Garnet Content Research Articles

The eastward intrusion of the Lena River into the East Siberian Sea since the early Holocene

The sedimentary environments and material sources of the eastern and northeastern Lena Delta differ in coarse-grained components and garnet geochemistry, particularly in the Buor-Khaya Bay, where the material composition is primarily influenced by the Lena River, while the Yana Bay sediment is controlled by the Yana River. Analysis of detrital minerals in core LV83–32-3, located in northern Yana Bay, indicates dominant primarily fluvial input from the Yana River, with secondary contributions from the Lena River and minor inputs from coastal permafrost erosion since the early Holocene. During the sea-level rise period from 8.5 to 5 ka, four significant fluvial discharge events from the Yana River were identified, marked by high mica contents, associated with multiple climate warming events. From ∼5 to 1.6 ka, an increasing Lena River runoff transported coastal permafrost material via river flow or river ice, evident in a gradual rise in plagioclase content. After 1.6 ka, a sharp decrease in hypersthene and garnet contents suggests reduced Lena River discharge, coinciding with a similar decline in hypersthene content in the core of the East Siberian Sea since 1.8 ka. Two prominent Lena River fluvial events, dated to 7.1 and 3.7 ka, are identified by the event layers containing minerals typical of the Lena River, rich in hypersthene, garnet and zircon, along with substantial coarse-grained debris such as quartz, plagioclase, siderite and clayey tubes. These two events are also recorded in the East Siberian Sea. The 7.1 ka discharge event may coincide with the separation of the New Siberian Islands from the mainland, while the 3.7 ka event represents a widely distributed Lena River floodplain event.

The maximal chromium content in harzburgitic garnet: an experimental study at P-T conditions of the Earth's upper mantle

The maximal chromium content in harzburgitic garnet: an experimental study at P-T conditions of the Earth's upper mantle

Geochemistry of garnet and scheelite as indicators for skarn-type Mo-W mineralization: A case study from the Shibaogou deposit, Qinling Orogen, China

To understand the mechanism of skarn-type Mo-W mineralization, it is crucial to study fluid evolution. In-situ elemental analysis was conducted on garnet and scheelite from the Shibaogou deposit, a representative large-scale skarn Mo-W deposit in Luanchuan orefield, Qinling orogen, aiming to constrain the origin and evolution of ore-forming fluid and to analyze the skarn mineralization process. Multiple generations of garnet and scheelite were observed along with the multistage of skarnization. I. Anhydrous skarn stage, three generations of garnet (Grt-c, Grt-m, Grt-r) with molybdenite (Mo-I) occurring around Grt-r and scheelite occurring in coarse-grained (primary Sch-I, altered rim Sch-Ia). II. Hydrous skarn stage, minor scheelite (Sch-II) coexisted with actinolite. III. Oxide stage, scheelite (Sch-III) occurred in feldspar-fluorite veins, with minor molybdenite (Mo-II). IV. Quartz sulfide stage, early quartz-molybdenite (Mo-III) veins and later quartz Fe-Zn-Pb-sulfide veins occurred with a few scheelites (Sch-IV). V. Carbonite stage.The Y/Ho ratios of garnet and scheelite indicate that the ore-forming fluid was originally magmatic-hydrothermal. The variations in U and Sn contents of garnet indicate a gradual increase in oxidation state during the anhydrous skarn stage. The high andradite proportion in Grt-m resulted from an increased pH of the fluid, related to the presence of Ca(HCO3)2. This increased pH and Ca2+ activity of fluid led to the main tungsten mineralization (Sch-I). The subordinate Mo mineralization formed at the end of stage I, as the expansion of the molybdenite logfO2-pH stability field, controlled by the decrease in temperature. The redox state evolutions indicated by the consistent Mo contents and (EuN vs. EuN*) of scheelite, with the highest oxidation state occurring in the hydrous skarn stage. The oxidation state reached the lowest level in the sulfide stage with sufficient reduced sulfur, leading to main Mo mineralization. The REE patterns, Nb, and ∑REE contents of scheelite suggest a change in fluid composition to F enrichment after anhydrous skarn, which enhanced the fluid’s ability to dissolve W. In the oxide stage, scheelite formed a second significant mineralization with fluorite: H3WO4F2– + 2Ca2+ = CaWO4 + CaF2 + 3H+. The carbonate wall rocks played a controlling role in the evolution of ore-forming fluid and mineralization mechanism through the fluid-rock interactions.

