Chemie Der Erde-Geochemistry最新文献

The crystal growth history of an Au-rich sedimentary pyrite nodule from the Timmins-Porcupine Au camp, Ontario, Canada, has been investigated using Electron Backscattered Diffraction and Laser Ablation Inductively Coupled Plasma Mass Spectrometry techniques to study the crystallographic processes controlling metal deportment in the pyrite structure. Results show four distinct growth stages characterized by different pyrite microstructures, crystal forms and trace element compositions. A direct link is observed between the growth of octahedral facets in pyrite and the development of primary (non-tectonic) subgrain boundaries. Furthermore, zones with a high abundance of subgrain boundaries have the highest Au, As, Ag and Cu (and other metals) contents – suggesting metal distribution is linked to the development of microstructures. Finer-grained aggregates are characterized by higher grain boundary density than in coarse areas, making higher trace element concentrations inversely proportional to grain size. Our results indicate that the high Au concentrations (~100 ppm) in pyrite represent a primary feature related to nodule growth, instead of secondary enrichment processes, and highlight the possibility that sediment-hosted pyrite nodules could represent a metal-rich geochemical reservoir for the formation of younger orogenic Au deposits.

The Poularies igneous complex is a Neoarchean (2728 Ma) intrusion composed of diorite, quartz diorite, hornblende tonalite, and biotite tonalite. It is was emplaced into the shallow crust of the Abitibi granite-greenstone belt during volcanic cycle 1 (2730–2725 Ma) and is contemporaneous with the eruption of mafic (Stoughton-Roquemaure Group) and silicic volcanic rocks (Hunter Mine Group). The petrogenetic relationship between the silicic rocks of the Poularies igneous complex is not constrained. In this study we test the petrological association between the different rock types of the Poularies complex using fractional crystallization modeling. Hydrous (H₂O = 3 wt%) fractional crystallization modeling using a ‘primitive’ intermediate starting composition demonstrates that all rock types of the Poularies complex can be generated from a common parental magma in the upper crust (1 kbar) under mildly oxidizing conditions (ΔFMQ = 0). Moreover, it is demonstrated that the parental magma of the Poularies complex was likely derived by partial melting of mafic rocks from the Abitibi granite-greenstone belt. We conclude that the Poularies complex is representative of a magma chamber that generated the silicic lavas of the spatially associated Hunter Mine Group in a rifting or tensional plate stress environment. Our model may be applicable to other shallow syn-volcanic plutons of the Abitibi granite-greenstone belt.

The Ngaye inlier of the Adamawa Yadé Domain is located in the Central African Fold Belt, adjacent to the Nyong Complex at the northern margin of the Congo craton, in central Cameroon. This area consists of metamorphosed granite-greenstone associations comprising amphibole- and pyroxene-rich banded iron formations (BIFs), amphibolites, and migmatitic gneisses. This study reports detailed petrographic, whole-rock geochemical, and LA-ICP-MS U-Pb zircon data for the Ngaye BIFs and associated amphibolites to better constrain their source, tectonic setting, and age. Amphibole-rich BIFs exhibit high REE-Y content and uncommon LREE-enriched patterns. In contrast, pyroxene-rich BIFs display combined low REE-Y content, seawater-like patterns, and positive Eu anomalies, suggesting a mixture of seawater and hydrothermal fluids during their deposition. The geochemical data of associated amphibolites suggest a back-arc setting for the Ngaye metavolcanosedimentary sequence, similar to that of the Nyong Complex. LA-ICP-MS U-Pb zircon dating of amphibole-rich BIFs indicate a maximum depositional age of ca. 2186 Ma and subsequent metamorphism at ca. 2038 Ma, overlapping with that of metavolcanosedimentary sequences from the Nyong Complex. Neoproterozoic age of ca. 598 Ma obtained for these BIFs is interpreted as the Pan-African metamorphic/hydrothermal imprint. This finding suggests that the post-depositional fluid overprint was probably related to the regional Pan-African tectono-thermal event.

