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American Mineralogist

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Institución detectada Período Navegá Descargá Solicitá
No detectada desde feb. 1998 / hasta dic. 2023 GeoScienceWorld

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Tipo de recurso:

revistas

ISSN impreso

0003-004X

ISSN electrónico

1945-3027

País de edición

Estados Unidos

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Tabla de contenidos

Heterogeneous and retarded phase transformation of ferrihydrite on montmorillonite surface: the important role of surface interactions

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. No disponible

Periodic and non-periodic stacking in molybdenite (MoS2) revealed by STEM

Yiping Yang; Hongping He; Haiyang Xian; Jiaxin Xi; Xiao Wu; Aiqing Chen; Jianxi Zhu; Huifang XuORCID

<jats:title>Abstract</jats:title> <jats:p>Polytypism is a typical feature of layered minerals with differences only in stacking sequences. There is no obvious “phase” boundary among different polytypes, although the frequency of polytypes occurrence is related to its crystallization environment. In the past decades, X-ray studies of molybdenite specimens from a variety of geological environments have revealed that most molybdenite crystals contain both 2H1 (hexagonal) and 3R (rhombohedral) polytypes. However, the stacking sequences of these molybdenite polytypic intergrowths and their formation mechanism are not well understood. Here, we report stacking faults and domains of long-period polytypes identified by high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) in a molybdenite sample from a carbonatite vein in the Huanglongpu Mo-Pb ore deposit in Qinling orogenic belt, Northern China. Several layers of disordered domains intergrown with ordered 2H1 domain were recognized based on the contrast in HAADF image with one-dimensional lattice fringes. In addition, a 30-layer long-period polytype was unambiguously identified by a STEM image. The stacking sequences of 4-, 6-, and 8-layer disordered domains and the 30-layer long-period polytype were further examined using HRSTEM images at the atomic resolution. A 2H3 polytype with three repetitions was also discovered in the sample. We propose that non-equilibrium conditions related to the fluctuation of fluid composition during crystallization resulted in the oscillation of 2H1 and 3R polytypes and intergrowth of various disordered domains. More broadly, our study demonstrates that HAADF-STEM imaging method may be applicable for studying other disordered layered crystals and twinned minerals.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 997-1006

The effect of halogens (F, Cl) on the near-liquidus crystallinity of a hydrous trachyte melt

Yves FeiselORCID; Jonathan M. Castro; Christoph Helo; Donald B. Dingwell

<jats:title>Abstract</jats:title> <jats:p>The effect of F and Cl on the liquidus temperature of a hydrous (~3.5–4 wt% H2O) trachytic melt (~66 wt% SiO2) at 925 to 990 °C and at 100 MPa has been experimentally investigated. We employed a novel disequilibrium approach involving diffusion couple experiments with the two-diffusion couple end-members differing solely in halogen concentrations. A shift of the liquidus temperature by ~50 °C was observed between a halogen-poor and halogen-enriched melt. Each experiment spanned the entire range of F and Cl concentrations between the two end-member compositions. We determined the halogen concentrations at the transition from crystal-bearing to crystal-free melt. These concentrations correspond to the liquidus halogen concentrations of the melt at each experimental temperature. We demonstrate that there is a limiting halogen concentration (~0.19–0.52 wt% F; ~0.07–0.24 wt% Cl), below which the melt crystallizes spherulitic clinopyroxene during heating to the run temperature. At high temperatures, upon diffusion of F and Cl into the halogen-poor melt, those crystals dissolve, leaving behind a dissolution front parallel to the diffusion interface. We propose that the dissolution is a consequence of F and Cl complexing with some of the main cationic components of clinopyroxene (Mg, Fe, Ca), thereby destabilizing this phase. Thus, the experimental dissolution of clinopyroxene is a manifestation of a liquidus depression caused by increased halogen content. Our results show that the liquidus shifts at a rate of ~1575(379) K/mol% of F and Cl in the melt, which is a minimum estimate, assuming both halogens equally drive dissolution. This liquidus depression is valid for a range of halogen concentrations (~0.06–0.87 wt% F; ~0.06–0.36 wt% Cl) and the experimental temperatures. Our findings illustrate that the degassing of halogens during or prior to an eruption can enhance crystallization in the melt and therefore influence magma physical properties that may ultimately affect eruption style.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1007-1017

Occurrence of tuite and ahrensite in Zagami and their significance for shock-histories recorded in martian meteorites

Lixin GuORCID; Sen Hu; Mahesh Anand; Xu Tang; Jianglong Ji; Bin Zhang; Nian Wang; Yangting Lin

<jats:title>Abstract</jats:title> <jats:p>We report on the discovery of two high-pressure minerals, tuite and ahrensite, located in two small shock-induced melt pockets (SIMP 1 and 2) in the Zagami martian meteorite, coexisting with granular and acicular stishovite and seifertite. Tuite identified in this study has two formation pathways: decomposition of apatite and transformation of merrillite under high-P-T conditions. Chlorine-bearing products, presumably derived from the decomposition of apatite, are concentrated along the grain boundaries of tuite grains. Nanocrystalline ahrensite in the pyroxene clast in SIMP 2 is likely to be a decomposition product of pigeonite under high-P-T conditions by a solid-state transformation mechanism. The pressure and temperature conditions estimated from the high-pressure minerals in the shock-induced melt pockets are ~12–22 GPa and ~1100–1500 °C, respectively, although previous estimates of peak shock pressure are higher. This discrepancy probably represents the shift of kinetic relative to thermodynamic phase boundaries, in particular the comparatively small region that we examine here, rather than a principal disagreement between the peak shock conditions.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1018-1029

