Page 41 - Geochemical Remote Sensing of The Sub-Surface
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18                                                    O.F. Putikov and B.  Wen
           occur  as  ions,  complex  ions  and  compounds.  Their  absolute  concentrations  are  of the
           order  of  1-20  •  10 .2  ~tg/l and  their  relative  concentrations  as  compared  with  their  total
           contents  in  the  rocks  usually  ranges  from  0  to  0.2%,  and  is  rarely  greater  than  2%
           (Antropova,  1975).  In  capillary  moisture  the  absolute  concentrations  of Pb  and  Cu  are
           about  10-2-102 ~tg/1 and  the  relative  concentrations  of  these  metals  are  about  0.1-1%
           (Antropova,  1975).  Absolute  concentrations  of  sorbed  metals  are  10-1-102 ~tg/l for  Pb
           and 6 •  10 .3 to 4.7  •  102 ~tg/1 for Mo, and their relative  concentrations  are  about  1% and
           for Pb  and  0.01-0.1%  for Mo.  Antropova  (1975)  showed that after extraction  of heavy
           metals  soluble  in  groundwater,  capillary  moisture  and  sorbed  forms,  a  significant
           fraction  of metals  is  still  held  by  chemical  bonds  of  different  strengths  in  oxides  and
           hydroxides  of Fe  and  Mn.  The  relative  content  of this  form of metals  is usually  1-10%
           for Cu and Ni, up to 90% (frequently  16.5-86%)  for Pb and up to 93%  for Mo.  A  metal
           may  also  form  compounds  with  natural  organic  acid,  making   metallo-organic
           compounds  (MOC).  Antropova  (1975)  found  that  fulvic  and  humic  acids  are  special
           concentrators  of heavy metals and the metals they concentrate  exist not as cations but as
           constituents  of humate  and fulvate  complexes.  In these  complexes  the  concentrations  of
           metals  are  usually  higher  than  the  a~erage  metal  concentrations  in  the  total  organic
           fraction.  Several  researchers  (Krat,  1983;  Malmqvist  and  Kristiansson,  1984;
           Kristiansson  and  Malmqvist,  1986;  Krchmar,  1988;  Dukhanin,  1990;  Putikov  and
           Dukhanin;  1994)  have  pointed  out  that,  in  the  upper  crust  and  in  the  near-surface
           atmosphere,  heavy  metals  exist  in  the  gas  phase.  But  the  concentration  of elements  in
           this  phase  is  very  low,  of  the  order  of  10 .4  pg/1 (Dukhanin,  1990;  Ozerova  and
           Mashianov,  1989).
              In  physico-chemical  terms,  metals  in  these  different  forms  are  held  by  chemical
           bonds  of different  strengths.  According  to the  strength of the  chemical  bonds,  the  forms
           of metals  may be divided into four groups:

            9  strongly confined (strong chemical bonds within minerals);
            9  moderately confined (MOCs and Fe-Mn hydroxides);
            9  weakly confined (metals in capillary moisture, sorbed on surfaces);
            9  mobile (soluble  in groundwater, quasi-gaseous and gaseous).

              The  capacity  of metals  to  disperse  in  space  is  clearly  related  to  this  classification:
           weakly-confined metals  are  able  to disperse  for greater distances  than  strongly-confined
           metals,  and  so  on.  In  particular,  mobile  forms  are  able  to  migrate  far  from  their
           sourcesprovided  that  some  natural  or  artificial  physical  field  is  exerted  to  effect
           migration.  However,  all  forms  are  in a  state  of dynamic  equilibrium  and  can  transform
           into other forms.  One consequence  is that, with increasing concentration of metals  in the
           more  mobile  forms,  there  is  a  simultaneous  increase  in  concentration  of metals  in  the
           forms with stronger chemical bonds. For example,  dissolved Pb, Mo and Cu will interact
           with oxides  and hydroxides of Fe  and Mn under certain physico-chemical  conditions  of
           pH  and  Eh.  First,  due  to  adsorption  of  these  metals  from  solution,  the  metals  are
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