Page 216 - Geochemistry of Oil Field Waters
P. 216

SEDIMENTARY ROCKS                                                    203


            Depositional  environments of evaporites

              Calcium carbonate precipitates  from sea water after it begins to evaporate
            (Usiglio, 1849). Removal of  calcium ions from solution increases the Mg/Ca
            ratio in the residual brine, and the precipitated calcium carbonate reacts with
            the magnesium enriched brine to form dolomite (Deffeyes et al., 1964). The
            common order of  evaporite deposition in a basin cut off from the open sea is
            limestone > dolomite > gypsum > halite > potash. Evaporite deposition can
            be stopped in a basin by a change in climatic regimen or tectonism. If  it were
            changed  and  new  water  were  allowed  to enter, the already deposited salts
            probably  would  be  effectively  protected  by the superadjacent high-density
            brine, and the lighter waters either meteoric or sea water would float on top,
            developing euxinic conditions similar to a situation found in the Black Sea.
              Toxic  conditions  in  euxinic  areas  tend  to  preserve  deposited  organic
            matter. The preserved organic  matter later can be transformed  to hydrocar-
            bons  and  petroleum.  Hypersaline  lagoons  often  are  very  prolific  in  the
            production of  organic matter (Phleger and Ewing, 1962). Algal pads and an
            abundance of  organic organisms are characteristic of a high-pH, high-salinity
            environment  (Carpelan,  1957)  such  as  exists  before  euxinic  conditions
            develop.
              The  deposition  of  evaporites  occurs  when  water  evaporates  under  re-
            stricted  environmental  conditions.  The  restrictions  usually  are  caused  by
            tectonism  such as an uplift, regression of  the strand line leaving a relict sea,
            or biological building of a reef.
              Sloss  (1953) outlined  five environments  from  which  evaporites deposit;
            they are normal  marine,  euxinic, penesaline, saline, and supersaline. Primary
            carbonates  and  dolomitized carbonates precipitate from the normal marine
            environment where the water contains about 35,000 mg/l of dissolved solids.
            Limestones  rich  in  organic  matter  and  black  shales  often  are  related  to
            euxinic environments.
              In  the  penesaline  environment  carbonates and  primary  dolomite  form.
           The salinity of  the water is toxic to normal  marine  life but not sufficiently
           saline so that halite precipitates. The dissolved solids in the water range from
           about 250,000 mg/l to 350,QOO mg/l.
              From  a  saline  environment  carbonates,  sulfates,  and halites will precipi-
           tate.  From a supersaline environment potassium compounds will precipitate,
           and  the amount  of  dissolved solids  in  the solution  will  be about 500,000
           mg/l.
              A  simplistic  model  of  an  evaporite  basin is a closed basin initially filled
           with sea water and evaporated to dryness.  In the isochemical system a layer
           of  calcium carbonate is deposited  over the entire basin floor as evaporation
           proceeds.  Next, gypsum is deposited and when the water is reduced to about
            10% of the original volume, halite precipitates. Halite will deposit only in the
           deeper parts of the basin and if  the solution goes to dryness the more soluble
           salts will deposit in any remaining depressions and on top of the halite.
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