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                                                                            THE ROLE OF VOLATILES  67


                                                                    Dissolved gas (wt%)
                                                   0              0.5             1              1.5
                                                  0                                                0
                                                                                      H 2 O in rhyolite
                                                                         H 2 O in basalt
                                                 50
                                                                                                   2



                                               Pressure (MPa)  100  CO 2                           4  Depth (km)




                                                150
                                                                                                   6
                 Fig. 5.3 A comparison of the solubility
                 of H O in rhyolite and basalt and of
                    2
                 CO in either magma as a function of
                    2                           200
                 pressure and corresponding depth
                 beneath the surface. The lower
                                                                                                   8
                 solubility of CO means that it tends to
                            2
                  exsolve from magmas at much greater
                  depths beneath the surface than H O.  250
                                         2
                  depth of ∼0.35 km. For H O in rhyolite, exsolution  the overlying rocks causing considerable release
                                      2
                  begins at an even shallower depth (Fig. 5.3). The   of CO in the summit caldera. The magma in the
                                                                   2
                  situation is actually more complicated when two  chamber, though, is still likely to be undersaturated
                  volatiles are present because as soon as the less   in H O at all depths within the magma chamber,
                                                                  2
                  soluble volatile starts to exsolve, a very small  and so when the magma is eventually erupted it
                  amount of the more soluble volatile is also released.  tends to have lost most of its CO but none of its
                                                                                         2

                  Fortunately, it is generally accurate enough to treat  H O. As a result, H O will be the most important
                                                                              2
                                                               2
                  the solubilities of the two components as though  volatile in driving the eruption. This kind of beha-
                  they were independent.                      vior has been observed in real volcanic systems such
                                                              as Kilauea volcano in Hawai’I. Other effects of exso-
                   The difference between the depths at which CO
                                                          2   lution of magma in magma chambers have been
                 and H O tend to exsolve can affect the behavior of
                      2                                       discussed in Chapter 4.
                 the magmatic system as a whole. Say, for example,
                 that beneath the summit caldera of a volcano there
                 is a magma chamber with its top at a depth of ∼2km
                                                              5.4 Bubble nucleation
                 and its bottom at ∼6 km, and that basaltic magma
                 is fed to the chamber from below. By the time the
                 magma enters the chamber, the low solubility of  In principle, bubbles should nucleate in magmas as
                 CO (Fig. 5.3) will generally mean that the magma  soon as the least soluble volatile species becomes
                    2
                 has already become supersaturated in this volatile,  saturated in the melt. However, the process of bub-
                 and so the magma will reach the chamber already  ble nucleation is not trivial. By definition it involves
                 containing some CO bubbles.                  the coming together of a sufficiently large number
                                  2
                   Bubbles of CO forming in the stored magma will  of molecules to form a stable bubble: if the bubble
                               2
                 rise through it to the roof of the magma chamber.  that tries to form is too small, the force of surface
                 Often this CO will then seep out through cracks in  tension acts to try to shrink the bubble which, at
                            2
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