Poster, EGU General Assembly 2009, Vienna: 19.04.2009 - 24.04.2009
In our contribution we focus surface fluxes of the reactive trace gases NO, NO2, and O3 at the forest floor, using a flux gradient approach which specifically takes transportation times of the reactants into account. While in the first meter above the forest soil, vertical concentration gradients can be measured quite easily, the determination of vtr (the bulk (turbulent) transfer velocity; a measure for transport efficiency) requires unconventional approaches. We estimate vtr from measurements of a chemically inert tracer, namely the radioactive noble gas radon (Rn). The vertical distribution and the decay constant (0.0125 s-1) of the short-lived isotope 220Rn (t1/2= 55.6 s) are employed to calculate transportation times and corresponding bulk transfer velocities. Combined measurements of vertical concentration differences and soil surface fluxes by static chambers of the long-lived isotope 222Rn (t1/2= 3.81 d) result in bulk (turbulent) diffusion coefficients. Once the bulk turbulent diffusion coefficient (directly related to the bulk transfer velocity) for the near-surface gas transport at hand, it is applied to vertical concentration differences of NO, NO2, and O3 in order to infer corresponding surface fluxes. Results from these approaches obtained during field experiments in a Bavarian spruce forest at the Weidenbrunnen/ Fichtelgebirge (50.142°N 11.867°E, 780 m a.s.l.) in September 2007 and July 2008 are presented. Mean bulk transfer velocities in the first 30 centimetres of the trunk space ranged between 0.003 m s-1 and 0.016 m s-1, equivalent to bulk turbulent diffusion coefficients of 0.9 x 104 m2 s-1 up to 4.5 x 10-3 m2 s-1. We developed a numerical algorithm to consider fast (photo-)chemical reactions of the NO-NO2-O3 triad during the turbulent transport within the first meter about the forest floor. By this we corrected surface fluxes of NO, NO2 and O3 for the vertical flux divergence caused by chemical reactions. Finally, surface fluxes of NO, NO2 and O3 are compared to simultaneously performed direct surface flux measurements by dynamic soil chambers and eddy covariance techniques. Even under very stable meteorological conditions, when turbulence is so small (u* < 0.08 m s-1), that direct common methods (e.g. eddy covariance) are no longer applicable, the presented approaches can be used to characterise near-surface exchange of non-reactive and reactive trace gases.