The structural and chemical evolution of palagonite was studied as a functi
on of glass composition, alteration environment, and time by applying a ran
ge of analytical methods (electron microprobe, infrared photometry, atomic
force microscopy, X-ray fluorescence, and X-ray diffraction). Palagonitizat
ion of volcanic glass is a continuous process of glass dissolution palagoni
te formation, and palagonite evolution, which can be subdivided into two di
fferent reaction stages with changing element mobilities. The first stage i
s characterized by congruent dissolution of glass and contemporaneous preci
pitation of "fresh," gel-like, amorphous, optically isotropic, mainly yello
wish palagonite. This stage is accompanied by loss of Si, Al, Mg, Ca, Na, a
nd K, active enrichment of H2O and the passive enrichment of Ti and Fe. The
second stage is an aging process during which the thermodynamically unstab
le palagonite reacts with the surrounding fluid and crystallizes to smectit
e. This stage is accompanied by uptake of Si, Al, Mg, and K from solution a
nd the loss of Ti and H2O. Ca and Na are still showing losses, whereas Fe r
eacts less consistently, remaining either unchanged or showing losses. The
degree and direction of element mobility during palagonitization was found
to vary mainly with palagonite aging, as soon as the first precipitation of
palagonite occurs. This is indicated by the contrasting major element sign
atures of palagonites of different aging steps, by the changes in the direc
tion of element mobility with palagonite aging, and by the general decrease
of element loss with increasing formation of crystalline substances in the
palagonite. Considering the overall element budget of a water-rock system,
the conversion of glass to palagonite is accompanied by much larger elemen
t losses than the overall alteration process, which includes the formation
of secondary phases and palagonite aging. The least evolved palagonitized m
afic glass studied has undergone as much as 65 wt% loss of elements during
palagonite formation compared to similar to 28 wt% element loss during bulk
alteration. About 33 wt% element loss was calculated for one of the more e
volved, in terms of the aging degree, rocks studied, compared to almost no
loss for bulk alteration.