Curves for P adsorption by ferric hydroxide in the presence of citrate
and tartrate were prepared. From the curves, it appeared as though ta
rtrate at 10(-4) M has no effect on P adsorption up to 750 mu mol P g(
-1) ferric hydroxide adsorbed. However, observation of flocculation pa
tterns show that even when the curves are identical, there is a differ
ence in the way P is adsorbed in the presence of tartrate and citrate
in terms of the type of site that is attacked. Assessment of phosphate
- citrate competition using P-32 and C-14 showed that citrate is less
readily adsorbed by ferric hydroxide than tartrate and that citrate d
issolves adsorption sites more readily than tartrate. The implications
of this study are that root exudates containing a greater amount of t
artrate would cause more efficient use of added P by plants since tart
rate occupies the high affinity sites and therefore reduces phosphate
fixation. Plants which produce root exudates high in citrate content w
ould be able to utilize more fixed P than plants which produce exudate
s lower in citrate content because citrate dissolves sites at which P
is held.