Zolenskyite, FeCr2S4, a new sulfide mineral from the Indarch meteorite

Chi MaORCID; Alan E. Rubin

<jats:title>Abstract</jats:title> <jats:p>Zolenskyite (IMA 2020-070), FeCr2S4, is a new sulfide mineral that occurs within troilite, with clinoenstatite and tridymite, in the matrix of the Indarch meteorite, an EH4 enstatite chondrite. The mean chemical composition of zolenskyite determined by electron probe microanalysis, is (wt%) S 43.85, Cr 35.53, Fe 18.94, Mn 0.68, Ca 0.13, total 99.13, yielding an empirical formula of Fe0.99Mn0.04Ca0.01Cr1.99S3.98. The ideal formula is FeCr2S4. Electron backscatter diffraction shows that zolenskyite has the C2/m CrNb2Se4-Cr3S4-type structure of synthetic FeCr2S4, which has a = 12.84(1) Å, b = 3.44(1) Å, c = 5.94(1) Å, β = 117(1)°, V = 234(6) Å3, and Z = 2. The calculated density using the measured composition is 4.09 g/cm3. Zolenskyite is a monoclinic polymorph of daubréelite. It may be a high-pressure phase, formed from daubréelite at high pressures (several gigapascals) and moderate temperatures in highly shocked regions of the EH parent asteroid before becoming incorporated into Indarch via impact mixing. Zolenskyite survived moderate annealing of the Indarch whole-rock. The new mineral is named in honor of Michael E. Zolensky, an esteemed cosmochemist and mineralo-gist at NASA’s Johnson Space Center, for his contributions to research on extraterrestrial materials, including enstatite chondrites.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1030-1033

Refined estimation of Li in mica by a machine learning method

Lu Wang; Cheng Su; Luo-Qi Wang; J ZhangZhouORCID; Qun-Ke XiaORCID; Qin-Yan WangORCID

<jats:title>Abstract</jats:title> <jats:p>Li-rich micas are crucial in the exploration for and exploitation of Li resources. The determination of Li in mica using classical bulk chemical methods or in situ microanalytical techniques is expensive and time-consuming and has stringent requirements for the quality of micas and reference materials. Although simple linear and nonlinear empirical equations have been proposed, they are inconsistent with the complex physicochemical mechanisms of Li incorporation and commonly lead to large errors. In this study, we introduce a refined method of multivariate polynomial regression using a machine learning algorithm to estimate Li from multiple major oxide abundances. The performance of our regression model is evaluated using the coefficient of determination (R2) and the root-mean-square error (RMSE) of the independent test sets. The best-performed models show R2 of 0.95 and a RMSE of 0.35 wt% for the test set of data set 1 (all compiled data, n = 2124) and R2 of 0.96 and a RMSE of 0.22 wt% for the test set of data set 2 (only data obtained using in situ techniques, n = 1386). Our results indicate that integration of electron probe microanalysis and multivariate polynomial regression (based on data set 1) presents a robust and convenient approach to quantify Li contents in micas. The application of the proposed approach to micas from central Inner Mongolia, NE China, suggests that in addition to the Weilasituo ore bodies, the Jiabusi granite and greisen and the Shihuiyao metamorphic sediment formation have good potential for Li exploration. Our study also provides preliminary constraints on the genesis of Li deposits.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1034-1044

Olivine in picrites from continental flood basalt provinces classified using machine learning

Lilu Cheng; Yu Wang; Zongfeng YangORCID

<jats:title>Abstract</jats:title> <jats:p>Picrites, dominantly composed of highly forsteritic olivine, can serve as important constraints on primary magma composition and eruption dynamic processes in global continental flood basalt (CFB) provinces. Picrites are commonly divided into high-Ti and low-Ti groups based on whole-rock TiO2 content or Ti/Y ratio. Here, we use an artificial neural network (ANN) to classify the individual olivine in picrites from global CFB provinces according to whether their parental magma is high-Ti or low-Ti to better understand the primary origin and magmatic processes. After training the ANN on 1000 olivine major element compositions data points, the network was able to differentiate chemical patterns for high-Ti and low-Ti olivine and classify olivine into correct types with an accuracy of &amp;gt;95%. Moreover, we find that two types of olivine mix in some single samples from Etendeka, Emeishan, and Karoo CFB provinces. Combining the results with chemical markers of source lithology, we suggest that the two types of olivine originate from two different sources and their olivine populations mixed during the ascent. This mixing then makes the spatial and temporal variation of picrites types in some CFB provinces unclear.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1045-1052