Composite Separators with Very High Garnet Content for Solid‐State Batteries

AbstractLithium‐metal solid‐state batteries are attractive as next generation of Li‐ion batteries due to higher safety and potentially higher energy density. To improve processability, solid‐composite separators combine advantages of inorganic and polymer separators in hybrid structure. We report a systematic approach to fabricate composite separators with high content (90–95 wt %) of ceramic Li‐ion conducting Li6.45Al0.05La3Zr1.6Ta0.4O12 (LLZO) powder embedded in a polyethylene oxide (PEO)‐LiTFSI (20 : 1) matrix and understand factors affecting their properties and performance. Separators with good mechanical flexibility and excellent thermal stability were obtained, by optimizing materials and processing parameters. It was found that PEO molecular weight strongly influences the microstructure and electrochemical properties of the separators. In optimized separator with 90 wt % of LLZO and PEO with Mw 300,000 g/mol, a total ionic conductivity of 1.4×10−5 S/cm at 60 °C was achieved. The ceramic‐rich separator showed excellent long‐term cycling stability for more than 460 cycles (1000 h) at 0.1 mA/cm2 in Li/Li symmetrical cells and achieved a critical current density of 0.25 mA/cm2. The separators also enabled initial discharge capacities of more than 160 mAh/g in full cells with Li metal anode and composite solid‐state LiNi0.6Co0.2Mn0.2O2 cathode, although rapid capacity fade was observed after 10 cycles in fully solid‐state configuration.

Mineralogy of the Martian mantle inferred from bulk chemical compositions

AbstractUnderstanding the mineralogy of the Martian mantle is essential for constructing geochemical and geophysical models of Mars. This study employs the pMELTS program to determine the mineralogy at the solidus from 11 published bulk silicate Mars (BSM) compositions, within a pressure range of 2–5 GPa. The pMELTS results align with experimental data and calculations from another thermodynamic program (Perple_X/stx11). Mineral modes from compositional models based on Martian meteorite geochemistry show relatively consistent abundances modes (olivine: 48–56 wt%, orthopyroxene: 20–25 wt%, clinopyroxene: 15–17 wt%, garnet: 6–9 wt%). In contrast, mineral modes from compositional models that are not based on Martian meteorite geochemistry exhibit a wider range of olivine and garnet abundances. Additionally, we constrained the mineral modes of the Martian mantle using trace element partitioning and partial melting models. Our calculations indicate that melts derived from mantle sources with a hypothesized garnet content of 5–10 wt% closely match the analyzed compositions of shergottites, validating the garnet mode (6–9 wt%) constrained in our pMELTS calculations. Extracting low‐degree (<4 wt%) melts from a BSM to form depleted Martian mantle (DMM) does not significantly alter the mineralogical modes of solid residues, but it does lead to substantial trace elemental depletion in the DMM. Therefore, enriched, intermediate, and depleted shergottite sources are likely characterized by similar mineral modes yet differ in incompatible element abundances.

Metasomatism in the Precambrian Crust of the Siberian Craton: Results of a Study of Garnet(±orthopyroxene)-biotite-feldspar Xenolith Rocks From Yubileinaya and Sytykanskaya Kimberlite Pipes, Yakutia

Xenoliths in kimberlites are the most perspective objects for studying the composition and structure of the lower levels of the continental crust. Present work is aimed at estimation of P-T fluid conditions of metamorphism for garnet-biotite-feldspar and orthopyroxene-garnet-biotite-feldspar rocks represented as xenoliths in kimberlites of the Yubileynaya and Sytykanskaya pipes, Yakutian kimberlite province. Seven studied samples show inverse dependences of relative contents of garnet and orthopyroxene, orthopyroxene and biotite, garnet and plagioclase, plagioclase and potassium feldspar. This indicates a consistent series of transformations of the assemblage garnet + plagioclase + orthopyroxene ± quartz to the assemblage garnet + biotite + potassium feldspar. In this process, the replacement of plagioclase by potassium feldspar was the leading reaction. Now it is represented by specific reaction textures in the rocks, negative correlations of the mineral contents, as well as in petrochemical characteristics of the rocks. Modeling of xenolith mineral assemblages using the pseudosection approach (PERPLE_X) revealed two groups of rocks corresponding to different depth levels of the Siberian cratonic crust. For rocks where orthopyroxene is absent or is present as single relics, pressure estimates are 9.5–10 kbar, and it is 6–7 kbar for orthopyroxene-bearing samples. The xenolith rocks have close metamorphic peak temperatures of 750–800°C. They experienced 200–250°C cooling and 3–4 kbar decompression, regardless of the level of the crust at which they were initially located. This points to the metamorphic evolution of the rocks during their exhumation, probably associated with collisional processes during the amalgamation of individual terrains of the Siberian craton. Xenoliths enriched in K-feldspar might have been products of metamorphic reactions with participation of aqueous-(carbonic)-salt fluids, which were sourced from basaltic magmas in the lower crust. The most metasomatized rocks were located closest to the place of accumulation of crystallizing magmas.

