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Banded iron formations (BIF), deposited prior to and concurrent with the Great Oxidation Event (GOE) at ~2.4 Ga, record changes in the oceanic and atmospheric chemistry during this critical time interval. Three previously unstudied drill-cores from the western Transvaal Basin, South Africa, capturing the rhythmically mesobanded Kuruman BIF and the overlying granular Griquatown BIF, were sampled every ~20 m. along core depth. These samples were analysed for mineralogy, geochemistry and bulk Fe and C-isotopes. Bulk Fe-isotopic values of 50 samples show an apparent relationship with mineralogy. The lower δ56Fe values (< -1.3) correlate with carbonate-rich samples, whereas higher δ56Fe values (>0.0) correspond to samples rich in bulk modal magnetite. To further investigate this relationship, a 3-step sequential extraction protocol was developed to separate the three main Fe-hosting fractions (Fe-carbonates, Fe-oxides and Fe-silicates). Rare Earth Element (REE) patterns were resolved for the individual fractions and using the leachate destruction protocol of Henkel et al. [1] we were able to measure for the first time species specific Fe-isotopes of bulk-BIF samples. Species specific Fe-isotopes are probably a better proxy for the Palaeoproterozoic ocean than bulk-rock values, since the latter are strongly influenced by the modal mineralogy of each sample. We used bulk-rock C-isotope data combined with the species specific REE and δ56Fe to argue that the Fe-carbonates (and possibly Fe-silicates) in the Transvaal BIFs record primary chemical signatures. It follows that chemical signatures can be preserved, through changes of the textural appearance of minerals in BIF during diagenesis and low-grade metamorphism [2]. Preliminary data indicate that the Fe-oxides (dominated by magnetite) are probably formed by recycling and mixing of precursor Fe-(oxy)hydroxides and ferrous sea- or pore-waters, since their positive δ56Fe values deviate strongly and consistently from the nega

Banded iron formations (BIF) deposited during the Great Oxidation Event (GOE) at ~2.4Ga, potentially capture chemical changes in the Paleoproterozoic atmosphere and ocean. The Kuruman and Griquatown BIFs in the Griqualand West Basin, South Africa were deposited concurrent with the GOE. Continuous drill-cores thereof provide important insights into the Paleoproterozoic environment. Bulk-rock samples of these cores show an apparent relationship between modal mineralogy and Fe-isotopes: low δ56Fe-values (<-1.3‰) correlate with samples rich in Fe-carbonate, whereas positive δ56Fe-values correspond to magnetite-rich samples. To interrogate this further, an existing sequential extraction scheme was modified to accommodate the BIF mineralogy [1]. Since ferric oxides are insignificant in the rocks we studied, the hydroxylamine and dithionite leaches could be omitted. The remaining extractions were optimized for the dissolution of three main Fe-hosting mineral fractions (Fe-carbonates, magnetite and Fe-silicates). The final silicate residue was dissolved in HF-HClO4-HNO3. The tests established a 3-step sequential extraction procedure to quantitatively separate the Fe-mineral fractions. To measure the species specific Fe-isotopes a processing-protocol was applied to break down the organic leachates [2]. Combining the species specific data (δ56Fe and REE) with bulk-rock data (C-isotopes and mineralogy) it becomes apparent that the BIFs have recorded primary signals from Paleoproterozoic seawater. References: [1] Poulton & Canfield (2005) Chem. Geo., 214, 209-221. [2] Henkel et al., (2016) Chemical Geology, 421, 93-102