The glass transition and the non-Arrhenian viscosity of carbonate melts

Donald B. Dingwell; Kai-Uwe HessORCID; Martin C. Wilding; Richard A. Brooker; Danilo Di Genova; James W.E. Drewitt; Mark Wilson; Daniel Weidendorfer

<jats:title>Abstract</jats:title> <jats:p>We report the first calorimetric observation of the glass transition for a carbonate melt. A carbonate glass [55K2CO3–45MgCO3 (molar)] was quenched from 780 °C at 0.1 GPa. The activation energy of structural relaxation close to the glass transition was derived through a series of thermal treatments comprising excursions across the glass transition at different heating rates. Viscosities just above the glass transition temperature were obtained by applying a shift factor to the calorimetric results. These viscosity measurements (in the range of 109 Pa·s) at supercooled temperatures (ca. 230 °C) dramatically extend the temperature range of data for carbonates, which were previously restricted to super-liquidus viscosities well below 1 Pa·s. Combining our calorimetrically derived results with published alkaline-earth carbonate melt viscosities at high temperatures yields a highly non-Arrhenian viscosity-temperature relationship and confirms that carbonate liquids are “fragile.” Based on simulations, fragile behavior is also exhibited by Na2CO3 melt. In both cases, the fragility presumably relates to the formation of temperature-dependent low-dimensional structures and Vogel-Fulcher-Tammann (VFT) curves adequately describe the viscosity-temperature relationships of carbonate melts below 1000 °C.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1053-1064

Etching of fission tracks in monazite: Further evidence from optical and focused ion beam scanning electron microscopy

Sean JonesORCID; Barry Kohn; Andy GleadowORCID

<jats:title>Abstract</jats:title> <jats:p>A series of experiments on monazites from Victoria, Australia, is presented to further understand their fission track etching properties. Using a 6 M HCl etchant at 90 °C, SEM images on crystal (100) pinacoid faces reveal well-etched rhombic spontaneous fission track openings. Average rhombic etch pit diameters Dpc and Dpb, parallel to the crystallographic c- and b-axes are 0.81 ± 0.20 µm and 0.73 ± 0.26 µm, respectively. An angular distribution experiment on (100) faces found that spontaneous fission tracks initially etch anisotropically, being preferentially revealed at an azimuth of 90° to the crystallographic c-axis up to ~60 min of etching. As etching continues, however, the distribution becomes progressively more uniform and is essentially isotropic by 90 min. Two experimental methods determined the rate at which the etchant penetrated along the lengths of implanted 252Cf fission tracks. This involved the application of a focused ion beam scanning electron microscope (FIB-SEM) to mill progressively into slightly etched monazite crystals followed by an etch-anneal-etch approach. Results indicate that at least the greater part of the etchable ranges of the latent fission tracks were penetrated by the 6 M HCl etchant within the first few minutes. Continued etching to 5 min indicates that track etching slows down toward the ends of the tracks, but the maximum ranges are estimated to be reached after 5–15 min, which represents the longest time the latent segments of the tracks are exposed to potential annealing at the etchant temperature. Taking into account that implanted 252Cf fission tracks in monazite anneal on average ~4% of their length at 90 °C after 1 h (Jones et al. 2019), suggests that a much shorter duration for exposure to this temperature causes less than ~1% of fission track length reduction during etching.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1065-1073

The low-temperature shift of antigorite dehydration in the presence of sodium chloride: In situ diffraction study up to 3 GPa and 700 °C

Anna Yu Likhacheva; Sergey V. Rashchenko; Anna I. Semerikova; Alexandr V. Romanenko; Konstantin Glazyrin; Oleg G. Safonov

<jats:title>Abstract</jats:title> <jats:p>The dehydration of serpentine mineral antigorite, Mg2.8Si2O5(OH)3.6, is regarded as the key step in metamorphic transformation of ultramafic hydrated rocks in subduction zones, which affects seismicity and feeds volcanic activity. The abundance of alkali-chloride brines derived from deep subduction/upper mantle sources implies the possibility of a large control of the H2O activity by the dissolved salts. The present study examines the effect of alkali chlorides, lowering the H2O activity in fluid, on antigorite stability at high pressure. The decomposition of natural antigorite (Ural) in the presence of a halite-saturated NaCl-H2O fluid was studied up to 3 GPa and 700 °C by in situ X-ray diffraction combined with resistively heated diamond-anvil cell. Reference experiments were also performed on salt-free sample. At 1.5–3 GPa in the presence of halite-saturated fluid (XNaCl ≈ 0.15), antigorite decomposes to an intermediate product assemblage of talc+forsterite at about 550 °C, which is ≈150 °C lower compared to salt-free H2O-unsaturated system. Such a low-temperature shift supports the previous models of a broadened P-T area of serpentinite dehydration in the subducting slab. In addition, the present experiments reveal active dissolution of the product Mg silicates, first of all forsterite, in the NaCl-H2O fluid at 600–700 °C/1.5–3 GPa. This implies that dehydrated serpentinites are a potential source of fluids enriched in MgO and SiO2, which play an important role in deep metasomatic processes.</jats:p>

Palabras clave: Geochemistry and Petrology; Geophysics.

Pp. 1074-1079