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Trace element concentrations and ratios in zircon provide important indicators of the petrological processes that operate in igneous and metamorphic systems. In granitoids, the compositions of zircon have been linked to the behaviour of garnet and plagioclase—pressure-sensitive minerals—in the source during partial melting. This has led to the proposal that Europium anomalies in detrital zircon are linked to the depth of crustal melting or magmatic differentiation and are a proxy for average crustal thickness. In addition to the mineral assemblage present during partial melting, Eu anomalies in zircon are also sensitive to redox conditions as well as magma evolution during extraction, ascent, and emplacement. Here we quantitatively model how rock type, mineral assemblages, redox changes, and reaction sequences influence Eu anomalies of zircon in equilibrium with silicate melt. Partial melting of metasedimentary rocks and metabasites yields felsic to intermediate melts with a large range of Eu anomalies, which do not correlate simply with pressure (i.e. depth) of melting. Europium anomalies of zircon associated with partial melting of metasedimentary rocks are most sensitive to temperature whereas Eu anomalies associated with metabasite melting are controlled by plagioclase proportion—a function of pressure, temperature, and rock composition—as well as changes in oxygen fugacity. Furthermore, magmatic crystallization of granitoids can increase or decrease Eu anomalies in zircon from those of the initial (anatectic) melt. Therefore, Eu anomalies in zircon should not be used as a proxy for the crustal thickness or depth of melting but can be used to track the complex processes of metamorphism, partial melting, and magmatic differentiation in modern and ancient systems. Secular changes of Eu/Eu* from the zircon archive may reflect a change in thermal gradients of crustal melting or an increase in the reworking of sedimentary rocks over time.
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High-pressure, halogen-bearing melt preserved in ultrahigh-temperature felsic granulites of the Central Maine Terrane, Connecticut (U.S.A.)
Abstract Inclusions of relic high-pressure melts provide crucial information on the fate of crustal rocks in the deep roots of orogens during collision and crustal thickening, including at extreme temperature conditions exceeding 1000 °C. However, discoveries of high-pressure melt inclusions are still a relative rarity among case studies of inclusions in metamorphic minerals. Here we present the results of experimental and microchemical investigations of nanogranitoids in garnets from the felsic granulites of the Central Maine Terrane (Connecticut, U.S.A.). Their successful experimental re-homogenization at ~2 GPa confirms that they originally were trapped portions of deep melts and makes them the first direct evidence of high pressure during peak metamorphism and melting for these felsic granulites. The trapped melt has a hydrous, granitic, and peraluminous character typical of crustal melts from metapelites. This melt is higher in mafic components (FeO and MgO) than most of the nanogranitoids investigated previously, likely the result of the extreme melting temperatures—well above 1000 °C. This is the first natural evidence of the positive correlation between temperature and mafic character of the melt; a trend previously supported only by experimental evidence. Moreover, it poses a severe caveat against the common assumption that partial melts from metasediments at depth are always leucogranitic in composition. NanoSIMS measurement on re-homogenized inclusions show significant amounts of CO2, Cl, and F. Halogen abundance in the melt is considered to be a proxy for the presence of brines (strongly saline fluids) at depth. Brines are known to shift the melting temperatures of the system toward higher values and may have been responsible for delaying melt production via biotite dehydration melting until these rocks reached extreme temperatures of more than 1000 °C, rather than 800–850 °C as commonly observed for these reactions.
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- Award ID(s):
- 1753553
- PAR ID:
- 10315244
- Date Published:
- Journal Name:
- American Mineralogist
- Volume:
- 106
- Issue:
- 8
- ISSN:
- 0003-004X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.2138/am-2021-7690
