Rc. Pearce et Me. Sumner, APPARENT SALT SORPTION REACTIONS IN AN UNFERTILIZED ACID SUBSOIL, Soil Science Society of America journal, 61(3), 1997, pp. 765-772
The equivalent retention of Ca2+ and SO42- from gypsum solutions in ac
id subsoils has recently been reported. The term salt sorption has bee
n coined to describe this process, yet little is known about the natur
e of the reactions involved. This study was conducted to determine if
other cation-anion combinations would exhibit similar behavior and to
examine the extractability of the sorbed ions. An unfertilized acid Ce
cil (clayey, kaolinitic, thermic Typic Kanhapludult) subsoil was equil
ibrated using a saturated paste technique, with solutions of six diffe
rent salts at a loading rate of approximate to 14.0 mmol(c) kg(-1). Th
e salt solutions used were CsSO4, MgSO4, Na2SO4, CaCl2, MgCl2, and a d
eionized water control. This soil exhibited salt sorption with all six
electrolyte solutions. The SO4 salts were almost;completely sorbed wi
th both cation and anion uptake on the order 13.8 mmol(c) kg(-1). Calc
ium and magnesium chloride were sorbed at approximate to 11.7 mmol(c)
kg(-1) and NaCl was sorbed at 8.2 mmol(c) kg(-1). The treated soils we
re air dried and extracted with successive portions of deionized water
or 0.5 M NH4NO3. A relatively large proportion of both cations and an
ions were removed by repeated extraction with water, suggesting that i
onic strength played an important role in the salt sorption process. N
early all of the sorbed cations and Cl- were recovered by neutral salt
extraction, but <100% of he SO42- could be accounted for by neutral s
alt extraction. Neutral salt extractable Al was significantly reduced
by salt treatment It appeared that salt sorption in this soil may have
resulted from several mechanisms including precipitation, specific ad
sorption, ionic strength induced charging, and ion pair adsorption ope
rating concurrently.