L. Hopkinson et al., The nature of crystalline silica from the TAG submarine hydrothermal mound, 26 degrees N Mid Atlantic Ridge, CONTR MIN P, 137(4), 1999, pp. 342-350
Silica occurs in abundance in a variety of hydrothermal samples from the Tr
ans-Atlantic Geotraverse (TAG) hydrothermal mound, 26 degrees N Mid-Atlanti
c Ridge. The water content, trace element chemistry, and mineralogy of crys
talline silica from 15 different samples have been examined by vibrational
spectroscopy and probe microanalysis. The samples are from: shallow subsurf
ace ferric iron oxyhydroxide silica deposits (n = 4), a fragment of an acti
ve white smoker chimney (n = 1), anhydrite bearing hydrothermal breccias (n
= 2), pyrite silica breccias (n = 3), and silicified wall rock breccias (n
= 5). Length-fast chalcedony occurs in association with variable quantitie
s of ferric iron oxyhydroxides in hydrothermal breccias from the mound flan
ks, within shallower subsurface chert samples, and within white smoker chim
ney walls. Samples from the anhydrite zone contain textures which are sugge
stive of an origin involving replacement of anhydrite, Samples taken from T
AG I and 5 from below the anhydrite zone contain no chalcedony. Instead the
y contain subhedral quartz crystals which show oscillatory zoning in alumin
ium. Two types of crystalline silica namely, type A and type B quartz, are
defined on the basis of the infrared spectra in the OH region from 3200 cm(
-1) to 3600 cm(-1). The type A quartz occurs beneath the anhydrite zone at
TAG 1 and 5. We propose a model that relates specific varieties of crystall
ine silica to different thermal and chemical environments within the mound
interior, Length-fast chalcedony occurs in an outer low temperature envelop
e across the top and sides of the mound. The common association between len
gth-fast chalcedony and ferric iron oxyhydroxides suggests that chalcedony
crystallization is favoured where catalysis by ferric iron can occur, The a
pparent suppression of fibrous silica at the expense of single quartz cryst
als with increasing depth is attributed to differing growth rates and degre
es of supersaturation of silica-bearing solutions with increasing temperatu
re within the mound. The transition from type A to type B single crystal gr
owth is interpreted to occur at temperatures approaching similar to 360 deg
rees C due to decreasing solubility of aluminium in quartz, so that alumini
um is rendered unavailable for type A valence compensation.