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Weathering in a regolith on the Werenskioldbreen Glacier forefield (SW Spitsbergen). 2. Speciation of Fe, Mn, Pb, Cu and Zn in the chronosequence

Rzepa Grzegorz, Manecki Maciej, Jakubski Grzegorz, Kwaśniak-Kominek Monika, Czerny Jerzy, Górniak Dorota

Annales Societatis Geologorum Poloniae

2019

Vol. 89, No. 3

317--341

The evolution of chemical speciation of Fe, Mn, Pb, Cu, and Zn was investigated in the chronosequence of young sediments, exposed by a currently retreating Arctic glacier on Spitsbergen. Werenskioldbreen is a 27 km2 subpolar, land-terminated, polythermal glacier in recession, located near the SW coast of West Spitsbergen. Three samples of structureless till were collected at locations exposed for 5, 45 and 70 years. Four grain-size fractions were separated: > 63, 20–63, 2–20, and < 2 µm. Speciation of Fe, Mn, Pb, Cu, and Zn was determined using a 6-step sequential chemical extraction method: 1) 1 M sodium acetate, 2) 1 M hydroxylamine hydrochloride in acetic acid, 3) sodium dithionite in buffer, 4) acid ammonium oxalate, 5) boiling HCl, 6) residuum. The weathering in the proglacial area of the retreating glacier is very fast. The geochemical fates of the metals in question correlate with each other, reflecting a) the geochemical similarities between them, b) the similarities of their primary mineral sources, c) the significant role of incongruent dissolution. The weathering processes dominating the system are redox reactions and incongruent dissolution, followed by precipitation of secondary phases and partial sorption of aqueous species. As a result, the elements released from weathering minerals are only partially transported away from the system. The remaining part transforms by weathering from the coarse-grained fraction (dominated by fragments of primary minerals) into the fine-grained fraction (in the form of secondary, authigenic minerals or as species sorbed onto a mineral skeleton). This is very strongly pronounced within the chronosequence: the content of each of the metals studied correlates identically with the grain size, despite the differences in their chemical character and affinities. The microscope study presented herein indicates that the role of incongruent dissolution previously was underestimated. Also, the formation of coatings of secondary phases on primary mineral surfaces was observed. All these rapid weathering processes affect the mineral speciation of initial soils as well as the composition of mineral suspensions transported away by rivers to the nearby ocean.

Weathering in a regolith on the Werenskioldbreen forefield (SW Spitsbergen) : modelling of pore water chemistry

Kwaśniak-Kominek M., Manecki M., Rzepa G., Płonka A. M., Górniak D.

Annales Societatis Geologorum Poloniae

2016

Vol. 86, No. 3

249--264

The mineral framework and pore waters of glacial sediments exposed in the foreland of Weren- skioldbreen in SW Spitsbergen were sampled and analyzed to model the evolution of pore water chemistry, representing the advancement of weathering in a chronosequence. Three samples were taken at distances representing snapshots of approximately 5, 45 and 70 years of exposure. Complementary mineralogical analyses of the mineral framework and chemical analyses of pore waters, coupled with thermodynamic modelling of mineral-water interactions were applied. Recently uncovered sediments of the bottom moraine underwent very little weathering underneath the glacier cover; both the sediments and pore waters in the forefield of the Werenskioldbreen represent a very immature system. Poorly sorted sediments were deposited by the glacier and not reworked by fluvioglacial waters. The ratio of ‘amorphous iron’ to ‘free iron’ Feo/Fed increases with distance from the glacier terminus from 0.30 through 0.36 to 0.49, typical for fresh glacial till. The increase in saturation with CO2 (from p(CO2) –3.8 to –2.4) and the concentration of all major ions in pore waters (from 123 to 748 mg/L total dissolved solids, TDS) was observed in this young chronosequence. The waters evolved from carbonate- dominated to sulphate-dominated, indicating that with progress in weathering the dominating processes are equilibration with carbonates, oxidation of sulphides and the influence of gypsum precipitation by seasonal freeze-thaw cycles. Mass balance calculations and inverse modelling of the composition of pore waters, verified by microscopic observations of alteration on the surfaces of mineral grains, allowed thermodynamic confirmation of the fact that the relative significance of carbonate weathering decreases and that of sulphate increases down the chronosequence. The participation of silicate minerals in weathering is low, indicating a relatively immature stage of weathering within this particular chronosequence. It is significant that the morphology of etch pits and the formation of secondary phases apparent on mineral surfaces were identical, regardless of the distance from the glacier terminus. This might indicate that the mechanisms of particular weathering processes at the mineral-water interface are the same at the initial as well as at the more mature stages and do not change at least within ca. 70 years of exposure.