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American Journal of Science, Vol. 308, September 2008, P.851-884; doi:10.2475/07.2008.03

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Formation of replacement dolomite in the Latemar carbonate buildup, Dolomites, northern Italy: Part 1. Field relations, mineralogy, and geochemistry

Sarah K. Carmichael*, John M. Ferry**,{dagger} and William F. McDonough***

* Department of Geology, Appalachian State University, Boone, North Carolina 28608, USA
** Department of Earth and Planetary Sciences, Johns Hopkins University, Baltimore, Maryland 21218, USA
*** Department of Geology, University of Maryland, College Park, Maryland 20742, USA

{dagger} Corresponding author: jferry{at}jhu.edu

Replacement dolomite in the Latemar carbonate buildup, northern Italy, formed when limestone was infiltrated by and reacted with Mg-rich fluid. It occurs in discrete bodies in sharp contact with unreacted limestone. The dolomite developed in a nearly orthogonal lattice of vertical columns (replacement of limestone breccia pipes) and sheets (replacement along fractures and limestone-dike contacts) and of nearly horizontal bedding-parallel sheets and tubes. Mapped patterns of replacement dolomite directly image that part of the plumbing system in which the amount of fluid flow was sufficient to form dolomite. Decreases in the proportion of dolomite relative to limestone and in the proportion of vertical relative to horizontal dolomite-limestone contacts with increasing elevation indicate that the overall direction of fluid flow was upward and then outward along more permeable bedding horizons. Dolomite is significantly enriched in Fe, Mn, and Zn, as well as in Mg, relative to calcite in precursor limestone but not in Cu, Ni, Co, Cr, Ba, or Pb. The Fe, Mn, and Zn content of dolomite varies spatially within outcrops from the scale of meters down to the micron scale of oscillatory growth zoning in individual dolomite crystals. The variation is interpreted in terms of a dolomitizing fluid that, unlike unmodified seawater, contained significant amounts of Fe, Mn, and Zn, as well as of Mg, and whose composition varied in space at a range of scales and in time at the site of growth of individual dolomite crystals. A nearly complete overlap in the {delta}13C of dolomite (2.0–4.6{per thousand}, VPDB) and calcite (1.1–4.0{per thousand}) is evidence that the {delta}13C of most dolomite was inherited directly from the calcite precursor. Measured {delta}18O of dolomite has a wide range (21.8–27.7{per thousand}, VSMOW) overlapping with that of calcite (23.4–28.5{per thousand}) but shifted to lower values. Dolomite with {delta}18O <23.4 permil could not have been equilibrium with any analyzed calcite at any temperature. The ranges in {delta}18ODol and {delta}18OCal and values of {delta}18ODol <23.4 permil both indicate that {delta}18O of calcite and dolomite were set by oxygen isotope exchange with the same fluid over a range of temperatures, with isotopically different fluids, or both.




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S. K. Carmichael and J. M. Ferry
Formation of replacement dolomite in the Latemar carbonate buildup, Dolomites, northern Italy: Part 2. Origin of the dolomitizing fluid and the amount and duration of fluid flow
Am J Sci, October 1, 2008; 308(8): 885 - 904.
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