Role of saline fluids in deep-crustal and upper-mantle metasomatism: insights from experimental studies

• Published in: Geofluids Vol. 10; no. 1-2; pp. 58 - 72
• Main Authors: NEWTON, R. C., MANNING, C. E.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.05.2010
• Subjects: experimental petrology; metamorphic fluids; mineral solubility; salt effects
• ISSN: 1468-8115; 1468-8123
• DOI: 10.1111/j.1468-8123.2009.00275.x

Geofluids (2010) 10, 58–72 Chloride‐rich brines are increasingly recognized as playing an important role in high pressure and temperature metamorphic and magmatic systems. The origins of these saline multicomponent fluids are debated, but experimental evidence suggests that regardless of their origin they must be important agents of rock alteration and mass transfer wherever they occur. Studies of the solubility of quartz in H2O, CO2–H2O and salt–H2O solutions provide a framework for understanding the role of brines in the deep crust and upper mantle. While quartz solubility in the system SiO2–H2O–NaCl–CO2 is maximal at a given high pressure and temperature if the solvent is pure H2O, the decline in quartz solubility with NaCl content (salting‐out) is less severe than in CO2–H2O fluids at comparable H2O activities. Moreover, at lower pressures, quartz solubility initially salts in at low salt contents, before reaching a maximum and then declining. The behavior of quartz solubility in salt–H2O solutions has not yet been fully explained and is the subject of active debate. Experimental investigations of the solubility of some other rock‐forming oxides and silicates show enhancements due to NaCl addition. As illustrated by the well‐studied CaO–Al2O3–SiO2–NaCl–H2O system, enhancements initially increase to maxima, and then decline. This behavior can be explained by formation of a range of hydrated aqueous complexes and clusters with specific NaCl:H2O stoichiometries. In contrast, solubilities of calcium salts, including calcite, fluorite, fluorapatite and anhydrite, rise monotonically with increasing NaCl, implying complexing to form anhydrous ionic solutes and/or ion pairs. The experimental studies offer new insights into fluid‐rock interaction in a range of settings, including carbonatite–fenite complexes, granulite‐facies metamorphism, porphyry ore deposits and aluminum‐silicate vein complexes in high‐grade metamorphic terranes.