO yr−1 (1 Tg = 1012 g), respectively,
when the model is driven with satellite-based atmospheric CO concentration
data during 2000–2013. Tropical evergreen forest, savanna and deciduous
forest areas are the largest sinks at 123 Tg CO yr−1. The soil CO
gross consumption is sensitive to air temperature and atmospheric CO
concentration, while the gross production is sensitive to soil organic carbon
(SOC) stock and air temperature. By assuming that the spatially distributed
atmospheric CO concentrations (∼ 128 ppbv) are not changing over time,
the global mean CO net deposition velocity is estimated to be
0.16–0.19 mm s−1 during the 20th century. Under the future climate
scenarios, the CO deposition velocity will increase at a rate of
0.0002–0.0013 mm s−1 yr−1 during 2014–2100, reaching
0.20–0.30 mm s−1 by the end of the 21st century, primarily due to the
increasing temperature. Areas near the Equator, the eastern US, Europe and
eastern Asia will be the largest sinks due to optimum soil moisture and high
temperature. The annual global soil net flux of atmospheric CO is primarily
controlled by air temperature, soil temperature, SOC and atmospheric CO
concentrations, while its monthly variation is mainly determined by air
temperature, precipitation, soil temperature and soil moisture.
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