scholarly journals Generation of the Mt Kinabalu Granite by Crustal Contamination of Intraplate Magma Modelled by Equilibrated Major Element Assimilation with Fractional Crystallization (EME-AFC)

2019 ◽  
Vol 60 (7) ◽  
pp. 1461-1487 ◽  
Author(s):  
A Burton-Johnson ◽  
C G Macpherson ◽  
C J Ottley ◽  
G M Nowell ◽  
A J Boyce
Keyword(s):  
Oxygen Isotope ◽  
Fractional Crystallization ◽  
Major Element ◽  
Crustal Contamination ◽  
Mafic Magma ◽  
Isotope Ratios ◽  
Geochemical Data ◽  
Magmatic Differentiation ◽  
Clear Trend ◽  
Mount Kinabalu

AbstractNew geochemical data are presented for the composite units of the Mount Kinabalu granitoid intrusion of Borneo and utilised to explore the discrimination between crustal- and mantle-derived granitic magmas. The geochemical data demonstrate that the units making up this composite intrusion became more potassic through time. This was accompanied by an evolution of isotope ratios from a continental-affinity towards a slightly more mantle-affinity (87Sr/86Sri ∼0·7078; 143Nd/144Ndi ∼0·51245; 206Pb/204Pbi ∼18·756 for the oldest unit compared to 87Sr/86Sri ∼0·7065, 143Nd/144Ndi ∼0·51250 and 206Pb/204Pbi ∼18·721 for the younger units). Oxygen isotope ratios (calculated whole-rock δ18O of +6·5–9·3‰) do not show a clear trend with time. The isotopic data indicate that the magma cannot result only from fractional crystallization of a mantle-derived magma. Alkali metal compositions show that crustal anatexis is also an unsuitable process for genesis of the intrusion. The data indicate that the high-K units were generated by fractional crystallization of a primary, mafic magma, followed by assimilation of the partially melted sedimentary overburden. We present a new, Equilibrated Major Element -Assimilation with Fractional Crystallization (EME-AFC) approach for simultaneously modelling the major element, trace element, and radiogenic and oxygen isotope compositions during such magmatic differentiation; addressing the lack of current AFC modelling approaches for felsic, amphibole- or biotite-bearing systems. We propose that Mt Kinabalu was generated through low degree melting of upwelling fertile metasomatized mantle driven by regional crustal extension in the Late Miocene.

A new approach to modelling differentiation (with particular focus on granitic magmatism): Equilibrated Major Element Assimilation with Fractional Crystallisation (EME-AFC)

2020 ◽  
Author(s):  
Alex Burton-Johnson ◽  
Colin Macpherson ◽  
Christopher Ottley ◽  
Geoff Nowell ◽  
Adrian Boyce
Keyword(s):  
Major Element ◽  
Crustal Contamination ◽  
Mafic Magma ◽  
Fractional Crystallisation ◽  
Geochemical Data ◽  
Magmatic Differentiation ◽  
New Approach ◽  
Mount Kinabalu ◽  
High K ◽  
Granitic Magmatism

<p>We present the new approach to AFC modelling published as Editor’s Choice in the July 2019 issue of Journal of Petrology [1].</p><p>Our new, Equilibrated Major Element – Assimilation with Fractional Crystallisation (EME-AFC) approach simultaneously models the major element, trace element, and radiogenic and oxygen isotope compositions during such magmatic differentiation (including a new approach to oxygen modelling); addressing the lack of current AFC modelling approaches for felsic, amphibole- or biotite-bearing systems. We discuss the application of this model to granitic magmatism in SE Asia and Antarctica, with particular focus on the Mt Kinabalu granitic intrusion of Borneo. We discuss the background to the model, and explain how it can be freely accessed via GitHub [2], and applied to other scenarios of magmatic differentiation; not just granitic magmatism.</p><p>We present new geochemical data for the composite units of the Mount Kinabalu, and use this to explore the discrimination between crustal- and mantle-derived granitic magmas. The isotopic data (oxygen, Hf, Sr, Nd, and Pb) indicate that the magma cannot be the result only from fractional crystallisation of a mantle-derived magma. Alkali metal compositions show that crustal anatexis is also an unsuitable processes for genesis of the intrusion. Using the new EME-AFC modelling approach, we show that the high-K pluton was generated by fractional crystallisation of a primary, mafic magma followed by assimilation of the partially melted sedimentary overburden. We propose that Mt Kinabalu was generated through low degree melting of upwelling fertile metasomatised mantle driven by regional crustal extension in the Late Miocene.</p><p>[1] Burton-Johnson, A., Macpherson, C.G., Ottley, C.J., Nowell, G.M., Boyce, A.J., 2019. Generation of the Mt Kinabalu granite by crustal contamination of intraplate magma modelled by Equilibrated Major Element Assimilation with Fractional Crystallisation (EME-AFC). J. Petrol. 60, 1461–1487.</p><p>[2] https://github.com/Alex-Burton-Johnson/EME-AFC-Modelling</p>

