Page 17 - Carbonate Facies in Geologic History
P. 17

4                                       Principles of Carbonate Sedimentation

                  It is  noteworthy that  most  major deposits  of limestone  or  dolomite are  re-
               markably pure carbonate and contain only a few  percent of argillaceous or silty
               insoluble material. Such "contaminants" are obviously detrimental to deposition
               of calcareous sediment.
                  Two other processes are important,  though  probably not necessary for  car-
               bonate deposition: agitation of water and strong evaporation. The former process
               is discussed later. The role of evaporation in concentrating sea water in basins or
               on  tidal flats  is  well  established.  Biochemical  or wholely  inorganic  removal  of
               CaC0 3  from  sea water must  occur,  before  concentration of dissolved  salts  be-
               comes sufficient for  CaSO  4  to be  precipitated.  Interbedded,  unfossiliferous,  fine
               grained, homogeneous carbonates, with anhydrite or gypsum in basinal evaporite
               deposits, attest to this process.
                  The above factors,  which cause formation  of marine CaC0 3  may  be viewed
               collectively as a system of combined special natural processes. All  other sedimen-
               tologic processes operate to modify in one way  or another  the  products  of this
               system. Thus the type of available organisms, sea level fluctuation, rate of subsid-
               ence, hydrographic factors,  and climate,  operate on this  "carbonate factory"  to
               produce the kinds  of limestone and dolomite recognized  in the geologic  record.
               See Fig. XII-1 in the Summary Chapter.



               Carbonate Production Is Basically Organic

               Organisms contribute to detrital deposits of widely varying grain size and, as well,
               form huge masses of precipitated limestone.


               Most Lime Mud Is Organically Derived
               Sedimentologists have  extensively  discussed  its  origin and modes  of accumula-
               tion. It is a common product of shallow, tropical water or the upper layers of the
               open ocean. Cool, marine waters of shallow temperate zones produce only shelly
               and silty carbonate biogenic debris, and planktonic accumulations in ocean basins
               are  composed  mostly  of silt-size  material  formed  in  the  photic  zone  in  lower
               latitudes.
                  Fine lime sediment settles to the bottom without appreciable compaction. A
               few centimeters below the surface the soft sediment consists of about equal por-
               tions of CaC0 3  and water. The carbonate in modern shallow water lime muds is
               generally aragonite, but may contain substantial proportions (up to 50%) of high
               Mg calcite (generally with greater than 10 mol percent Mg in the crystal lattice)
               and as much as  10-15% low magnesium calcite (generally with  less  than  5 mol
               percent Mg).
                  Lime  mud  has  been demonstrated to derive  in  several  different ways:  from
               death  and  decay  of  benthonic  organisms  (mainly  calcareous  algae),  detritus
               abraded from larger carbonate particles, accumulation  of planktonic  biota and
               possibly from direct precipitation from sea water (perhaps biochemically induced
               by phytoplankton blooms). Both low and high Mg calcite deposited in  sea water
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