2007 GSA Denver Annual Meeting (28–31 October 2007)

Paper No. 2
Presentation Time: 8:15 AM

OCEANIC STRATIFICATION AND MIXING IN THE AFTERMATH OF A NEOPROTEROZOIC GLACIATION: CARBON AND SULFUR ISOTOPE EVIDENCE FROM THE ZHAMOKETI CAP DOLOSTONE IN NORTHWEST CHINA


SHEN, Bing, Department of Geosciences, Virginia Polytechnic Institute and State Univ, Blacksburg, VA 24061, XIAO, Shuhai, Department of Geosciences, Virginia Polytechnic Institute and State University, 4044 Derring Hall, Blacksburg, VA 24061, KAUFMAN, Alan J., Geology Department, University of Maryland, College Park, MD 20742, BAO, Huiming, Department of Geology and Geophysics, Louisiana State Univ, Baton Rouge, LA 70803, ZHOU, Chuanming, Nanjing Institute of Geology and Paleontology, Chinese Academy of Sciences, Nanjing, 210008, China and WANG, Haifeng, Nanjing Institute of Geology and Palaeontology, Nanjing, 210008, China, bingshen@vt.edu

The Tereeken diamictite and overlying Zhamoketi cap dolostone in the Quruqtagh area, eastern Chinese Tianshan of northwest China, represent a diamictite-carbonate pair deposited in the aftermath of a Neoproterozoic ice age (<727 but >615 Ma) possibly equivalent to the Marinoan glaciation. We analyzed stable isotopes (δ13C, δ18O, δ34S) and elemental concentrations (Ca, Mg, S, Sr, Fe, and Mn) of the ~10-m-thick Zhamoketi cap dolostone. The δ13C values reveals that organic and carbonate carbon isotope compositions are relatively stable, averaging at –28.2‰ and –4.6‰, respectively. The lower 2.5 m is characterized by high abundances of CAS (carbonate associated sulfate) with δ34SCAS compositions varying between +9‰ and +15‰. In the overlying interval, CAS abundance decreases rapidly while δ34SCAS values raise ~5‰ within an interval of peloidal dolomicrosparite. Sulfur isotopic compositions of pyrite extracted from the cap dolostone are largely indistinguishable from those of CAS, but direct comparison shows that pyrite is typically enriched in 34S relative to trace sulfate. Hypotheses to explain the observations must account for both the highly positive δ34S for pyrites and the apparent inverse sulfur isotope fractionation between sulfate and sulfide. We propose that CAS and pyrite were derived from two isotopically distinct reservoirs in a chemically stratified basin. In this model, CAS was derived from shallow, oxidized surface waters with moderate sulfate concentration and depleted in 34S due to the post-glacial influx of sulfur from continent weathering. In contrast, sulfate available for the formation of pyrite (either in pore fluids or the water column) was derived from anoxic bottom water with low sulfate concentration and enriched in δ34S due to long-term bacterial sulfate reduction during the ice age. The rapid shift in CAS abundance and sulfur isotope compositions within the cap dolostone is interpreted to reflect the mixing of deep and shallow water reservoirs.