Subsolvus

About: Subsolvus is a research topic. Over the lifetime, 81 publications have been published within this topic receiving 9365 citations.

A-type granites: geochemical characteristics, discrimination and petrogenesis

Abstract: New analyses of 131 samples of A-type (alkaline or anorogenic) granites substantiate previously recognized chemical features, namely high SiO2, Na2O+K2O, Fe/Mg, Ga/Al, Zr, Nb, Ga, Y and Ce, and low CaO and Sr. Good discrimination can be obtained between A-type granites and most orogenic granites (M-, I and S-types) on plots employing Ga/Al, various major element ratios and Y, Ce, Nb and Zr. These discrimination diagrams are thought to be relatively insensitive to moderate degrees of alteration. A-type granites generally do not exhibit evidence of being strongly differentiated, and within individual suites can show a transition from strongly alkaline varieties toward subalkaline compositions. Highly fractionated, felsic I- and S-type granites can have Ga/Al ratios and some major and trace element values which overlap those of typical A-type granites. A-type granites probably result mainly from partial melting of F and/or Cl enriched dry, granulitic residue remaining in the lower crust after extraction of an orogenic granite. Such melts are only moderately and locally modified by metasomatism or crystal fractionation. A-type melts occurred world-wide throughout geological time in a variety of tectonic settings and do not necessarily indicate an anorogenic or rifting environment.

Nature and origin of A-type granites with particular reference to southeastern Australia

Abstract: In the Lachlan Fold Belt of southeastern Australia, Upper Devonian A-type granite suites were emplaced after the Lower Devonian I-type granites of the Bega Batholith. Individual plutons of two A-type suites are homogeneous and the granites are characterized by late interstitial annite. Chemically they are distinguished from I-type granites with similar SiO2 contents of the Bega Batholith, by higher abundances of large highly charged cations such as Nb, Ga, Y, and the REE and lower Al, Mg and Ca: high Ga/Al is diagnostic. These A-type suites are metaluminous, but peralkaline and peraluminous A-type granites also occur in Australia and elsewhere. Partial melting of felsic granulite is the preferred genetic model. This source rock is the residue remaining in the lower crust after production of a previous granite. High temperature, vapour-absent melting of the granulitic source generates a low viscosity, relatively anhydrous melt containing F and possibly Cl. The framework structure of this melt is considerably distorted by the presence of these dissolved halides allowing the large highly charged cations to form stable high co-ordination structures. The high concentration of Zr and probably other elements such as the REE in peralkaline or near peralkaline A-type melts is a result of the counter ion effect where excess alkali cations stabilize structures in the melt such as alkali-zircono-silicates. The melt structure determines the trace element composition of the granite. Separation of a fluid phase from an A-type magma results in destabilization of co-ordination complexes and in the formation of rare-metal deposits commonly associated with fluorite. At this stage the role of Cl in metal transport is considered more important than F.

From orogenic to anorogenic settings: Evolution of granitoid suites after a major orogenesis

Abstract: Many orogenic belts display associations of calc-alkaline and alkaline igneous centres which are closely related in space and time. The sequence: calc-alkaline batholithuplift and unroofingalkaline plutonic–volcanic complexes, lasts less than 100 Ma and documents a very fast switch from orogenic to anorogenic geodynamic conditions. The magmatic suites have a mantle origin with decreasing crustal contribution, but the sources and the types of differentiation processes differ. Alkaline granites can be subdivided in two groups: 1 Post-orogenic Ba and Sr-rich red granites having Mg-rich mafic minerals and high content of Mn whether they are peralkaline or peraluminous. Crustal contribution is indicated by Sr isotopic signatures. Water-rich fluids are responsible for the subsolvus crystallization of alkali feldspars and for the high oxygen fugacity. Magmatic centres were emplaced less than 10 Ma after the late-orogenic formations. 2 Early anorogenic Ba and Sr-poor greenish to whitish hypersolvus granites having Fe-rich mafic minerals, low contents of Mn, and virtually no Mg F-rich aqueous fluids are probably less abundant and promote subsolidus hydrothermal alteration with only subordinate late-stage oxidation. Crustal contamination can be ruled out for the non-mineralized complexes, but can be important in the hydrothermal mineralized areas. The magmatic centres are considerably younger than the first group. During the first 100 Ma following the end of a major orogeny, a new mantle source replaces the old complex system of mixed oceanic–continental crust-mantle sources and produces alkaline melts which are subsequently less and less contaminated by crustal host rocks. Relations between hydrothermal events, mineralizations, and crustal isotope signatures suggest that crustal contribution relates to percolating fluids and not to anatexis of lower and/or middle crust.

Status of thermobarometry in granitic batholiths

Abstract: Most granitic batholiths contain plutons which are composed of low-variance mineral assemblages amenable to quantification of the P– conditions that characterise emplacement. Some mineral thermometers, such as those based on two feldspars or two Fe–Ti oxides, commonly undergo subsolidus re-equilibration. Others are more robust, including hornblende–plagioclase, hornblende–clinopyroxene, pyroxene–ilmenite, pyroxene–biotite, garnet–hornblende, muscovite-biotite and garnet–biotite. The quality of their calibration is variable and a major challenge resides in the large range of liquidus to solidus crystallisation temperatures that are incompletely preserved in mineral profiles. Further, the addition of components that affect Kd relations between non-ideal solutions remains inadequately understood. Estimation of solidus and near-solidus conditions derived from exchange thermometry often yield results >700°C and above that expected for crystallisation in the presence of an H2O-rich volatile phase. These results suggest that the assumption of crystallisation on an H2O-saturated solidus may not be an accurate characterisation of some granitic rocks.Vapour undersaturation and volatile phase composition dramatically affect solidus temperatures. Equilibria including hypersthene–biotite–sanidine–quartz, fayalite–sanidine–biotite, and annite–sanidine–magnetite (ASM) allow estimation of Estimates by the latter assemblage, however, are highly dependent on . Oxygen fugacity varies widely (from two or more log units below the QFM buffer to a few log units below the HM buffer) and can have a strong affect on mafic phase composition. Ilmenite–magnetite, quartz–ulvospinel–ilmenite–fayalite (QUILF), annite–sanidine–magnetite, biotite–almandine–muscovite–magnetite (BAMM), and titanite–magnetite–quartz (TMQ) are equilibria providing a basis for the calculation of .Granite barometry plays a critical part in constraining tectonic history. Metaluminous granites offer a range of barometers including ferrosilite–fayalite–quartz, garnet–plagioclase–hornblende–quartz and Al-in-hornblende. The latter barometer remains at the developmental stage, but has potential when the effects of temperature are considered. Likewise, peraluminous granites often contain mineral assemblages that enable pressure determinations, including garnet–biotite–muscovite–plagioclase and muscovite–biotite–alkali–feldspar–quartz. Limiting pressures can be obtained from the presence of magmatic epidote and, for low-Ca pegmatites or aplites, the presence of subsolvus versus hypersolvus alkali feldspars.As with all barometers, the influence of temperature, , and choice of activity model are critical factors. Foremost is the fact that batholiths are not static features. Mineral compositions imperfectly record conditions acquired during ascent and over a range of temperature and pressure and great care must be taken in properly quantifying intensive parameters.