Experimental constraints on amphibole stability in primitive alkaline and calc-alkaline magmas

Equilibrium crystallization experiments were carried out on two primitive basaltic rocks (APR16: Na2O+K2O=4.40 wt%; CM42: Na2O+K2O=2.59 wt%) with the aim to investigate the amphibole stability in the differentiation processes at deep crustal level, of primitive alkaline (APR16) and calc-alkaline (CM42) magmas. The experiments were performed with different initial H2O contents (0-5 wt%), at pressure of 800 MPa, in the temperature range of 975-1225 °C. For the explored conditions, amphibole crystallization occurs in both compositions at H2O in the melt >7wt% while the temperature of their occurrence is lower in the alkaline composition (<1050 °C in APR16 and ≥1050 °C in CM42). Moreover, amphibole crystallization seems to be influenced by the Na2O/K2O ratio rather than the absolute Na2O content in the melt. This is evident when experimental results on the APR16 and CM42 are compared with experimental data obtained from a primitive ultrapotassic composition (leucite-basanite: Na2O+K2O=4.58 wt%) and with thermodynamic modelling by the Rhyolite-MELTS algorithm. The comparison shows that amphibole never saturates the leucite-basanite at any of the investigated/modelled conditions, even when an extended crystallization increases the Na2O of melts up to contents like those of calc-alkaline experimental glasses. We conclude that, at pressure of 800 MPa and hydrous conditions, only primitive liquids with Na2O/K2O ratio ≥0.9 are more prone to crystallize amphibole

Amphibole: A major carrier of helium isotopes in crustal rocks

The first evidence for a specific role of amphiboles in He isotope balance of crustal rocks was presented in early contributions by Gerling et al. (1971, 1976). Since then it was shown that 4He and 3He concentrations in amphiboles generally exceed those in the host rock samples. Recently amphibole was considered as an important carrier of noble gases and other volatiles components in the course of their subduction into the mantle. This paper presents new data on the balance and mobility of noble gas isotopes and major gas constituents in amphibole separates in order to understand sources and evolution of volatile components of 2666 Ma old alkaline granites from Ponoy massif (Kola Peninsula), which underwent metamorphism 1802 Ma ago.In the amphiboles 3He, 4He and 40Ar* were dominantly produced in situ due to radioactive decay of the parent isotopes and associated nuclear reactions. A small fraction of He (≈ 3% of the total) is liberated by crushing and shows 3He/4He ratio indistinguishable from that found by total extraction. The fraction of trapped 40Ar* amounts to ≈ 40%; both these fractions presumably occupy fluid inclusions and show rather low 4He/40Ar* ≈ 0.1, a factor of ≈ 150 below the production ratio (calculated assuming no loss / gain of the species has happened since the time of metamorphism).3He has been better preserved in amphiboles compared with 4He: the retention parameter (measured amount of He / totally produced amount) for 3He (≈ 0.4) exceeds that for 4He (≈ 0.15).He extraction by fast and slow linear heating of amphiboles resulted in different release patterns. The fast heating (within 12 to 40 °C min− 1) revealed a superposition of two peaks. When heating with slower heating rate (below 8 °C min− 1) was applied, the high-temperature peak disappeared (the “disappearing site”). Extractions of He atoms from grain and powder samples at different heating rates have shown that: (1) the “disappearing site” is revealed by the fast heating analyses of different amphibole samples but not only those from the Ponoy massif; (2) amount of He liberated from the “disappearing site” is variable and generally much less than the total amount of He in the sample; (3) analysis of the powder produced in the crushing experiments never reveals the “disappearing site”; the temperature of He release from the powder is lower than that from the mm grain size sample by ≈ 50 °C. Possible explanations of the nature of the “disappearing site” are discussed. However, independently on nature of this effect, repeated gas extractions by heating at different rates would give additional information about structure and its transformation during heating of amphiboles.The simplest explanation of the observed abundances of noble gas isotopes in the amphibole separates from Ponoy granites suggests local production, redistribution and partial loss of noble gases during evolution of the massif

Mineral chemistry of late Variscan gabbros from central Spain: constraints on crystallisation processes and nature of the parental magmas

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Crystal-chemistry and short-range order of fluoro-edenite and fluoro-pargasite: a combined x-ray diffraction and ftir spectroscopic approach

In this study we address the crystal-chemistry of a set of five samples of F-rich amphiboles from the Franklin marble (USA), using a combination of microchemical (EMPA), SREF, and FTIR spectroscopy methods. The EMPA data show that three samples fall into the compositional field of fluoro-edenite whereas two samples are enriched in high-charged C cations, and must be classified as fluoro-pargasite. Mg is by far the dominant C cation, Ca is the dominant B cation (with BNa in the range 0.00-0.05 apfu, atoms per formula unit), and Na is the dominant A cation, with A0 (vacancy) in the range 0.07-0.21 apfu; WF is in the range 1.18-1.46 apfu. SREF data show that: TAl is completely ordered at the T(1) site; the M(1) site is occupied only by divalent cations (Mg and Fe2+); CAl is disordered between the M(2) and M(3) sites; ANa is ordered at the A(m) site, as expected in F-rich compositions. The FTIR spectra show a triplet of intense and sharp components at ~ 3690, 3675, and 3660 cm-1, which are assigned to the amphibole, and the systematic presence of two very broad absorptions at 3560 and 3430 cm-1. These latter are assigned, on the basis of polarized measurements and FPA imaging, to chlorite-type inclusions within the amphibole matrix. Up to eight components can be fitted to the spectra; band assignment based on previous literature on similar compositions shows that CAl is disordered over the M(2) and M(3) sites, thus supporting the SREF conclusions based on the bond distance analysis. The measured frequencies are typical of O-H groups pointing toward Si-O(7)-Al tetrahedral linkages, thus allowing to characterize the SRO (short-range-order) of TAl in the double chain. Accordingly, the spectra show that in the fluoroedenite/pargasite structure, the T cations, Si and Al, are ordered in such a way that Si- O(7)-Si linkages regularly alternate with Si-O(7)-Al linkages along the double chain.Comment: 38 pages, 10 figures - in press. Mineralogical Magazine, special issue for the international year of crystallography (2013) in pres

