A simple and robust method for calculating temperatures of granitoid magmas

Calculating the temperatures of magmas from which granitoid rocks solidify is a key task of studying their petrogenesis, but few geothermometers are satisfactory. Zircon saturation thermometry has been the most widely used because it is conceptually simple and practically convenient, and because it is based on experimental calibrations with significant correlation of the calculated zircon saturation temperature (TZr) with zirconium (Zr) content in the granitic melt (i.e., TZr ∝ ZrMELT). However, application of this thermometry to natural rocks can be misleading, resulting in the calculated TZr having no geological significance. This thermometry requires Zr content and a compound bulk compositional parameter M of the melt as input variables. As the Zr and M information of the melt is not available, petrologists simply use bulk-rock Zr content (ZrBULK-ROCK) and M to calculate TZr. In the experimental calibration, TZr shows no correlation with M, thus the calculated TZr is only a function of ZrMELT. Because granitoid rocks represent cumulates or mixtures of melt with crystals before magma solidification and because significant amount Zr in the bulk-rock sample reside in zircon crystals of varying origin (liquidus, captured or inherited crystals) with unknown modal abundance, ZrBULK-ROCK cannot be equated with ZrMELT that is unknown. Hence, the calculated magma temperatures TZr using ZrBULK-ROCK have no significance in both theory and practice. As an alternative, we propose to use the empirical equation $$T_{SiO_{2}}$$ T S i O 2 (°C) = -14.16 × SiO2 + 1723 for granitoid studies, not to rely on exact values for individual samples but focus on the similarities and differences between samples and sample suites for comparison. This simple and robust thermometry is based on experimentally determined phase equilibria with T ∝ 1/SiO2.

Trace-Element Geochemistry of Sulfides in Upper Mantle Lherzolite Xenoliths from East Antarctica

Sulfides in upper mantle lherzolite xenoliths from Cretaceous alkaline-ultramafic rocks in the Jetty Peninsula (East Antarctica) were studied for their major and trace-element compositions using SEM and LA-ICP-MS applied in situ. Modal abundance of sulfides is the lowest in Cpx-poor lherzolites ≤ Spl-Grt lherzolites << Cpx-rich lherzolites. Most sulfides are either interstitial (i-type) or inclusions in rock-forming minerals (e-type) with minor sulfide phases mostly present in metasomatic veinlets and carbonate-silicate interstitial patches (m-type). The main sulfide assemblage is pentlandite + chalcopyrite ± pyrrhotite; minor sulfides are polydymite, millerite, violarite, siegenite, and monosulfide solution (mss). Sulfide assemblages in the xenolith matrix are a product of the subsolidus re-equilibration of primary mss at temperatures below ≤300 °C. Platinum group elements (PGE) abundances suggest that most e-type sulfides are the residues of melting processes and that the i-type sulfides are crystallization products of sulfide-bearing fluids/liquids. The m-type sulfides might have resulted from low-temperature metasomatism by percolating sulfide-carbonate-silicate fluids/melts. The PGE in sulfide record processes are related to partial melting in mantle and intramantle melt migration. Most other trace elements initially partitioned into interstitial sulfide liquid and later metasomatically re-enriched residual sulfides overprinting their primary signatures. The extent of element partitioning into sulfide liquids depends on P, T, fO2, and host peridotite composition.

Magnetite Redistribution during Multi-stage Serpentinization: Evidence from the Taishir massif, the Khantaishir Ophiolite, Western Mongolia

&lt;p&gt;Magnetite commonly forms during serpentinization of mantle peridotite, involving the hydrogen generation within the oceanic lithosphere. Although magnetite is concentrated in veins, the mobility of iron during serpentinization is still poorly understood. The completely serpentinized ultramafic rocks (originally dunite) within the Taishir massif in the Khantaishir ophiolite, western Mongolia, include abundant magnetite + antigorite veins, which manifest novel distribution of magnetite. The serpentinite records the multi-stage serpentinization, in order of (1) Al-rich antigorite + lizardite mixture with hourglass texture (Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; = 0.46-0.69 wt%; Atg+Lz), (2) Al-poor antigorite composed of thick veins and their branches (Atg), and (3) chrysotile that cut all previous textures. The Mg# (= Mg/ (Mg + Fe&lt;sub&gt;total&lt;/sub&gt;)) of Atg+Lz (0.94-0.96) is lower than Atg (0.99) and chrysotile (0.98). In the region of Atg+Lz, magnetite occurs as the arrays of fine grains (&lt;50 &amp;#956;m) around the hourglass texture. In the Atg veins replacing Atg+Lz, magnetite disappears and re-precipitated as coarse grains (100-250 &amp;#956;m) in the center of some veins. As the extent of replacement of Atg+Lz by Atg veins increases, both modal abundance of magnetite and the bulk Fe content decrease. These characteristics indicate that hydrogen generation mainly occurred at the stage of Atg+Lz formation, and magnetite distribution was largely modified via dissolution and precipitation in response to later fluid infiltration associated with the Atg veins. This also indicates the high iron mobility within the serpentinized peridotites even after the primary stage of magnetite formation.&lt;/p&gt;

Experimental investigation of glaucophane rheology through shear and axial compression Griggs apparatus experiments on hot-pressed aggregates

