The degassing of Cl- and H2O-bearing magmas has been investigated expe
rimentally at similar to 1 bar and 2000 bars and 800-1075 degrees C by
determining the solubility of H2O and Cl- in felsic to intermediate l
iquids variably enriched in F, P, B, C, and excess alkalis or aluminum
. Chloride solubility in H2O-undersaturated silicate liquids is low an
d increases with increasing values of the molar [(Al + Na + Ca + Mg)/S
i] of silicate liquids, F content, and abundance of network-modifying
Al, and pressure. The presence of B or P in peraluminous felsic liquid
s has no discernible influence on Cl- solubility. The experimental sol
ubility data are compared with H2O and Cl- in silicate melt inclusions
from seven high-silica rhyolites and tin and topaz rhyolites of weste
rn North America. Small ranges in Cl- concentration, minimum Cl- conte
nts of 600-800 ppm, large ranges in H2O content, and steeply negative
to near-infinite slopes in plots of H2O vs Cl- for many of the melt in
clusions are similar to abundances and trends of H2O vs Cl- for volati
le phase-saturated felsic liquids, suggesting that some portions of ea
ch of these magmas might have been saturated in volatile phases before
melt inclusion entrapment and eruption.