“…Remnants of hornblende grains typically show highly etched but clean surfaces, essentially free of smectite (Figure 7). Similar observations of amphibole dissolution have been reported by Berner and Schott (1982), Anand and Gilkes (1984), and Velbel (1989) and were interpreted as reflecting a relatively open hydrologic regime, A more closed system might produce smectite replacement of amphibole or pyroxene (e.g., Eggleton, 1975;Banfield and Barker, 1993). At Uley, the pattern of NAu-2 distribution is consistent with brittle fracturing of the amphibolite and infiltration of fluid that preferentially dissolved hornblende (and pyroxene?)…”
Section: Clay Distribution and Nontronite Formationsupporting
confidence: 79%
“…Ca-rich amphibole, of composition approximating alumino-ferro-hornblende (EDX analyses), was usually restricted to the central portion of rock fragments, away from areas of high nontronite concentration. Most grains examined showed extensive dissolution via crystallographically controlled etch pits (Figure 7) resulting in cavernous voids lined with sharp dentate projections, a common characteristic of advanced amphibole weathering (e.g., Berner and Schott, 1982; A n a n d and Gilkes, 1984;Velbel, 1989). Although clay products were observed as thin coatings on the surface of some amphibole grains, voids formed by dissolution were typically clean and free of any obvious secondary crystallization products (Figure 7).…”
Abstrac~Mining operations during the early 1990s at Uley Graphite Mine near Port Lincoln on southern Eyre Peninsula, South Australia, uncovered abundant nontronite veins in deeply weathered granulite facies schist, gneiss, and amphibolite of Palaeoproterozoic age. Two types of nontronite are present: a bright yellowish-green clay (NAu-1) distributed as veinlets and diffuse alteration zones within kaolinized schist and gneiss, and a massive to earthy, dark-brown clay (NAu-2) infilling fracture networks mainly in amphibolite or basic granulite. The nontronites are the product of low-temperature hydrothermal alteration of primary minerals, biotite, and amphibole. The principal chemical difference between NAu-1 and NAu-2 is a higher alumina content in NAu-1, which was either inherited during hydrothermal alteration of biotite in the host rock or acquired through recrystallization of nontronite during subsequent weathering and associated kaolinization. Sufficient bulk samples of both NAu-1 and NAu-2 were collected to supplement reference nontronite of the Source Clay Repository of The Clay Minerals Society. The clay fraction of the bulk samples is typically >85%. NAu-1 contains minor kaolin and quartz which are easily removed to give a high purity nontronite of composition M+105[Si6.98Al102]
“…Remnants of hornblende grains typically show highly etched but clean surfaces, essentially free of smectite (Figure 7). Similar observations of amphibole dissolution have been reported by Berner and Schott (1982), Anand and Gilkes (1984), and Velbel (1989) and were interpreted as reflecting a relatively open hydrologic regime, A more closed system might produce smectite replacement of amphibole or pyroxene (e.g., Eggleton, 1975;Banfield and Barker, 1993). At Uley, the pattern of NAu-2 distribution is consistent with brittle fracturing of the amphibolite and infiltration of fluid that preferentially dissolved hornblende (and pyroxene?)…”
Section: Clay Distribution and Nontronite Formationsupporting
confidence: 79%
“…Ca-rich amphibole, of composition approximating alumino-ferro-hornblende (EDX analyses), was usually restricted to the central portion of rock fragments, away from areas of high nontronite concentration. Most grains examined showed extensive dissolution via crystallographically controlled etch pits (Figure 7) resulting in cavernous voids lined with sharp dentate projections, a common characteristic of advanced amphibole weathering (e.g., Berner and Schott, 1982; A n a n d and Gilkes, 1984;Velbel, 1989). Although clay products were observed as thin coatings on the surface of some amphibole grains, voids formed by dissolution were typically clean and free of any obvious secondary crystallization products (Figure 7).…”
