T238 Marine Redox Evolution: Controls and Consequences I
Wednesday, 3 November 2010
8:00 AM - 12:00 PM
Room 203
SULFUR ISOTOPE SYSTEMATICS IN A LOW SULFATE, PERMANENTLY ANOXIC LAKE
Paper number: T238-5
Program: Technical Sessions
Time: 9:05 AM – 9:20 AM
Authors
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Matthew T. HurtgenNorthwestern University, Evanston, IL
Abstract
Surface water sulfate concentrations were ~275mM but dropped sharply below the chemocline (11.5m) to ~125mM as bacterial sulfate reduction occurred within the anoxic bottom waters. d34Ssulfate values above the chemocline were relatively constant with depth (~5‰), but increase dramatically in the lower 4 meters of anoxic bottom waters. The sulfur isotope composition of the sulfide buried below the anoxic water column approached the sulfur isotope composition of the surface water sulfate resulting in a small D34Ssulfate-sulfide value (~5‰). By contrast, the sulfur isotope composition of pyrite buried at the relatively shallow, oxic site was 34S-depleted relative to the anoxic site resulting in a larger D34Ssulfate-sulfide value (~11‰). This preliminary work highlights the relationship among d34Ssulfate, d34Ssulfide, and water column depth within an anoxic, low-sulfate system and the importance of understanding how the sulfate reservoir evolves within a spatial context and the implications for the sulfur isotope composition of pyrite that is ultimately buried in these systems.