A geochemical study of two peraluminous granites from south-central Iberia: the Nisa-Albuquerque and Jalama batholiths

1999 ◽  
Vol 63 (1) ◽  
pp. 85-104 ◽  
Author(s):  
J. A. Ramirez ◽  
L. G. Menendez
Keyword(s):  
Fractional Crystallization ◽  
Magma Mixing ◽  
Geochemical Data ◽  
Magmatic Differentiation ◽  
Peraluminous Granite ◽  
South Central ◽  
Geochemical Study ◽  
Peraluminous Granites ◽  
Magma Pulses ◽  
Fractional Crystallization Process

AbstractIn this paper we present new petrological and geochemical data for two peraluminous granite batholiths (Nisa Alburquerque and Jalama batholiths) representative of the ‘Araya-type’ granites of the Central-Iberian Zone. Both granites are composite with several facies (monzogranites and leucogranites) that can be grouped into two main granite units: the external units and central units. Intrusive relationships and lack of geochemical coherence between the central and external units indicate that they are not comagmatic but represent different pulses. The central units of both batholiths are petrologically and geochemically different. On the other hand, external units show a lot of similarities and are the main object of this study. The main characteristics of the external granites can be interpreted in terms of an incomplete fractional crystallization process of early mineral phases (plg + Kf + bt) which probably took place at the level of emplacement. Other possible mechanisms of magmatic differentiation (magma mixing, restite unmixing, sequential melting) can be discarded based on field, petrography and geochemical data. We propose that the ‘Araya-type’ granites are formed by the intrusion of distinct magma pulses (central and external). Further evolution within each pulse can be due to incomplete fractional crystallization possibly taking place at the emplacement level.

Pétrologie des roches volcaniques de sillon de roches vertes archéennes de Matagami–Chibougamau à l'ouest de Chapais (Abitibi est, Québec), 2. Le groupe hautement potassique d'Opémisca

1986 ◽  
Vol 23 (8) ◽  
pp. 1169-1189 ◽  
Author(s):  
Christian Picard ◽  
Michel Piboule
Keyword(s):  
Fractional Crystallization ◽  
Crustal Contamination ◽  
Major Elements ◽  
Geochemical Data ◽  
Continental Margins ◽  
Garnet Lherzolite ◽  
Calc Alkaline ◽  
Volatile Elements ◽  
High K ◽  
Active Continental Margins

In the western part of the Chapais syncline (Abitibi East, Quebec), the Opemisca Group unconformably overlies the Roy Group at a low angle. It consists of a thick turbidite sequence covered by an interdigitated sequence of lavas and alluvial cone sediments. The subaerial lavas include two sequences evolving from porphyric metabasalts to metatrachyandesites and porphyric metatrachytes (lower sequence) or to K-rich aphanitic meta-andesites (upper sequence). These lavas, with calc-alkaline to shoshonitic affinity, have high K2O, Ba, Sr, and Th contents and show highly enriched LREE spectra.The behaviour of major elements, trace elements, and lanthanides suggests an origin from partial melting of a mantle source consisting of a garnet lherzolite enriched in K, Sr, Rb, Ba, and Th by volatile elements and also by crustal contamination and by fractional crystallization mechanisms. The evolution of the lavas of the lower sequence, progressively deficient in Y, seems to have been controlled by fractional crystallization of a plagioclase, clinopyroxene, and olivine mixture; this was followed for the metatrachyandesites and metatrachytes by high H2O activity of a feldspar, amphibole, titanomagnetite, and apatite mixture. The evolution of lavas enriched in Y in the upper sequence seems to have been controlled by weak H2O activity of the anhydrous plagioclase, clinopyroxene, and olivine assemblage.The petrographic and geochemical data suggest an emplacement similar to that occurring on the active continental margins of the central Andes and implies the existence of a late-stage ensialic arc. [Translated by the journal]