Leaching experiments were performed on zinnwaldite-rich greisen, pure zinnwaldite separated from the greisen, spodumene pegmatite, and pure lepidolite in dilute sulfuric, acetic, and oxalic acids (all 0.01 M) as well as deionized water to simulate common environmental conditions. The experiments were carried out at room temperature over a period of 267 days (9 months). Considerable amounts of Li, Al, and Fe (up to 0.76 mM, 6.60 mM, and 0.87 mM, respectively) were observed in the leachates as a result of Li-mica dissolution. The dissolution time-series trends of [SiO₂], [Al] and [Li] for the whole-rock zinnwaldite-greisen and the pure zinnwaldite separate are nearly identical, suggesting preferential dissolution of zinnwaldite in the greisen host rock. Lepidolite released the highest amounts of SiO₂ and Al into the solution, but it also has the smallest grain size and largest specific surface area of the studied samples. Lepidolite samples further show decreasing [Li] in the sulfuric and acetic acid leachates. Spodumene pegmatite released the smallest amounts of analytes in each experiment, except for Fe. Using SEM-EDX, backscattered electron images, and powder XRD, we observed and identified precipitates of secondary quartz resulting from Li-mica dissolution, as predicted by our geochemical modeling. Even though elpasolite was not observed using the SEM, the mineral was detected in some samples via XRD, suggesting that large amounts of F were present in these leachates. We conclude that enhanced weathering of Li-mica deposits due to their development and mining may lead to a considerable influx of Li, Al, and F into surface waters in adjacent areas.

The highly fractured Jurassic carbonates at Jbel Tirremi in northeastern Morocco host fluorite-baryte deposit. The mineralization occurs both as stratabound in marl-limestone contact and as fault-hosted veins (N-S- and NNW-SSE). The mineral paragenesis consists of two fluorite and baryte generations and calcite with subordinate amounts of quartz, dolomite, traces of sulfides (chalcopyrite, pyrite, galena), and oxidized minerals. Fluid inclusion data reveal that hot moderately saline fluids derived from the Paleozoic basement mixed with Triassic brines and cooler, meteoric waters. The REY inventory, C-O-S-Pb-Sr-Nd isotope, and crush-leach data point to the Paleozoic basement as the primary source of metals with a contribution from the Triassic red beds. The refined ore genetic model developed in this study from our new geological and geochemical data includes the downward movement of Triassic-Jurassic evaporated seawaters along normal faults, followed by the leaching of metals from Paleozoic and Triassic rocks, and the subsequent upward flow of these metalliferous fluids. During the Late Cretaceous-Paleocene basin inversion, the deep-seated ore-forming fluids migrated upward, which eventually mixed with Triassic brines and cooler meteoric waters. This fluid mixing caused the precipitation of multiple generations of fluorite and baryte.

Granites are widespread in many Precambrian orogenic belts worldwide; therefore, they can provide insights into orogenic processes and associated magmatism. Zircon UPb age, monazite Th-U-total Pb age and whole-rock geochemical data for a granite pluton from the Gari-Gombo area in the Adamawa-Yade domain of the Central African Fold Belt (CAFB) in East Cameroon are presented. The granite is composed dominantly of perthitic K-feldspars, quartz, plagioclase and minor biotite with accessory monazite, apatite and zircon. LA-ICP-MS zircon UPb dating yielded an age at ca 631–620 Ma, which is interpreted as age of emplacement that coincides with the onset of D2 Pan-African deformation. Monazite grains in Gari-Gombo granite follow strictly the huttonite substitution trend in Th + U vs Si coordinates. Monazites give consistent Neoproterozoic ages of 630 ± 4 Ma and 602 ± 4 Ma, indicating that growth history and crystallization age of monazites also correlate well with the Pan-African plutonism and granulite facies metamorphism (ca 614–600 Ma) in the Gari-Gombo area. The Gari-Gombo pluton samples show high-K calc-alkaline magnesian, slightly peraluminous signature, high SiO₂ (70.16–78.80 wt%), K₂O (4.39–5.38 wt%), and Rb (165–248 ppm), and low P₂O₅ ≤ 0.01 wt% and Sr (146–222 ppm) contents. They have highly-fractionated REE pattern ((La/Yb)_N = 6.17–148.18), moderately Eu negative anomalies (Eu/Eu* = 0.53–0.93) and the obviously Nb and Ti negative anomalies. These geochemical features suggest that the Gari-Gombo pluton is a highly fractionated I-type granite generated by partial melting of older meta-igneous materials at middle to lower crustal levels. The 2.9 and 0.95 Ga inherited zircon grains identified within the studied granites further confirm the existence of ancient crust in this region.

