Abstract
Abstract. The global tropospheric distribution of molecular hydrogen (H2) and its uptake by the soil are simulated using a model called CHemical AGCM (atmospheric general circulation model) for the Study of the Environment and Radiative forcing (CHASER), which incorporates a two-layered soil diffusion/uptake process component. The simulated distribution of deposition velocity over land is influenced by regional climate, and has a global average of 3.3×10−2 cm s−1. In the region north of 30° N, the amount of soil uptake shows a large seasonal variation corresponding to change in biological activity due to soil temperature and change in diffusion suppression by snow cover. In the temperate and humid regions in the mid- to low- latitudes, the uptake is mostly influenced by the soil air ratio, which controls the gas diffusivity in the soil. In the semi-arid regions, water stress and high temperatures contribute to the reduction of biological activity, as well as to the seasonal variation in the deposition velocity. A comparison with the observations shows that the model reproduces both the distribution and seasonal variation of H2 relatively well. The global burden and tropospheric lifetime of H2 are 150 Tg and 2.0 yr, respectively. The seasonal variation in H2 mixing ratios at the northern high latitudes is mainly controlled by a large seasonal change in the soil uptake. In the Southern Hemisphere, seasonal change in net chemical production and inter-hemispheric transport are the dominant causes of the seasonal cycle, while large biomass burning contributes significantly to the seasonal variation in the tropics and subtropics. Both observations and the model show large inter-annual variations, especially for the period 1997–1998, associated with large biomass burning in the tropics and at Northern Hemisphere high latitudes. The soil uptake shows relatively small inter-annual variability compared with the biomass burning signal. Given that the thickness of biologically inactive layer plays an important role in the soil uptake of H2, its value in the model is chosen to achieve agreement with the observed H2 trends. Uncertainty of the estimated soil uptake flux in the semi-arid region is still large, reflecting the discrepancy in the observed and modeled seasonal variations.
Highlights
In the troposphere, molecular hydrogen (H2) has an average mixing ratio of ∼530 ppb, the second highest after methane (CH4, ∼1750 ppb) among the reactive tracers
The enzyme activity is still maintained near freezing point, biological activity in areas like Siberia stops when the soil temperature falls below −25 ◦C; this is due to a significant reduction in the enzyme activity caused by the freezing of soil moisture
The variation in soil diffusivity and biological activity in the soil are calculated as a function of soil temperature and moisture, which are calculated as prognostic variables in the land process module of the model
Summary
Molecular hydrogen (H2) has an average mixing ratio of ∼530 ppb (parts per billion), the second highest after methane (CH4, ∼1750 ppb) among the reactive tracers. Hauglustaine and Ehhalt (2002) used a chemical transport model to show good agreement between the observed and simulated H2 mixing ratio in the Southern Hemisphere and the tropics, but reported an overestimation of the seasonal maximum in the Northern Hemisphere. This may have resulted from their estimation of the soil uptake flux derived from net primary productivity (NPP). We used a global chemistry transport model combined with a land process model that included explicitly the soil uptake processes, to calculate the surface deposition flux and the concentration of H2, and discuss the spatial and temporal variations and the global budget of H2 in the troposphere
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