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Dean C. Presnall

Publications and source records attributed to Dean C. Presnall.

2 recordsLinked to original sources

A mass proportion method for calculating melting reactions and application to melting of model upper mantle lherzolite

We present a method for calculating quantitative melting reactions in systems with multiple solid solutions that accounts for changes in the mass proportions of phases between two points at different temperatures along a melting curve. This method can be applied to any data set that defines the phase proportions along a melting curve. The method yields the net change in mass proportion of all phases for the chosen melting interval, and gives an average reaction for the melting path. Instantaneous melting reactions can be approximated closely by choosing sufficiently small melting intervals. As an application of the method, reactions for melting of model upper mantle peridotite are calculated using data from the system CaO-MgO-Al 2 O 3 -SiO 2 -Na 2 O (CMASN) over the pressure interval 0.7 – 3.5 GPa. Throughout almost this entire pressure range, melting of model lherzolite involves the crystallization of one or more solid phases, and is analogous to melting at a peritectic invariant point. In addition, we show that melting reactions for small melting intervals (< 5%) along the solidus of mantle peridotite are significantly different from those calculated for large melting intervals. For large melting intervals (> 10%), reaction stoichiometries calculated in CMASN are usually in good agreement with those available for melting of natural peridotite. The coefficients of melting reactions calculated from this method can be used in equations that describe the behavior of trace elements during melting. We compare results from near-fractional melting models using (1) melting reactions and rock modes from CMASN, and (2) constant reactions representative of those used in the literature. In modeling trace element abundances in melt, significant differences arise for some elements at low degrees of melting (< 10%). In modeling element abundances in the residue, differences increase with increase in degree of melting. Reactions calculated along the model lherzolite solidus in CMASN are the only ones available at present for small degrees of melting so we recommend them for accurate trace element modeling of natural lherzolite.

Earth and Planetary Science Letters

Fusion Relations in the System NaAlSi3O8-CaAl2Si2O8-KAlSi3O8-SiO2-H2O and Generation of Granitic Magmas in the Sierra Nevada Batholith

Chemical analyses of 167 typical specimens indicate that about 95 percent of the intrusive rocks of the central Sierra Nevada contain more than 79 percent normative Ab + An + Or + Qz. If the composition of the lower continental crust is similar to or slightly more felsic than andesite, as seems likely, the system NaAlSi 3 O 8 -CaAl 2 Si 2 O 8 -KAlSi 3 O 8 -SiO 2 -H 2 O provides an excellent chemical model for testing various schemes of fusion of the lower crust and crystallization of the resulting magmas. From consideration of this system in conjunction with field and petrographic data, we conclude that the intrusive rocks are best explained by repeated episodes of equilibrium fusion corresponding to magmatic sequences defined by field, petrologic, chemical, and geochronologic data. Fractional crystallization of the crystal-liquid mush generated by equilibrium fusion, coupled with periodic upward or lateral movement of the less crystallized central part of the magma, would produce the characteristic mafic to felsic sequence of intrusion; each mafic to felsic sequence corresponds to a separate equilibrium fusion event. In contrast, a close approach to fractional fusion of the lower crust is inadequate for obtaining most of the plutonic rocks, because rock compositions capable of being produced by this process do not match those observed. Normal amounts of conductive heat from the mantle and from radioactive decay in the crust may have been capable of causing fusion in the deepest parts of a thickened crust under the central part of the Sierra Nevada without the aid of a transient heat source from the mantle, but would have been inadequate where the crust was thin in the western Sierra Nevada. However, upward transport of andesitic and basaltic magmas generated along a Mesozoic subduction zone dipping beneath the Sierra Nevada would have provided sufficient additional heat to make fusion of the lower crust unavoidable. This implies that a major portion of the present batholith must have been derived from the lower crust.

California