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Plants fractionate Si isotopes which provides a useful Si tracer in the Si soil-plant cycle. This study reports plant Si content and Si-isotopic signatures in mature banana plants grown on soils with different weathering degree, but all developed from basaltic pyroclasts in the Mungo area, Cameroon. The delta Si-30 compositions were determined in various plant parts and soil surface horizons by MC-ICP-MS in dry plasma mode with external Mg doping to a precision of +/- 0.15aEuro degrees (+/- A 2 sigma(SD)). The Si-isotopic compositions in banana plants grown on weathered clayey soils (+0.54 +/- A 0.15aEuro degrees) are heavier than on weakly developed soils rich in fresh ash and pumice (+0.02 +/- A 0.15aEuro degrees). The corresponding bulk soils display lower delta Si-30 value in weathered soil (-1.41aEuro degrees) than in poorly developed soil (-0.41aEuro degrees). We suggest that the dissolved Si source for the plant, governed firstly by dissolution of easily weatherable minerals, was isotopically enriched in heavy isotopes through clay formation over long periods. At seasonal to annual time scale, this source is influenced by a combination of following processes: Si adsorption of light isotopes onto Fe oxides, plant Si uptake and recycling in surface horizons. This would provide an isotopically heavier Si source in the more weathered soil since the Fe oxides content increases with weathering. Plant Si-isotopic signature might thus reflect the soil weathering degree. This study further suggests that in addition to weathering processes, rivers isotopic signatures likely depend on the fate of phytoliths in the soil-plant-river system.

Variations of phytoplankton assemblages were studied in November–December 2001, in surface waters of the Southern Ocean along a transect between the Sub-Antarctic Zone (SAZ) and the Seasonal Ice Zone (SIZ; 46.9°–64.9°S; 142°–143°E; CLIVAR-SR3 cruise). Two regions had characteristic but different phytoplankton assemblages. Nanoflagellates( 20 μm), diatoms and dinoflagellates, were more abundant in the Antarctic Zone-South (AZ-S) and the SIZ, (60.9°–64.9°S). In AZ-S and SIZ diatoms ranged between 2.7 × 105 and 1.2 × 106 cells l−1, dinoflagellates from 3.1 × 104 to 1.02 × 105 cells l−1. A diatom bloom was in progress in the AZ-S showing a peak of 1.8 × 106 cells l−1. Diatoms were dominated by Pseudo-nitzschia spp., Fragilariopsis spp., and Chaetoceros spp. Pseudo-nitzschia spp. outnumbered other diatoms in the AZ-S. Fragilaropsis spp. were most numerous in the SIZ. Dinoflagellates contained autotrophs (e.g. Prorocentrum) and heterotrophs (Gyrodinium/Gymnodinium, Protoperidinium). Diatoms and dinoflagellates contributed most to the cellular carbon: 11–25 and 17–124 μg C l−1, respectively. Small cells dominated in the northern region characterized by the lowest N-uptake and new production of the transect. Larger diatom cells were prevalent in the southern area with higher values of N-uptake and new production. Diatom and nanoflagellate cellular carbon contents were highly correlated with one another, with primary production, and productivity related parameters. They contributed up to 75% to the total autotrophic C biomass. Diatom carbon content was significantly correlated to nitrate uptake and particle export, but not to ammonium uptake, while flagellate carbon was well correlated to ammonium uptake, but not to export. Diatoms have contributed highly to particle export along the latitudinal transect, while flagellates played a minor role in the export.

The determination of the plant-induced Si-isotopic fractionation is a promising tool to better quantify their role in the continental Si cycle. Si-isotopic signatures of the different banana plant parts and Si source were measured, providing the isotopic fractionation factor between plant and source. Banana plantlets (Musa acuminata Colla, cv Grande Naine) were grown in hydroponics at variable Si supplies (0.08, 0.42, 0.83 and 1.66 mM Si). Si-isotopic compositions were determined on a multicollector plasma source mass spectrometer (MC-ICP-MS) operating in dry plasma mode. Results are expressed as delta Si-29 relative to the NBS28 standard, with an average precision of +/- 0.08 parts per thousand (+/- 2 sigma(D)). The fractionation factor (29)epsilon between bulk banana plantlets and source solution is -0.40 +/- 0.11 parts per thousand. This confirms that plants fractionate Si isotopes by depleting the source solution in Si-28. The intra-plant fractionation Delta Si-29 between roots and shoots amounts to -0.21 +/- 0.08 parts per thousand. Si-isotopi c compositions of the various plant parts indicate that heavy isotopes discrimination occurs at three levels in the plant (at the root epidermis, for xylem loading and for xylem unloading). At each step, preferential crossing of light isotopes leaves a heavier solution, and produces a lighter solution. Si-isotopic fractionation processes are further discussed in relation with Si uptake and transport in plants. These findings have important implications on the study of continental Si cycle.