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Tectonic control of bioalteration in modern and ancient oceanic crust as evidenced by carbon isotopes
Author(s) -
Furnes Harald,
Dilek Yildirim,
Muehlenbachs Karlis,
Banerjee Neil R.
Publication year - 2006
Publication title -
island arc
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.554
H-Index - 58
eISSN - 1440-1738
pISSN - 1038-4871
DOI - 10.1111/j.1440-1738.2006.00516.x
Subject(s) - geology , oceanic crust , crust , pillow lava , ophiolite , seafloor spreading , isotopes of carbon , rift , geochemistry , basalt , carbonate , tectonics , total organic carbon , lava , paleontology , subduction , volcano , chemistry , environmental chemistry , organic chemistry
We review the carbon‐isotope data for finely disseminated carbonates from bioaltered, glassy pillow rims of basaltic lava flows from in situ slow‐ and intermediate‐spreading oceanic crust of the central Atlantic Ocean (CAO) and the Costa Rica Rift (CRR). The δ 13 C values of the bioaltered glassy samples from the CAO show a large range, between −17 and +3‰ (Vienna Peedee belemnite standard), whereas those from the CRR define a much narrower range, between −17‰ and −7‰. This variation can be interpreted as the product of different microbial metabolisms during microbial alteration of the glass. In the present study, the generally low δ 13 C values (less than −7‰) are attributed to carbonate precipitated from microbially produced CO 2 during oxidation of organic matter. Positive δ 13 C values >0‰ likely result from lithotrophic utilization of CO 2 by methanogenic Archaea that produce CH 4 from H 2 and CO 2 . High production of H 2 at the slow‐spreading CAO crust may be a consequence of fault‐bounded, high‐level serpentinized peridotites near or on the sea floor, in contrast to the CRR crust, which exhibits a layer‐cake pseudostratigraphy with much less faulting and supposedly less H 2 production. A comparison of the δ 13 C data from glassy pillow margins in two ophiolites interpreted to have formed at different spreading rates supports this interpretation. The Jurassic Mirdita ophiolite complex in Albania shows a structural architecture similar to that of the slow‐spreading CAO crust, with a similar range in δ 13 C values of biogenic carbonates. The Late Ordvician Solund–Stavfjord ophiolite complex in western Norway exhibits structural and geochemical evidence for evolution at an intermediate‐spreading mid‐ocean ridge and displays δ 13 C signatures in biogenic carbonates similar to those of the CRR. Based on the results of this comparative study, it is tentatively concluded that the spreading rate‐dependent tectonic evolution of oceanic lithosphere has a significant control on the evolution of microbial life and hence on the δ 13 C biosignatures preserved in disseminated biogenic carbonates in glassy, bioaltered lavas.