Page 173 - Petrology of Sedimentary Rocks
P. 173

to  bits  by  wave   action   to  form   rounded,   polished   coquinas.   Such  supermature   pelecypod
       biosparites   formed   a  semicircular   beach   coquina   around   the  north   flank   of  Pilot   Knob,   a
       Cretaceous   submarine   volcano   near   Austin   (R.  White).   Often,   the  well-sorted   (mature)
       ones   are  made   up  of   one   fossil   type,   e.g.,   pelecypod   fragments,   crinoid   columnals,
       forams,   or   fusulinids;   the   poorly   sorted   (submature)   ones   are   made   up  of   diverse
       mixtures   of  fossils   of  inherently   different   size,  e.g.  forams   plus  crinoids,   or  brachiopods
       plus   bryozoans   plus  fusulinids.   Thus  sorting   is  believed,   as  in  terrigenous   rocks,   to  be
       largely   a  function   of   source   (i.e.   available   types   of  fossils),   with   environment   (i.e.
      strength   of   waves   and   currents,   or   water   depths)   playing   a  modifying,   but   not
       controlling   role.   Sorting   is  best   in  shallower   waters   or  on  the  beach   itself,   and  gets
       worse   offshore.   Thus   in  moving   from   a  beach   surf   zone  into   deeper   waters   one  might
       theoretically   expect   the  sequence   to  go  from   supermature   biosparite   (well   rounded   and
      sorted)   to  mature   (sorted   but  only   slightly   rounded)   to  submature   (unsorted,   fragments
       not   rounded   but   possibly   broken)   to  biomicrite   (immature,   with   unsorted,   broken   or
      whole   fossils)   and   finally   micrite.   This   sequence   would   undoubtedly   be  modified   by
       types   of  fossils   available   and  wave   energy   of  the  coast.   See  I962   AAPG   Mem   I’/ I  and
       1964  JG  (Folk   &  Robles)   for  details.

             In  some   areas,   shoal   regions   and  littoral   zones   are  characterized   by  algal,   coral,
      or  other   types   of  reefs.   Most   reef-forming   organisms   live   in  the  shallow   waters   where
      there   is  still   sunlight   available   for   photosynthesis   of  the  algae,   which   make   up  the  bulk
      of  living   tissue   on  most   reefs   (Odum).   Reef   rocks   (biolithites)   are  exceedingly   complex,
      because   of   (I)   abundant   life   and   many   different   types   of   fossils,   making   rock
      petrographically   varied,   especially   the  algae   (there   is  probably   as  much   complexity   and
      variety   of  external   form   and  internal   structure   in  algae   as  there   is  in  all  other   fossils
      put  together),   (2)  the  fantastic   growth   forms   assumed   by  many   of  the   reef   organisms,
      with   weird   branching,   bushy   or  encrusting   habits,   (3)  the   reef   rock   is  riddled   with
      cavities   which   may  be  empty   (and  later   filled   with   spar  in  fibrous   or  mosaic   forms),   or
      cavities   may   be  partly   filled   with   terrigenous   sand,   intraclasts,   lime   mud,   pellets,
      organisms   that   lived   in  the   cavity,   and  inswept   broken   fossil   debris.   Add   to  this   the
      fact   that   reefs   are   prone   to  patchy   recrystallization   (because   of  the   high   aragonite
      content)   and  one  can  see  that   a  thin   section   will   be  of  the  utmost   complexity.   Reefs,
      although   they   usually   thrive   in  high-energy   zones,   act  as  baffles   to  the  current,   and  the
      water   movement   down   in  the  crevices   and  pockets   between   branching   organisms   may  be
      relatively   calm   even   in  a  surf   zone,   just  as  the  interior   of  a  forest   may  be  calm   in  a
      windy   day.   Hence   reefs   are  associated   with   much   micrite   and  fine   debris   which   filters
      down   between   the   branching   growths   and  cannot   be  dislodged.   In  fact,   stromatolitic
      reefs,   probably   formed   by  blue-green   algae,   are  largely   micrite,   presumably   trapped   by
      the  slimy   algal   mats  and  then  firmly   bound   together   by  the  filaments.

            Rocks   of  type   II  and  type   III  (either   pure   micrite   or  rocks   with   a  micrite   matrix)
      indicate   formation   in  areas   of  ineffective   winnowing   and  calm   currents.   These   can
      form   in  four   important   ways:   (I)   in  protected   lagoons,   in  which   the   water   is  very
      shallow,   perhaps   not  more   than   a  few   feet   deep;   (2)  in  broad,   shallow   platforms   on  the
      lee  side  of  barriers   (e.g.  west   side  of  Andros   Island,   Bahamas),   where   the  great   width   of
      the   platform   prevents   any  permanent   removal   of  lime   mud   and   it  is  merely   shifted
      around;   (3)  in  moderately   deep  waters   in  geosynclines   (probably   down   to  a  few  hundreds
      of  feet);   (4)  as  open-ocean   Chalks;   (5)  as  Ginsberg   has  shown,   lime   mud  may  accumulate
      locally   around   organic   baffles   (marine   grasses,   coral   or  algal   growths)   even   in  fairly
      high-energy   environments.    To  tell   these   micrite-rich   environments   apart   is  often   a
      difficult   problem   as  they  may  represent   very   shallow   or  moderately   deep  areas.   Several
      criteria   are  useful.   Among   the  best  criteria   is  the  fossil   content.   For  example,   clams
      or  oysters   in  micrite   would   indicate   a  shallow,   perhaps   lagoonal   area,   whereas   an
      exclusively   pelagic   fauna   of  small   forams   would   probably   be  indicative   of  deeper   water





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