Extrapolation of laboratory measurements of the viscosity (eta) of sil
icate melts is frequently needed in order to analyze petrological and
volcanological processes. Therefore a general understanding of silicat
e melt viscosities is required. In this paper we survey the present st
ate of our knowledge and distinguish three flow regimes for homogeneou
s silicate liquids: (1) a low-viscosity regime (eta < 1 Pa . s), where
the viscosity obeys a temperature-dependence power law in accordance
with mode coupling theory (these low viscosities are typical for depol
ymerized melts); (2) an intermediate regime (1 < eta < 10(12) Pa . s),
where silicate melt viscosity is determined by the availability of co
nfigurational states (the dependence of the viscosity on the temperatu
re is described aptly by the configurational entropy theory of Adam-Gi
bbs); and (3) a high-viscosity regime, where the liquid has been trans
formed into a glass (eta > 10(12) Pa . s) (this regime is not well kno
wn, but available measurements indicate an Adam-Gibbs or an Arrhenian
temperature dependence of the glass viscosity). Examples are given of
igneous rocks whose geneses were affected by these flow regimes.