Ferric Iron in Eclogitic Garnet and Clinopyroxene from the V. Grib Kimberlite Pipe (NW Russia): Evidence of a Highly Oxidized Subducted Slab

Abstract Estimates of oxygen fugacity of eclogitic rocks are linked to the redox evolution of the oceanic protolith during subduction and its residence in the lithospheric mantle, and, based on knowledge of pressures and temperatures, allow modelling of the speciation of volatile elements and diamond (or graphite) versus carbonate stability. To date, the oxygen fugacity of mantle eclogites has been shown to vary between −6 (Kasai, Congo and Udachnaya, Siberia) and −0.1 (Udachnaya, Siberia) log units (relative to the fayalite–magnetite–quartz buffer, FMQ), linked to the low Fe3+ contents of garnets. In this study, we investigated the Fe oxidation state of coexisting garnet and clinopyroxene hand-picked out of 17 diamond-free high-MgO and low-MgO mantle eclogites (dated at 2.84 Ga) from the Grib kimberlite pipe (East-European platform). Measured Fe3+/∑Fe values range between 0.03 and 0.19 for garnet and 0.18–0.38 for clinopyroxene, the former being higher than what was measured previously in garnets equilibrated at mantle conditions. The Fe3+/∑Fe of the reconstructed bulk rock ranges between 0.10 and 0.15 for high-MgO eclogites and 0.10 and 0.24 for low-MgO eclogites (with uncertainties of ± 0.02 and ± 0.03 in both cases). Thermobarometric calculations result in equilibration pressures and temperatures of 3.0–5.2 (± 0.4) GPa and 720–1050 (± 60) °C for both high-MgO and low-MgO eclogites, slightly lower than previous P–T estimates of mantle eclogites from the Udachnaya kimberlite pipe (Siberian craton). At these conditions, ∆logfo2 (FMQ) calculated using the available oxythermobarometric model varies from −1.7 to −0.6 log units for high-MgO eclogites and from −2.9 to 0.9 log units for low-MgO eclogites. Samples recording ∆logfo2 (FMQ) ≤ −1 log units overlap with North Slave, West Africa and Udachnaya eclogites, with no difference among eclogite types. The average values of −1.2 (± 0.4) log units for high-MgO and −0.6 (± 1.1) log units for low-MgO eclogites suggest different redox conditions of basaltic protoliths during subduction worldwide. Previous geochemical studies on the same rock samples reported evidence of cryptic metasomatism in both garnet and clinopyroxene that we demonstrate being not recorded by their major elements, while modal metasomatism evidenced by the presence of phlogopite as a product of interaction with a kimberlitic melt only affects the MgO of the bulk rock. Therefore, we suggest that high Fe3+/∑Fe ratios for garnet (> 0.10) and for reconstructed bulk rocks in the case of both low-MgO and high-MgO samples cannot be due to metasomatic interaction with an oxidized fluid, but rather are the consequence of Fe3+ redistribution in an unusually oxidized mafic protolith upon metamorphism. Our results highlight the redox variability of eclogites of Archaean age at conditions more oxidized than present-day mid-ocean ridge basalts (MORBs) and imply an oxidizing nature of the convective mantle source where magma was formed with consequent speciation of C in the form of carbonate fluid explaining, therefore, the lack of eclogitic diamonds in V. Grib kimberlite pipe.

Garnet geochemistry reveals late-stage oxidation of tin-bearing fractionated granite

In hydrothermal tin (Sn) systems, it remains unclear whether cassiterite precipitates from reduced or oxidized fluids. To resolve this issue, the geochemistry of magmatic garnet and cassiterite separated from fractionated muscovite-garnet granite in the Paleocene Bawapin SnW deposit was systematically investigated. CaO contents in Mn-rich garnet (spessartine) decrease from core to rim in single crystals and are negatively correlated with MnO/(MnO + FeO) ratios. These features suggest that garnet CaO content may be a good differentiation index for granitic magma evolution. Moreover, the Sn content in Mn-rich garnet increases with increasing Ca content and then decreases sharply at Ca contents of approximately 4300 ppm. Combined with evidence of Ta-rich magmatic cassiterite, the decreasing Sn content likely reflects the crystallization of magmatic cassiterite from the more evolved Sn-rich melts under oxidized conditions (ƒO2 > ΔFMQ +1.5), in contrast to the reduced characteristics of the less-fractionated biotite monzogranite (ƒO2 = ΔFMQ - 0.5). Late-stage oxidation might be attributable to fluid exsolution in the water-rich and Fe-poor granitic melts. This further indicates that hydrothermal cassiterite could precipitate in exsolved Sn4+-bearing fluids without Sn oxidation. This conclusion may provide a new perspective to our understanding of granite-related hydrothermal Sn systems worldwide.