We report new petrology, mineral chemistry, P–T conditions, and fluid inclusion data on mafic granulites from the Mettupalayam region along the Bhavani Suture Zone, Southern Granulite Terrane, India. Phase equilibria modelling of mafic granulites yielded peak P–T conditions of 780–860 °C and 7.6–10.1 kbar followed by a near isothermal decompression along a clockwise P–T path. The trapped fluid inclusions in the peak metamorphic minerals display a melting temperature range from −57.4 °C to −56.6 °C, close to the triple-point temperature of pure CO₂. The primary inclusions homogenized at −18.9 °C to +0.2 °C, corresponding to density values of 0.93–1.03 g/cm³. Homogenization of the secondary inclusions occurred within the range from −6.3 to +18.1 °C, corresponding to low CO₂ densities of 0.79–0.96 g/cm³. From the textural characteristics of the high-density primary carbonic fluid inclusions, we interpret these inclusions as the CO₂-rich syn-metamorphic fluid present during the high-grade metamorphism. The secondary fluids characterised by lower densities have undergone re-equilibration during the exhumation stage (decompression) from the peak granulite-facies metamorphism along a clockwise P–T trajectory. This interpretation is consistent with the occurrence of hornblende + plagioclase symplectite around the porphyroblastic garnet, suggesting decompression. We infer that the high-density CO₂ was the dominant syn-metamorphic fluid components present during the granulite-facies metamorphism in the Mettupalayam region. Such carbonic fluids, possibly derived by degassing from carbonates or mantle sources, probably played a significant role in stabilizing high-grade mineral assemblages along this collisional suture zone.

Active volcanic fumaroles are one of the most spectacular natural objects in terms of mineral diversity. The Great Tolbachik Fissure Eruption (GTFE) (Kamchatka) fumaroles are renowned for its exceptional number of mineral species. The total number of minerals that have been reliably identified from this particular locality exceeds 400, which is approximately 6.5 % of all known minerals to date. In this study, we employ a comprehensive approach (bulk chemistry, microprobe analysis, powder X-ray diffraction, HR X-ray computed tomography, and ³⁴S, ¹⁸O, and ⁶⁵Cu isotope measurements) to study the distribution of primary exhalation and secondary mineral assemblages and to reveal the driving factors responsible for the unique mineral diversity in the Yadovitaya fumarole. High oxygen fugacity, the interaction of minerals with atmospheric oxygen and water from seasonal precipitation (leading to abundant hydrated mineral associations), temperature conditions controlling the spatial distribution of mineral-forming components, gas-rock interactions, and basaltic scoria morphology perfect for the crystallization of various minerals are some of the factors revealed. The combination of these factors caused a stepwise mineralization resulting in 12 zones of the Yadovitaya fumarole with characteristic mineral assemblages. The described mineralogy of the Yadovitaya fumarole demonstrates a consistent spatial evolution of fumarolic mineral assemblages that vary in complexity, chemistry, and interaction patterns with the surrounding environment. The examination of mineralogical and geochemical data yields novel insights into the active volcanic systems that are associated with the formation of distinct oxidation-type fumaroles.

