scholarly journals Supplementary material to "Impact of atomic chlorine on the modelling of total methane and its <sup>13</sup>C : <sup>12</sup>C isotopic ratio at global scale"

Author(s):  
Joël Thanwerdas ◽  
Marielle Saunois ◽  
Antoine Berchet ◽  
Isabelle Pison ◽  
Didier Hauglustaine ◽  
...  
Author(s):  
Hylke E. Beck ◽  
Noemi Vergopolan ◽  
Ming Pan ◽  
Vincenzo Levizzani ◽  
Albert I. J. M. van Dijk ◽  
...  

2021 ◽  
Author(s):  
Frerk Pöppelmeier ◽  
David J. Janssen ◽  
Samuel L. Jaccard ◽  
Thomas F. Stocker

2019 ◽  
Author(s):  
Antoine Berchet ◽  
Isabelle Pison ◽  
Patrick M. Crill ◽  
Brett Thornton ◽  
Philippe Bousquet ◽  
...  

2006 ◽  
Vol 6 (6) ◽  
pp. 1611-1625 ◽  
Author(s):  
T. S. Rhee ◽  
C. A. M. Brenninkmeijer ◽  
T. Röckmann

Abstract. The removal of molecular hydrogen (H2) from the atmosphere is dominated by the uptake in soils. Notwithstanding, estimates of the magnitude of this important process on a global scale are highly uncertain. The CARIBIC aircraft observations of the seasonal variations of H2 and its D/H isotopic ratio in the Northern Hemisphere allow an independent, better constrained estimate. We derive that 82% of the annual turnover of tropospheric H2 is due to soil uptake, equaling 88 (±11)Tg a-1, of which the Northern Hemisphere alone accounts for 62 (±10)Tg a-1. Our calculations further show that tropospheric H2 has a lifetime of only 1.4 (±0.2) years – significantly shorter than the recent estimate of ~2 years – which is expected to decrease in the future. In addition, our independent top-down approach, confined by the global and hemispheric sinks of H2, indicates 64 (±12)Tg a-1 emissions from various sources of volatile organic compounds by photochemical oxidation in the atmosphere. This estimate is as much as up to 60% larger than the previous estimates. This large airborne production of H2 helps to explain the fairly homogeneous distribution of H2 in the troposphere.


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