Sedimentary record of Variscan unroofing of the Bohemian Massif

The Bohemian Massif in the eastern Variscan Orogen is the host of globally significant ultrahigh-pressure metamorphic rock suites that experienced enigmatic unroofing processes. In the eastern Bohemian Massif, the Moravosilesian Culm Basin (The Czech Republic) with ≤7.5 km thick Lower Carboniferous siliciclastic turbidities has recorded crustal unroofing associated with the late Paleozoic amalgamation of Gondwana and Laurussia. This study presents data from sandstone petrography, heavy mineral assemblages, and detrital zircon U-Pb geochronology from Moravosilesian Culm sediments. Sandstone modal compositions imply continental/recycled orogen affinities. High-grade metamorphic lithic fragments and high garnet contents in upper Culm sediments indicate the exhumation of the middle to lower crustal materials, consistent with those of the Bohemian Massif. Detrital zircon U-Pb data constrain maximum depositional ages of sediments in the Drahany Upland to 335–326 Ma (late Viséan–middle Serpukhovian). Detrital, igneous and metamorphic zircon U-Pb data compiled from surrounding regions support that source regions for lower Culm sediments (Moldanubian Unit and Sudetes) remained the same. Whereas, upper Myslejovice sediments might have derived from exhumation and erosion of the root of the Moldanubian Unit and/or Moravosilesian Nappes. Rapid exhumation of the Moldanubian Unit within the Bohemian Massif during the deposition of upper Culm sediments is inferred.

The onshore West Baram Delta deposits: Provenance and drainage in the Middle Miocene to Pliocene in NW Borneo and comparison to the Champion Delta

The Baram Delta province in NW Borneo forms a major hydrocarbon reservoir offshore northern Sarawak and Brunei. The delta sequence is thereby subdivided into the West Baram delta to the south and the Champion delta to the north. Onshore are the remains of the Neogene delta deposits exposed and provide the possibility to study the equivalent offshore successions in outcrop. This study focuses on the Neogene West Baram delta successions which were studied for sedimentological facies and provenance characteristics. The successions consist of the Lambir, Miri, Tukau, and the enigmatic southern Lambir/Belait-Sarawak formations. Deposition took place in various mixed-energy delta environments between the Langhian and early Pliocene. The sediments are all quartz-rich and heavy minerals are dominated by ultra-stable zircon, rutile and tourmaline. Dominant detrital zircon age clusters are in the Early Cretaceous and Permian-Triassic. Based on light mineral petrography, heavy mineral assemblages, and detrital zircon U–Pb geochronology, all formations are interpreted as derived from multi-recycled sources, likely the underlying Paleogene Rajang Group turbidites and the Oligocene to Lower Miocene Nyalau-Tatau delta deposits. Additionally, literature data of the Champion Delta and one sample from Labuan analysed for provenance in this study are used to demonstrate that the Champion Delta can be distinguished from the West Baram Delta by having higher chrome spinel and garnet contents and slightly different detrital zircon age populations. The Champion Delta deposits are interpreted as sourced by recycling of the Crocker Formation and older turbidites (e.g., Sapulut Formation) with potentially input from ultra-mafic basement rocks of Sabah.

The geochemistry and geochronology of garnet from the Jinchanghe Fe-Cu-Pb-Zn deposit, Baoshan Block, western Yunnan

