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            Chapter 10


            PORE  WATER  COMPACTION  CHEMISTRY  AS  RELATED  TO
            OVERPRESSURES

            H.H. RIEKE, G.V. CHILINGAR and J.O. ROBERTSON JR.




            INTRODUCTION
               Much  has  been  written  in  the  petroleum  geology  literature  on  the  geochemical
            evolution  of  pore  liquids  and  gases  associated  with  fluid  flow  systems  in  recent
            and  ancient  sedimentary  basins.  The  dialogues  include  observations  about  the  origin
            of  interstitial  fluids,  measurements  of  the  active  chemical  diagenetic  processes,  and
            resulting mass-transport properties,  which arise during the  development of sedimentary
            basins. Effects of thermal and chemical factors and the dynamic transfer of fluids within
            the basins leave imprints on the pore-fluid chemistry and generation of abnormally high
            (AHFP) or abnormally low formation pressures  (ALFP).
               It  is  the  purpose  of  this  chapter to  present  and  validate  a  hypothetical  model  that
            explains  the  differences  between  the  salinities  of pore  water  in  sandstones  and  shales
            in  the  gravitationally  compacted  sedimentary  basins  of  Tertiary  age.  The  explanation
            presented here is based on two diverse, relative scales of resolution-  microscopic (10 -2
            to  10 -4 m) and gigascopic (> 105 m). The gigascopic scale presents  evidence from field
            observations,  whereas  the  microscopic  scale  focuses  on  laboratory  experiments  that
            dealt  with  the  chemistry  of  fluids  in  the  pore  space.  Mathematical  and  conceptual
            models  are presented and discussed,  which support these observations.  Additionally, the
            relevance of the isotopic character of shale pore water is evaluated for this environment.
            The all-inclusive premise is that the pore-water salinities in  shales  are lower than those
            in associated sandstones  in compacting  sedimentary basins.  A  corollary to  our premise
            is that the salinities of solutions  'squeezed out'  during  compaction are a function of the
            overburden  pressure,  temperature,  and  rate  of  compaction.  The  salinities  of  solutions
            expelled out of pelitic sediments decrease with increasing depth in young basins having
            a  high  sedimentation  rate  and,  therefore,  a  high  sediment  compaction  rate.  In  basins
            with low sedimentation rates, the compaction rates are low and the pore-water salinities
            increase with increasing depth.  AHFP zones are normally absent in these basins.
               A  majority  of previous  investigations  focused  on placing  the  observed  single-phase
            fluid  flow  systems  and  their  geological  outcomes  into  four  general  categories:  after
            sedimentation, during burial, during tectonic deformation,  and during uplift and erosion.
            These four  categories  define  the  accepted,  customary  steps  in  sedimentary basin  filling
            and evolution.
               The following references on pore-fluid chemistry and fluid flow provide a background
            to  the  above  four  categories.  Goldberg  et  al.  (1971),  Manheim  (1976),  Sayles  (1979),
            and  Gieskes  et  al.  (1990)  presented  chemical  analysis  of  sea,  bottom,  and  pore  waters
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