MEASURING INTERLAYER POTASSIUM RELEASE RATES FROM SOIL MATERIALS - II- A PERCOLATION PROCEDURE TO STUDY THE INFLUENCE OF THE VARIABLE SOLUTE K IN THE LESS-THAN-1 - 10 MU-M RANGE
G. Springob et J. Richter, MEASURING INTERLAYER POTASSIUM RELEASE RATES FROM SOIL MATERIALS - II- A PERCOLATION PROCEDURE TO STUDY THE INFLUENCE OF THE VARIABLE SOLUTE K IN THE LESS-THAN-1 - 10 MU-M RANGE, Zeitschrift fur Pflanzenernahrung und Bodenkunde, 161(3), 1998, pp. 323-329
Release rates of nonexchangeable K from Ap material of a Luvisol ('Eck
erde' loess, 15% clay) are determined using a percolation procedure wh
ich avoids the common artifacts due to shaking or stirring soil;suspen
sions and thus provides less biased kinetic data. CaCl2 solution (10 m
M(c), 20 degrees C, pH 5.8) is percolated through packages of soil agg
regates (0.5-1 mm grain size, 0.5 g samples) with 0.02 to 25 ml h(-1)
Solute K (C-K) was varied between <1 and > 10 mu M and is shown to hav
e a dominant influence on the rates of interlayer K release. These inc
rease exponentially below 3.5 CIM (no steady state but steady decrease
of release rates in each sample). The difference between the related
C-K between moderate and high release rates is as small as 1 mu M K. T
he average rates of a 10-day-interval, starting after 1.3 times the ex
changeable K had been removed, are 40 mu mol K kg(-1) soil d(-1) at 4
mu M C-K and 240 mu mol kg(-1) d(-1) at 3 mu M C-K,C- respectively It
is concluded that larger quantities of interlayer K become plant avail
able in the studied soil if the C-K Of soil solutions gets below 3.5 m
u M (for 10 mM, Ca, 20 degrees C, pH 5.8), probably because the domina
nt dioctahedral illites start to join the release process below this c
ritical limit. The higher K concentration range was accounted for by K
-Ca exchange isotherms which, by alteration of shape, indicate that K-
nex release becomes measurable below 10 to 20 mu M K.It is further arg
ued that existing diffusion or reaction kinetics approaches towards K
release are incomplete because the influence of solute K is not consid
ered.