&lt;p&gt;Constraining the rheological properties of glaucophane is critical to understanding subduction zone rheology. Based on the rock record, glaucophane is a major constituent mineral associated with subducted mafic oceanic crust at blueschist metamorphic facies. No flow law describing the crystal-plastic deformation of this mineral has been developed. Previous experimental work involving glaucophane focused on the deformation of natural polyphase rocks with an emphasis on seismic anisotropy. Here we focus on experiments intended to activate crystal-plastic deformation mechanisms in glaucophane using a monophase aggregate powder separated from natural samples from Syros Island, Greece. We are conducting general shear and axial compression experiments in a Griggs apparatus using temperatures of 600-800&amp;#176;C, pressures of 1 GPa and shear strain rates between 10&lt;sup&gt;-5&lt;/sup&gt;-10&lt;sup&gt;-6&lt;/sup&gt;. Our first experiment was in a general shear orientation at 700&amp;#176;C, 1 GPa, and a shear strain rate of 1.18x10&lt;sup&gt;-5&lt;/sup&gt;. This experiment had a ~80% modal abundance of glaucophane and appears to have been dominated by brittle deformation. After the first experiment, we decided to produce a purer glaucophane aggregate powder containing ~95% glaucophane with ~5% other phases and are finishing mineral separation at the time of submission. We will present early mechanical and microstructural data from experiments with the aim of developing a glaucophane flow law. Our results will also be compared to ongoing experiments focused on the viscous properties of experimentally deformed natural aggregates (see abstract in this conference by Tokle et al.).&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;

Magmatically folded and faulted schlieren zones formed by magma avalanching in the Sonora Pass Intrusive Suite, Sierra Nevada, California

The southwestern margin of the Late Cretaceous Sonora Pass Intrusive Suite, northern Sierra Nevada, California (USA), preserves a densely populated zone of magmatic structures that record dynamic magmatic layer formation and deformation (faulting and folding) within a solidifying upper-crustal magma mush. This zone consists largely of coupled melanocratic (or schlieren) and leucocratic bands hosted within the 95.6 ± 1.5 Ma Kinney Lakes granodiorite (Leopold, 2016), with orientations approximately parallel to the intrusive margin and with inward younging directions. Schlieren consist of a high modal abundance of medium-grained ferromagnesian minerals (hornblende + biotite), zircon, sphene, apatite, opaque minerals, and minor plagioclase and interstitial quartz. Leucocratic bands are dominated by coarse-grained feldspar + quartz with minor ferromagnesian and accessory minerals. Whole-rock geochemical and Sr and Nd isotopic data indicate that the schlieren are derived from the Kinney Lakes granodiorite by effective mechanical separation of mafic minerals and accessory phases. We interpret that the schlieren zone at the margin of the Kinney Lakes granodiorite formed by large-scale collapse of crystal mush by “magma avalanching,” facilitated by gravity, local convection, and possibly by host-rock stoping at the margin. This process eroded a significant portion of the solidifying margin of the chamber and resulted in the formation of magmatically deformed layered structures, which experienced further mingling, re-intrusion, magmatic erosion, and recycling processes. We envisage that magma avalanching of magma mushes in plutons can be achieved by any unstable process (e.g., tectonic, fluid-assisted, stoping, or gravity-driven) in large, long-lived magma-mush chambers.

Detrital zircon geochronology and geochemistry of Jurassic sandstones in the Xiongcun district, southern Lhasa subterrane, Tibet, China: implications for provenance and tectonic setting

Jurassic sandstones in the Xiongcun porphyry copper–gold district, southern Lhasa subterrane, Tibet, China were analysed for petrography, major oxides and trace elements, as well as detrital zircon U–Pb and Hf isotopes, to infer their depositional age, provenance, intensity of source-rock palaeo-weathering and depositional tectonic setting. This new information provides important evidence to constrain the tectonic evolution of the southern Lhasa subterrane during the Late Triassic – Jurassic period. The sandstones are exposed in the lower and upper sections of the Xiongcun Formation. Their average modal abundance (Q21F11L68) classifies them as lithic arenite, which is also supported by geochemical studies. The high chemical index of alteration values (77.19–85.36, mean 79.96) and chemical index of weathering values (86.19–95.59, mean 89.98) of the sandstones imply moderate to intensive weathering of the source rock. Discrimination diagrams based on modal abundance, geochemistry and certain elemental ratios indicate that felsic and intermediate igneous rocks constitute the source rocks, probably with a magmatic arc provenance. The detrital zircon ages (161–243 Ma) and εHf(t) values (+10.5 to +16.2) further constrain the sandstone provenance as subduction-related Triassic–Jurassic felsic and intermediate igneous rocks from the southern Lhasa subterrane. A tectonic discrimination method based on geochemical data of the sandstones, as well as detrital zircon ages from sandstones, reveals that the sandstones were most likely deposited in an oceanic island-arc setting. These results support the hypothesis that the tectonic background of the southern Lhasa subterrane was an oceanic island-arc setting, rather than a continental island-arc setting, during the Late Triassic – Jurassic period.

Portland clinker production with carbonatite waste and tire-derived fuel: crystallochemistry of minor and trace elements

This paper presents results on the composition of Portland clinkers produced with non-conventional raw-materials and fuels, focusing on the distribution of selected trace elements. Clinkers produced with three different fuel compositions were sampled in an industrial plant, where all other parameters were kept unchanged. The fuels have chemical fingerprints, which are sulfur for petroleum coke and zinc for TDF (tire-derived fuel). Presence of carbonatite in the raw materials is indicated by high amounts of strontium and phosphorous. Electron microprobe data was used to determine occupation of structural site of both C3S and C2S, and the distribution of trace elements among clinker phases. Phosphorous occurs in similar proportions in C3S and C2S; while considering its modal abundance, C3S is its main reservoir in the clinker. Sulfur is preferentially partitioned toward C2S compared to C3S. Strontium substitutes for Ca2+ mainly in C2S and in non-silicatic phases, compared to C3S.