The viscosities of a series of water-bearing peralkaline rhyolitic mel
ts have been experimentally determined. The dry melt compositions are
composed of a series of additions of Na2O to a metaluminous base compo
sition. The melts, initially hydrated at high pressures and quenched i
sobarically, have been prepared by cutting and polishing, then reheati
ng across the glass transition at 1 arm where they an annealed to a re
laxed metastable state and then investigated dilatometrically using mi
cropenetration methods. The measurements have been performed in the vi
scosity range of 10(8.5)-10(11.5) Pa s which corresponds to temperatur
es in the range of 675-220 degrees C for these compositions. Despite t
he relatively low viscosities of dry peralkaline melts in comparison w
ith metaluminous melts of similar SiO2 content, the viscosities of per
alkaline rhyolitic melts also decrease strongly and non-linearly with
the addition of water. The resulting viscosity-temperature relationshi
ps for water-bearing peralkaline rhyolitic melts are shifted to much l
ower temperatures such that glass transition temperatures for moderate
cooling rates correspond to extraordinarily low temperatures. A model
is presented for the calculation of melt viscosities in the range of
10(8.5)-10(11.5) Pa s for peralkaline rhyolites with up to 7 wt% H2O.
The very fluid nature of these peralkaline rhyolites over a wide range
of water contents may facilitate a very efficient degassing history o
f glassy peralkaline rhyolites in nature. Efficient degassing might ex
plain the apparent contradiction of the presence of common water-rich
melt inclusions in phenocryst phases hosted in water-foe glassy rhyoli
tes, versus the absence of vesicular layers or textural evidence for a
vesicular past for the glassy rocks. (C) 1998 Elsevier Science B.V. A
ll rights reserved.