Abstrac~Mining operations during the early 1990s at Uley Graphite Mine near Port Lincoln on southern Eyre Peninsula, South Australia, uncovered abundant nontronite veins in deeply weathered granulite facies schist, gneiss, and amphibolite of Palaeoproterozoic age. Two types of nontronite are present: a bright yellowish-green clay (NAu-1) distributed as veinlets and diffuse alteration zones within kaolinized schist and gneiss, and a massive to earthy, dark-brown clay (NAu-2) infilling fracture networks mainly in amphibolite or basic granulite. The nontronites are the product of low-temperature hydrothermal alteration of primary minerals, biotite, and amphibole. The principal chemical difference between NAu-1 and NAu-2 is a higher alumina content in NAu-1, which was either inherited during hydrothermal alteration of biotite in the host rock or acquired through recrystallization of nontronite during subsequent weathering and associated kaolinization. Sufficient bulk samples of both NAu-1 and NAu-2 were collected to supplement reference nontronite of the Source Clay Repository of The Clay Minerals Society. The clay fraction of the bulk samples is typically >85%. NAu-1 contains minor kaolin and quartz which are easily removed to give a high purity nontronite of composition M+105[Si6.98Al102]
“…In contrast to the hornblende crystals in the corestone and in the rindlet zone, hornblende crystals in the protosaprolite zone are significantly smaller and dramatically etched ( Figure 6). Similar sawtoothed etching along weathered hornblende cleavage planes has been reported by others (e.g., Berner and Schott, 1982;Anand and Gilkes, 1984;Velbel, 1989). Hornblende grains are extremely difficult to find under SEM above the rindlet-saprolite interface, although XRD patterns indicate that hornblende persists in the first 2 cm of the saprolite, but not beyond.…”
Section: Chemical Mobilitysupporting
confidence: 78%
“…Hornblende is the most abundant Fe-silicate in the bedrock, but the mechanism and location of hornblende weathering has not been previously identified. Pseudomorphic replacement of hornblende by clay minerals such as chlorite, chlorite-saponite, or saponite has been documented in soil and saprolite (Wilson and Farmer, 1970;Anand and Gilkes, 1984), but no widespread evidence for such phase changes was observed in the present samples. Similarly, dissolution of hornblende and re-precipitation of iron (oxy)hydroxides, gibbsite, or kaolinite can occur in soil, saprolite, and weathering rinds ( e.g., Velbel, 1989), but was not observed in the rindlet samples: i.e., we observed no etching of the hornblende grains, no boxwork texture or precipitates associated with (Figure 4d).…”
“…Dissolution-reprecipitation mechanisms have been invoked on petrographic grounds to explain several occurrences of pyribole weathering (e.g., Berner and Schott, 1982;Glasmann, 1982), serpentinization (e.g., Cressey, 1979), feldspar weathering (e.g., Grant, 1963Grant, , 1964Koppi and Williams, 1980;Anand and Gilkes, 1984;Anand et aL, 1985), and pseudomorphous clay replacements after plagioclase feldspar, which appear to preserve twinning in clay pseudomorphs (Velbel, 1983). Transport of ostensibly "immobile" elements in dissolved form is also required to account for the composition of pseudomorphous weathering products of ferromagnesian silicates.…”
Section: Dissolution-reprecipitation Mechanism and The Stoichiometry mentioning
Abstract--Hornblende of the Carrol Knob mafic complex (southern Blue Ridge Mountains, North Carolina) has weathered under humid, temperate conditions. Hornblende weathering appears to have been a dissolution-reprecipitation reaction, in which hornblende dissolved stoichiometrically, and the ferruginous and aluminous weathering products (goethite, gibbsite, and kaolinite) precipitated from solution (neoformation). During the earliest stage of alteration, ferruginous weathering products formed as linings of fractures within and around crystals and cleavage fragments of hornblende. Side-by-side coalescence of lenticular etch pits during more advanced weathering produced characteristic "denticulated" terminations on hornblende remnants in dissolution cavities bounded by ferruginous boxworks. Dissolution cavities are devoid of weathering products. Small "pendants" of ferruginous material project from the boxwork into void spaces. Because these products are separated from the hornblende remnants by void space, they must have been produced by dissolution-reprecipitation reactions. Complete removal of the parent hornblende left a ferruginous microboxwork or "negative pseudomorph." Only A1 and Fe were conserved over microscopic distances; alkali and alkaline-earth elements were stoichiometrically removed from the weathering microenvironment during the weathering process.
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