biomarkers in Archaean banded iron formations from Pilbara and Dhawar Craton
2006
The origin of Archeaen banded iron formations (BIF) and the role of biosphere in Fe
precipitation is still highly debated. In order to elucidate these processes, detailed
mineralogical and textural analyses combined with δ15N, δ56Fe and δ13C data were obtained
on Fe-oxide bands from Marble Bar chert Unit (MB, 3.46 Ga, Pilbara craton, W. Australia)
and a BIF from the Bababudan Group (BG, 2.7-2.9 Ga, Dhawar Craton, Southern India).
Both samples are composed of alternating quartz and Fe-oxide bands with wavy microtextures.
CI- normalized REE patterns show that MB reflects hydrothermal fluid/basalt
interactions, while BG precipitated from a hydrothermal fluid/seawater mixture. In MB,
nano-cristalline hematite replaced magnetite, Mg-calcite and Fe-sulfides producing a
matlike surface, preserving nanometric N-bearing amorphous carbon nodules. Measured
C/N ratios (2.3 to 52) are typical of Precambrian organic matter. The δ56Fe of -0.40±0.02‰
suggests MOR-hydrothermal fluids as a Fe-source, while a δ15N of +7.4±0.4‰ is
compatible with nitrification-denitrification processes. BG is composed of intergrown
magnetite and hematite. Disseminated grunerite and magnetite grew during low T
metamorphism. Fe-oxide spherules compose vermicular-filaments that nucleated
perpendicular to quartz surfaces. Fe-oxide spherule bunches are perfectly preserved in the
silica bands forming micrometric mats, which contain heterogeneously distributed N
(~0.09at.%) and C (0.51 at.%, C/N=5.73). Bulk δ13C of -15.35‰±0.10 points to an organic
origin for C. The δ56Fe in Fe and Si layers (0.75‰ to 2.16‰) is compatible with a
chemical precipitation for BIF. A negative correlation between δ56Fe and the Th/U ratio
suggests that Fe isotopic variations are related to fluid circulation and re-precipitation of
Fe-oxides. High δ15N, on one Fe-oxide layer, of +21.8±0.7‰, corresponds to that observed
for Archeaen BIFs and may be related to nitrate-dependent microbial oxidation of Fe.
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