Partitioning of 41 elements between solids and water was studied by filtrat
ion and dialysis in situ in Czech freshwaters. Field-based distribution (pa
rtition) coefficients, K-D, between suspended particulate matter (SPM) and
filtrate ('dissolved' fraction) differed by 4 orders of magnitude. The high
est K-D values (log K-D > 2.0 l/g) were exhibited by Zr, Al, Ce, Pb, La, Ti
, Fe, Sm, Th and Cr which are extremely insoluble in near-neutral water or
generally poorly soluble (Zr,Ti). The K(D)s decrease with element and DOC l
oading due to the relative increase of the element in the low molecular fra
ction. Log K-D mostly increased linearly with pH within a range from 3.5 to
9. K-D(U) decreased at pH >6 due to carbonate complexation. The colloidal
fraction (> 1 kDa < 0.4 <mu>m) in a reservoir with a pH of 6.8 was mainly p
referred by Fe, Pb, Be, Nb, Y, Al, Ni, U and Zr. When the colloidal fractio
n is not differentiated from true solution, then incorrect information abou
t partitioning may be obtained and the highest K-D may decrease. (C) 2001 E
lsevier Science Ltd. All rights reserved.