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62                         TEMPERATURE AND PRESSURE IN THE SUBSURFACE

           by the geothermal gradient. Inasmuch as the desorbed (interlayer) water is added to
           the interstitial water, abnormally high pore pressures may develop if the water
           cannot escape. Under some conditions, the rising pore pressure in shales may reduce
           the montmorillonite dehydration rate and release of water. The result will be similar
           to that arising from a low geothermal gradient, i.e., reduction in the rate of illite
           formation. Under favorable conditions, the illite may be hydrated, which is
           accompanied by a release of heat and its transformation to secondary montmor-
           illonite. The relative intensity of dehydration (illite formation) and the illite
           hydration (formation of secondary montmorillonite) may determine the pore
           pressure.
             The sedimentation rate and the sediment sources do not remain constant
           with time. Thus, different zones may differ in the dehydration rate because of
           changes in the sedimentation rate or type of sedimentary material. Transitions from a
           zone with normal pressures and normal dehydration rate to an AHFP zone may
           indicate either the effect of diagenetic and catagenetic processes or a lag in the
           development of these processes. The montmorillonite content may remain the same
           or even increase with depth. This, however, does not mean that the process
           of dehydration of montmorillonite to illite is replaced by the illite hydration, although
           this is possible. Instead, it could mean that dehydration process in the AHFP zones is
           slow; therefore, these zones may be characterized by higher (or equal) montmor-
           illonite contents than those in the younger zones with normal shale pore pressure.



           3.2.5. Effect of formation water chemistry

             The formation water chemistry has a significant influence on the intensity of
           postsedimentary transformations. Thus, it is important to ascertain the nature of
           hydrochemical scenario observed in the Cenozoic sequence of the South Caspian
           Basin, namely: whether it is a consequence of diagenetic and catagenetic processes in
           shales and the transformation of clay minerals, or it is formed predominantly as a
           result of the action of other factors (e.g., compaction). In this connection, the
           problem presenting the greatest interest is the origin of inverted hydrochemical
           profile in the section of the South Caspian Basin, i.e., with depth, calcium chloride
           waters are replaced by less saline sodium bicarbonate waters. The writers obtained
           numerous data from the laboratory analyses and field observations, indicating a
           decrease in the salinity of pore waters in sands with depth. Replacement of calcium
           chloride water by alkaline sodium bicarbonate water is characteristic for the AHFP
           zones in the South Caspian Basin areas (Buryakovsky, 1974). Analogous data on the
           decrease of formation water salinity with increasing pressure were also noted in the
           Gulf of Mexico (Fertl, 1976).
             The appearance of hydrochemical inversion in the stratigraphic section of
           the South Caspian Basin may be explained by the genetic relationship between
           the hydrochemical environment and the development of abnormally high pore
           pressures in shales. The water of primarily sodium bicarbonate type characterizes the
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