Diagenesis carbonate cement precipitation

Figure 7.42. Comparison between (A) an idealized plot of variation in 8180 and 813C for carbonates subjected to vadose and phreatic meteoric diagenesis (after Lohmann, 1988) with (B) the meteoric alteration trend observed for the Key Largo Limestone, Florida, U.S.A. (after Martin et al., 1986). The critical trend in isotopic composition is termed the meteoric calcite line. This trend may be modified at the water recharge surface where evaporation is an important process, caliche is formed and the diagenetic phases are depleted in 13C derived from soil-gas CO2. Another modification can occur distally to the recharge area where precipitating carbonate cements may have isotopic ratios nearly equivalent to dissolving phases.

Carbonate cements are often among the dominant components of diagenesis and hence are of decisive importance in determining the reservoir quality of sandstone sequences. Despite this, the timing, the geochemical conditions of precipitation and dissolution, as well as the source and fate of these cements are not fully understood. In continental and near-shore sediments, cements commonly precipitate as calcretes and dolocretes in the vadose and phreatic zones, and attain a variety of mineral-ogical, textural and distribution patterns as well as elemental and isotopic compositions. These cements form lenses and layers of densely cemented... 

One of the most important aspects of carbonate diagenesis is the net movement of carbonate minerals. This mass transfer can be accomplished on a small scale by diffusive transport or on a large scale by the flow of subsurface waters. It is the basic process by which secondary porosity is created and cementation occurs. In most cases, it involves carbonate mineral dissolution at one site and precipitation at another. While this can be simply accomplished where mineralogic transformations from a metastable phase to a more stable phase are involved, more complex mechanisms may be required within mineralogically homogeneous carbonate bodies. 

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