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Hydrology and Earth System Sciences An interactive open-access journal of the European Geosciences Union
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Volume 21, issue 12
Hydrol. Earth Syst. Sci., 21, 6363–6377, 2017
https://doi.org/10.5194/hess-21-6363-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 4.0 License.
Hydrol. Earth Syst. Sci., 21, 6363–6377, 2017
https://doi.org/10.5194/hess-21-6363-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 4.0 License.

Research article 15 Dec 2017

Research article | 15 Dec 2017

Non-destructive estimates of soil carbonic anhydrase activity and associated soil water oxygen isotope composition

Sam P. Jones, Jérôme Ogée, Joana Sauze, Steven Wohl, Noelia Saavedra, Noelia Fernández-Prado, Juliette Maire, Thomas Launois, Alexandre Bosc, and Lisa Wingate Sam P. Jones et al.
  • INRA, UMR ISPA, 33140, Villenave d'Ornon, France

Abstract. The contribution of photosynthesis and soil respiration to net land–atmosphere carbon dioxide (CO2) exchange can be estimated based on the differential influence of leaves and soils on budgets of the oxygen isotope composition (δ18O) of atmospheric CO2. To do so, the activity of carbonic anhydrases (CAs), a group of enzymes that catalyse the hydration of CO2 in soils and plants, needs to be understood. Measurements of soil CA activity typically involve the inversion of models describing the δ18O of CO2 fluxes to solve for the apparent, potentially catalysed, rate of CO2 hydration. This requires information about the δ18O of CO2 in isotopic equilibrium with soil water, typically obtained from destructive, depth-resolved sampling and extraction of soil water. In doing so, an assumption is made about the soil water pool that CO2 interacts with, which may bias estimates of CA activity if incorrect. Furthermore, this can represent a significant challenge in data collection given the potential for spatial and temporal variability in the δ18O of soil water and limited a priori information with respect to the appropriate sampling resolution and depth. We investigated whether we could circumvent this requirement by inferring the rate of CO2 hydration and the δ18O of soil water from the relationship between the δ18O of CO2 fluxes and the δ18O of CO2 at the soil surface measured at different ambient CO2 conditions. This approach was tested through laboratory incubations of air-dried soils that were re-wetted with three waters of different δ18O. Gas exchange measurements were made on these soils to estimate the rate of hydration and the δ18O of soil water, followed by soil water extraction to allow for comparison. Estimated rates of CO2 hydration were 6.8–14.6 times greater than the theoretical uncatalysed rate of hydration, indicating that CA were active in these soils. Importantly, these estimates were not significantly different among water treatments, suggesting that this represents a robust approach to assay the activity of CA in soil. As expected, estimates of the δ18O of the soil water that equilibrates with CO2 varied in response to alteration to the δ18O of soil water. However, these estimates were consistently more negative than the composition of the soil water extracted by cryogenic vacuum distillation at the end of the gas measurements with differences of up to −3.94 ‰ VSMOW–SLAP. These offsets suggest that, at least at lower water contents, CO2–H2O isotope equilibration primarily occurs with water pools that are bound to particle surfaces and are depleted in 18O compared to bulk soil water.

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