Archeometric Investigation of the Stone Tools of the Vatya Culture (Pest County, Hungary)

With the analysis of the middle Bronze Age (2000–1350 BC) Vatya culture findings in Pest county (Central Hungary) comprising of more than 400 polished stone tools and instrument tools this is the first archaeometric study with such scale in Hungary. In order to characterize petrographically the raw-material of the stone tools macroscopic and microscopic stone analyses were made together with mineralogical and geochemical analyses. In the course of the work a new digital database the Archaeometric Stone Tool Database was established. Based on the results, the material of the instrument stones is mainly sandstone and quartzite that were easy to collect from their source areas. Local volcanics, mostly amphibole containing andesite variations dominated among the material of the polished stone tools. Ophiolites (metamorphic basic rocks, serpentinized basic and ultrabasic rocks) were the raw-material of stone axes that indicate either more distant travels for raw-material or exchange import

An assessment of the mantle and slab components in the magmas of an oceanic arc volcano: Raoul Volcano, Kermadec arc

Raoul Volcano occupies a simple oceanic subduction setting in the northern part of the Kermadec arc on the Pacific–Australian convergent plate boundary. The primary inputs to the magmatic system that feeds the volcano are a subduction component derived from the subducting old Pacific oceanic lithosphere and its veneer of pelagic sediment, and the overlying peridotitic mantle wedge. Conservative trace elements that are very incompatible during mantle melting are relatively depleted in Raoul lavas indicating a source that has been depleted during an earlier melting event. Major element co-variations indicate magma genesis by 25% near fractional melting of a mantle source that is weakly depleted (2% melt extraction) relative to a fertile MORB source. An important influence on the composition of the mantle component is progressive melt extraction coupled with minimal advection of fresh material into the sub-arc zone followed by melt extraction from a melting column beneath the spreading centre of an adjacent back arc basin. High field strength element and rare earth element systematics indicate involvement of a subduction-related component of constant composition. Two fluid components can be distinguished, one enriched in large ion lithophile elements inferred to be an aqueous fluid that is continuously added to the ascending melt column and the other a less mobile fluid that transfers Th. A homogeneous subduction-related component of constant composition and magnitude arises if the slab-derived flux migrates from the slab–mantle interface to the sub-arc melting column by repeated episodes of amphibole formation and decomposition its composition is then governed by the distribution coefficients of pyroxene and its magnitude by the degree of amphibole saturation of mantle peridotite. The results from Raoul Volcano are comparable to those from other oceanic subduction-related arcs such as South Sandwich and Marianas suggesting that this is a general model for oceanic arcs

Recycling Argon through Metamorphic Reactions: the Record in Symplectites

The 40Ar/39Ar ages of metamorphic micas that crystallized at high temperatures are commonly interpreted as cooling ages, with grains considered to have lost 40Ar via thermally-driven diffusion into the grain boundary network. Recently reported laser-ablation data suggest that the spatial distribution of Ar in metamorphic micas does not always conform to the patterns predicted by diffusion theory and that despite high metamorphic temperatures, argon was not removed efficiently from the local system during metamorphic evolution. In the Western Gneiss Region (WGR), Norway, felsic gneisses preserve microtextural evidence for the breakdown of phengite to biotite and plagioclase symplectites during near isothermal decompression from c. 20–25 to c. 8–12 kbar at ~700°C. These samples provide an ideal natural laboratory to assess whether the complete replacement of one K-bearing mineral by another at high temperatures completely ‘resets’ the Ar clock, or whether there is some inheritance of 40Ar in the neo-crystallized phase. The timing of the high-temperature portion of the WGR metamorphic cycle has been well constrained in previous studies. However, the timing of cooling following the overprint is still much debated. In-situ laser ablation spot dating in phengite, biotite-plagioclase symplectites and coarser, texturally later biotite yielded 40Ar/39Ar ages that span much of the metamorphic cycle. Together these data show that despite residence at temperatures of ~700°C, Ar is not completely removed by diffusive loss or during metamorphic recrystallization. Instead, Ar released during phengite breakdown appears to be partially reincorporated into the newly crystallizing biotite and plagioclase (or is trapped in fluid inclusions in those phases) within a close system. Our data show that the microtextural and petrographic evolution of the sample being dated provides a critical framework in which local 40Ar recycling can be tracked, thus potentially allowing 40Ar/39Ar dates to be linked more accurately to metamorphic history