scholarly journals Mantle Melting and Magmatic Processes Under La Picada Stratovolcano (CSVZ, Chile)

2019 ◽  
Vol 60 (5) ◽  
pp. 907-944 ◽  
Author(s):  
Jacqueline Vander Auwera ◽  
Olivier Namur ◽  
Adeline Dutrieux ◽  
Camilla Maya Wilkinson ◽  
Morgan Ganerød ◽  
...  
Keyword(s):  
Fractional Crystallization ◽  
Geochemical Data ◽  
Upper Crust ◽  
Volcanic Zone ◽  
Nazca Plate ◽  
Southern Volcanic Zone ◽  
Magmatic Processes ◽  
Crystal Accumulation ◽  
Primary Magmas ◽  
Differentiation Trend

Abstract Where and how arc magmas are generated and differentiated are still debated and these questions are investigated in the context of part of the Andean arc (Chilean Southern Volcanic Zone) where the continental crust is thin. Results are presented for the La Picada stratovolcano (41°S) that belongs to the Central Southern Volcanic Zone (CSVZ) (38°S–41·5°S, Chile) which results from the subduction of the Nazca plate beneath the western margin of the South American continent. Forty-seven representative samples collected from different units of the volcano define a differentiation trend from basalt to basaltic andesite and dacite (50·9 to 65·6 wt % SiO2). This trend straddles the tholeiitic and calc-alkaline fields and displays a conspicuous compositional Daly Gap between 57·0 and 62·7 wt % SiO2. Interstitial, mostly dacitic, glass pockets extend the trend to 76·0 wt % SiO2. Mineral compositions and geochemical data indicate that differentiation from the basaltic parent magmas to the dacites occurred in the upper crust (∼0·2 GPa) with no sign of an intermediate fractionation stage in the lower crust. However, we have currently no precise constraint on the depth of differentiation from the primary magmas to the basaltic parent magmas. Stalling of the basaltic parent magmas in the upper crust could have been controlled by the occurrence of a major crustal discontinuity, by vapor saturation that induced volatile exsolution resulting in an increase of melt viscosity, or by both processes acting concomitantly. The observed Daly Gap thus results from upper crustal magmatic processes. Samples from both sides of the Daly Gap show contrasting textures: basalts and basaltic andesites, found as lavas, are rich in macrocrysts, whereas dacites, only observed in crosscutting dykes, are very poor in macrocrysts. Moreover, modelling of the fractional crystallization process indicates a total fractionation of 43% to reach the most evolved basaltic andesites. The Daly Gap is thus interpreted as resulting from critical crystallinity that was reached in the basaltic andesites within the main storage region, precluding eruption of more evolved lavas. Some interstitial dacitic melt was extracted from the crystal mush and emplaced as dykes, possibly connected to small dacitic domes, now eroded away. In addition to the overall differentiation trend, the basalts to basaltic andesites display variable MgO, Cr and Ni contents at a given SiO2. Crystal accumulation and high pressure fractionation fail to predict this geochemical variability which is interpreted as resulting from variable extents of fractional crystallization. Geothermobarometry using recalculated primary magmas indicates last equilibration at about 1·3–1·5 GPa and at a temperature higher than the anhydrous peridotite solidus, pointing to a potential role of decompression melting. However, because the basalts are enriched in slab components and H2O compared to N-MORB, wet melting is highly likely.

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