Abstract
Abstract. An African oxalogenic tree, the iroko tree (Milicia excelsa), has the property to enhance carbonate precipitation in tropical oxisols, where such accumulations are not expected due to the acidic conditions in these types of soils. This uncommon process is linked to the oxalate-carbonate pathway, which increases soil pH through oxalate oxidation. In order to investigate the oxalate-carbonate pathway in the iroko system, fluxes of matter have been identified, described, and evaluated from field to microscopic scales. In the first centimeters of the soil profile, decaying of the organic matter allows the release of whewellite crystals, mainly due to the action of termites and saprophytic fungi. In addition, a concomitant flux of carbonate formed in wood tissues contributes to the carbonate flux and is identified as a direct consequence of wood feeding by termites. Nevertheless, calcite biomineralization of the tree is not a consequence of in situ oxalate consumption, but rather related to the oxalate oxidation inside the upper part of the soil. The consequence of this oxidation is the presence of carbonate ions in the soil solution pumped through the roots, leading to preferential mineralization of the roots and the trunk base. An ideal scenario for the iroko biomineralization and soil carbonate accumulation starts with oxalatization: as the iroko tree grows, the organic matter flux to the soil constitutes the litter, and an oxalate pool is formed on the forest ground. Then, wood rotting agents (mainly termites, saprophytic fungi, and bacteria) release significant amounts of oxalate crystals from decaying plant tissues. In addition, some of these agents are themselves producers of oxalate (e.g. fungi). Both processes contribute to a soil pool of "available" oxalate crystals. Oxalate consumption by oxalotrophic bacteria can then start. Carbonate and calcium ions present in the soil solution represent the end products of the oxalate-carbonate pathway. The solution is pumped through the roots, leading to carbonate precipitation. The main pools of carbon are clearly identified as the organic matter (the tree and its organic products), the oxalate crystals, and the various carbonate features. A functional model based on field observations and diagenetic investigations with δ13C signatures of the various compartments involved in the local carbon cycle is proposed. It suggests that the iroko ecosystem can act as a long-term carbon sink, as long as the calcium source is related to non-carbonate rocks. Consequently, this carbon sink, driven by the oxalate carbonate pathway around an iroko tree, constitutes a true carbon trapping ecosystem as defined by ecological theory.
Highlights
Biomineralization in the Plant kingdom resulting in the presence of oxalate and/or carbonate crystals has been known for a long time (Leidy, 1883; Record, 1927; Campbell and Fisher, 1932; Harris 1933; Pobeguin, 1943, 1954; Carozzi, 1967; Franceschi and Horner, 1980)
Three types of biomineralization have been observed in the iroko tree (Milicia excelsa, Moraceae) among the numerous ones described in the natural environment: oxalatization, calcitization, and silicification (Braissant et al, 2004; Cailleau et al, 2005)
In an area originally expected to be carbonate-free near Daloa (Ivory Coast), calcium carbonate accumulations have been described in soils, as well as in iroko tree tissues
Summary
Biomineralization in the Plant kingdom resulting in the presence of oxalate and/or carbonate crystals has been known for a long time (Leidy, 1883; Record, 1927; Campbell and Fisher, 1932; Harris 1933; Pobeguin, 1943, 1954; Carozzi, 1967; Franceschi and Horner, 1980). Three types of biomineralization have been observed in the iroko tree (Milicia excelsa, Moraceae) among the numerous ones described in the natural environment: oxalatization, calcitization, and silicification (Braissant et al, 2004; Cailleau et al, 2005). In an area originally expected to be carbonate-free near Daloa (Ivory Coast), calcium carbonate accumulations have been described in soils ( originally acidic), as well as in iroko tree tissues. The photosynthetic process which leads to calcium oxalate accumulation in plant tissues has been well studied (Franceschi and Nakata, 2005). Cailleau et al.: Turning sunlight into stone: the oxalate-carbonate pathway
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