The Nanling metallogenic belt (South China) is one of the largest W-Sn polymetallic provinces in the world. The ore bodies are mainly hosted in Triassic-Jurassic granitoids which formed during a complex history of magmatic evolution. Among them, the Laiziling pluton, which forms the northern part of the Xianghualing district, is an example of Sn-polymetallic deposits that underwent multiple Mesozoic episodes. In this study, the first in-situ U-Pb age dating of zircon and cassiterite minerals, trace element, and Lu-Hf isotopic data are reported for Laiziling NYF-type pegmatites. Four types of pegmatites are identified: stock-like pegmatite, vein-type pegmatite, peripheral vein-type pegmatite, and cap/sill-like pegmatite. Zircon LA-ICP-MS U-Pb geochronology of pegmatites yields an age of ~150 Ma, which is consistent with the age of the associated mineralized granitic pluton. Results of cassiterite age dating indicate that the W-Sn mineralization took place at ca. 150 Ma coeval with pegmatite emplacement. Combined with structure and trace element composition, two young ages (i.e., ~130 and 90 Ma) can be identified from pegmatite veins, suggesting that the studied zircon crystals experienced two distinct periods of magmatic-hydrothermal evolution during the Cretaceous (related to Late Yanshanian magmatism). In addition, some zircon grains are obviously enriched in LREE, which is associated with hydrothermal metasomatism. Compared to the narrow range of magmatic zircons, a wide range of inherited zircons (Proterozoic to Paleozoic) are observed in the studied Late Jurassic pegmatite (Pg1 and Pg2b), suggesting that they were incorporated from pre-existing basement rocks during magma ascent and/or emplacement. Furthermore, U-Pb data for 14 disseminated cassiterite grains yield a ²⁰⁶Pb/²³⁸U age of 221.5 ± 4.2 Ma, documenting evidence of cassiterite inheritance during melt ascension from country rocks or representing the initial stage of Sn enrichment. The εHf values of magmatic zircons show negative εHf values from −4.4 to −16.6 and their crustal model ages (T_DM2) vary between 1328 Ma to 2200 Ma, suggesting the parent magma of the Laiziling pegmatites were derived from partial melting of older crustal components (Proterozoic basement in the Cathaysian Block of South China) and the mixing of mantle materials. This study proposes that multi-stage magmatic-hydrothermal events may have occurred not only in the Xianghualing area but also in the whole Nanling Range, and provides fresh insights into the formation processes of rare metal-bearing pegmatites in South China.

Situated in northeastern Hunan Province, the vein-type Pb-Zn orebodies at Taolin are mainly hosted in NE-/NEE-trending faults between Dayunshan-Mufushan pluton and Neoproterozoic metasedimentary rocks of the Lengjiaxi Group. Hydrothermal mineralization can be divided into five stages: (1) coarse-grained quartz stage, (2) quartz-fluorite-base metal stage, (3) quartz-barite-fluorite-base metal stage, (4) pale pink and colorless quartz stage, and (5) fine-grained quartz stage. In this research, fluid inclusions as well as stable (H-O) and noble gas (He-Ar) isotope compositions were performed to uncover the nature, origin, and evolution of the ore-forming fluids, ore precipitation mechanisms, and mineralization process of the Taolin deposit. Four types of fluid inclusions, i.e., liquid-rich two-phase inclusions (LV-type), pure liquid phase inclusions (PL-type), vapor-rich two-phase inclusions (VL-type), and pure vapor phase inclusions (PV-type), were distinguished in sphalerite, quartz, and fluorite. Microthermometric analysis of fluid inclusion assemblages in sphalerite, quartz, and fluorite from different stages indicates that from the Stage 1 to Stage 5, the homogenization temperatures vary between 168 and 211 °C, between 151 and 198 °C, between 131 and 180 °C, between 132 and 164 °C, and between 118 and 138 °C, respectively, whereas the fluid salinities vary from 12.4 to 16.9 wt% NaCl equivalent, from 9.7 to 14.6 wt% NaCl equivalent, from 5.6 to 10.3 wt% NaCl equivalent, from 3.6 to 9.7 wt% NaCl equivalent, and from 0.9 to 3.8 wt% NaCl equivalent, respectively. The H-O isotope data of quartz and the He-Ar isotopic compositions of sulfide crystals suggest that the ore-forming fluids were a mixture of crust-derived magmatic hydrothermal fluid and meteoric water. Fluid mixing and cooling were likely the crucial mechanisms for ore precipitation.