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￿ acid pH, below 5.0, except in thick E horizons of tropical soils
in which quartz is left and where the pH rises to 6.2 (Schwartz
1986, 1988b);
￿ apparently very low base saturation; this is linked to the overes-
timation of the cation exchange capacity (CEC), at least when it
is determined by the standard method at pH 7; we have already
mentioned this (Chap. 10, § 10.4.2);
￿ free iron content (Fe o , Table 11.4) with maximum in the Bs and
a free aluminium content with maximum in the same horizon
or just below it, in the upper part of the C horizon. The iron
colours the profile yellow or brown, while aluminium oxides are
colourless and so cannot be detected morphologically.
Metal-organic complexes are associations binding the metals (iron and
aluminium) to organic acids. The acids liable to capture these metals
are called complexing agents .
Some authors distinguish metal-organic complexes (binding of the
metal ion to just one acid functional group) and metal-organic chelates ,
in which several reactive sites are involved. But in current usage, the
term complex includes both. Figure 11.3 presents examples.
Concepts of chelates and complexes
O
O
Chelate of
aluminium
C
O -
C
O
+ A1 3+
+ 2 H +
+ H 2 O
Al
OH
OH
O
O
O
Complex of iron
+ H +
O -
+ Fe 2+ + H 2 O
R
C
R
C
O
Fe
OH
Fig. 11.3 Examples of chelate of aluminium and complex of iron (Schnitzer 1984).
The groups having complexing action are, in order of decreasing
affinity for the metal ions:
-O-, -NH 2 , -N=N-, =N (aromatic), COO-, -O-, C=O
In some cases, complexation involves a hydrogen bond.
Apart from aluminium and iron, many other metals are liable to be
complexed (Pb, Cr, etc.). But the special attention given to Al and Fe is
 
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