Warren W. Wood GSA Minneapolis, Mn Oct 11, 2011 MICHIGAN STATE UNIVERSITY Thomas F. Kraemer Thanks to Dave Clark USGS/NDC for logistical support in the.

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Presentation transcript:

Warren W. Wood GSA Minneapolis, Mn Oct 11, 2011 MICHIGAN STATE UNIVERSITY Thomas F. Kraemer Thanks to Dave Clark USGS/NDC for logistical support in the UAE

Dolomite is ubiquitous in the geologic record yet is apparently forming today only in limited environments, thus challenging the paradigm “The present is the key to the past”. The dolomite problem! Our thesis is that the dolomite problem is one of: Identifying on-going dolomitization Magnesium source and transport Viable geochemical conditions

234 U/ 238 U disequilibrium as indicator of recent dolomite precipitation Uranium in marine carbonate is released on carbonate dissolution. New mineral precipitation closes the system and restarts the 234 U/ 238 U “secular equilibrium clock” making possible to identify dolomite precipitation that has occurred less than ~ 10 6 years BP

Magnesium transport; The leaky aquifer ascending-brine model Traditional view of an aquifer system with intraformational flow. Solutes derived from weathering of aquifer A more realistic view of aquifer systems with solute leakage. Mg enters the aquifer from ascending geologic brines

Declining temperature plus mixing of ascending brines with intraformational flow, creates thermodynamic under saturation with respect to calcite and super saturation with respect to dolomite. Viable geochemical environment: Solute mixing and decreasing temperature Intraformational flow Temperature decease with ascent

Testing the hypothesis: UAE Location of study area

General location map Gachsaran Fm. UAE Groundwater flow lines and wells “x” sampled Current hydrology started about 7 x 10 6 years BP

Many of the uranium isotopes ( 234 U/ 238 U) from dolomite are out of equilibrium suggesting recent crystallization. It follows that dolomite is younger than ~ 10 6 years BP 234 U/ 238 U Uranium isotope ratio disequilibrium of dolomite

Magnesium mass balance Mass of magnesium entering control volume since start of flow system Q Dis = Q Rec + Q leak in – Q leak out CQ Dis = CQ Rec + CQ leak in - CO leak out ~11x10 9 kg Mass of magnesium present in a control volume of the aquifer M totMg = M dolMg + M liqMg ~ 6.8 x 10 8 kg 150 km 450 m1 m

Geothermal gradient ~ 3°C/100 m Pore water becomes thermodynamically under saturated with respect to calcite owing to calcite’s retrograde solubility. That is. the solutes are transported to areas of continuing lower temperatures along the vertical flow line and thus, remain undersaturated with respect to calcite. From Gumati, 1991 Geothermal gradient is ~ 2.7 °C per 100 m

 34 S in contemporary gypsum suggests source of ascending brines Modified from Paytan et.al., 2008 Pliocene Miocene Oligocene Eocene Paleoeocene 234 U/ 238 U is out of equilibrium in gypsum as well as dolomite suggesting contemporary gypsum precipitation. The  34 S values of 18.1 ‰ CDT suggests a Paleocene age brine consistent with ascending brine of that age.

Summary and conclusions Dolomite results from dissolving marine calcite by a combination of decreasing temperature and mixing with interformational waters and subsequent precipitation of dolomite. Ascending geologic brines provide the required magnesium for dolomite precipitation. Thank You!