The Jinchanghe polymetallic Fe-Cu-Pb-Zn deposit is located in the northern region of the Baoshan Block in western Yunnan. Using electron probe micro-analysis and laser ablation inductively coupled plasma mass spectrometry, we analyzed the major, trace, and rare earth elemental contents of garnets from the Jinchanghe deposit. Moreover, U-Pb dating was performed using the laser ablation sector field inductively coupled plasma mass spectrometry (LA-SF-ICP-MS) method to determine the direct mineralization age of the Jinchanghe deposit. Petrographic analyses revealed three garnet generations: early (GrtI), middle (GrtII), and late (GrtIII). GrtI (And55.69-64.47Gro30.28-41.21Ura + Pyr + Spe + Alm2.35-5.49) was characterized by irregular shapes and weak optical properties, and primarily comprised Fe-rich grossular. GrtII (And53.69-96.17Gro2.78-45.07Ura + Pyr + Spe + Alm0.59-2.12) was characterized by andradite, in which GrtIIa was a homogeneous body, whereas GrtIIb shows exhibited oscillatory zoning with abnormal interference colors. Fine-veined andradite aggregates were predominant in GrtIII (And70.51-90.33Gro6.34-27.80Ura + Pyr + Spe + Alm1.03-3.32). The GrtI, GrtIIa, and the rims of GrtIIb were depleted in heavy rare earth elements and enriched in light rare earth elements, with positive Eu anomalies, indicating that these garnets crystallized from mildly acidic magmatic hydrothermal fluids. However, the cores of GrtIIb had negative Eu anomalies and may have crystallized from a relatively neutral Cl-rich fluid. GrtIII was severely depleted in light rare earth elements with positive Eu anomalies, indicating the presence of a weakly acidic environment. Accordingly, owing to a decrease in temperature and an increase in oxygen fugacity, the pH of the Jinchanghe deposit may have transitioned from an early weakly acidic to neutral, then to a late weakly acidic environment. Furthermore, the ages of GrtII and GrtIII ranged from 520 to 496 Ma, which places the formation of the Jinchanghe deposit during the Late Cambrian. The deposit is closely related to the arc magmatic rocks produced by the subduction of the Proto-Tethys Ocean.

Sound velocity of eclogite at high pressures and implications for detecting eclogitization in subduction zones

The increased velocity associated with decaying seismicity in the subducting oceanic crust usually has been attributed to its eclogitization. However, the degree of the eclogitization of subducting oceanic crust at depth remains unclear due to the lack of velocity data for eclogite at pressures of >3 GPa. In this study, the P- and S-wave velocities of eclogite aggregates composed of omphacite and garnet (Omp100, Omp80Grt20, and Omp50Grt50) were measured simultaneously at pressures of up to 8 GPa using ultrasonic interferometry. The velocities of the eclogite aggregates increased with rising pressure and garnet content. By determining the velocities at different pressures using the finite strain equation, the elastic moduli of the eclogites and their pressure derivatives were determined to be KS0 = 119−134 GPa, KS0′ = 5.2−5.3, G0 = 73−80 GPa, and G0′ = 1.5−1.6. The high-wave velocity and low VP/VS ratio of the eclogites, combined with the seismic tomography and seismicity distribution, jointly constrain the depth and composition of eclogitization in the subducted oceanic crust of Northeast Japan, and a new 1-D velocity structure is proposed. We also compiled and calculated the depth of the eclogitization and the garnet content of the subducting oceanic crusts in 27 typical locations around the Pacific Ocean. The depth of the eclogitization was positively correlated with the age of the subduction zone, and the garnet content was estimated to be 12%−32% in our model.

OH incorporation and retention in eclogite-facies garnets from the Zermatt–Saas area (Switzerland) and their contribution to the deep water cycle

Abstract. The incorporation mechanisms of OH groups in garnet were investigated in a suite of high-pressure rocks from the Zermatt–Saas area (Switzerland) using a combination of Fourier transform infrared spectroscopy (FTIR) and electron probe micro-analysis (EPMA). Investigated garnet specimens include grossular–andradite–uvarovite solid solutions in serpentinite and rodingite and almandine–grossular–pyrope–spessartine solid solutions in eclogite, mafic fels and meta-sediment. All rocks experienced the same peak metamorphic conditions corresponding to a burial depth of ∼ 80 km (∼ 540 ∘C, 2.3 GPa), allowing determination of the OH content in garnet as a function of rock type. The capacity for OH incorporation into garnet strongly depends on its composition. Andradite-rich (400–5000 µg g−1 H2O) and grossular-rich garnet (200–1800 µg g−1 H2O) contain at least 1 order of magnitude more H2O than almandine-rich garnet (< 120 µg g−1 H2O). Microscale analyses using FTIR and EPMA profiles and maps reveal the preservation of OH zoning throughout the metamorphic history of the samples. The OH content correlates strongly with Mn, Ca and Ti zoning and produces distinct absorption bands that are characteristic of multiple nano-scale OH environments. The use of 2D diffusion modelling suggests that H diffusion rates in these rocks is as low as log(D[m2 s−1]) = −24.5 at 540 ∘C. Data were collected for the main garnet-bearing rock types of the Zermatt–Saas area allowing a mass balance model of H2O to be calculated. The result shows that ∼ 3360 kg H2O km−1 (section of oceanic crust) yr−1 could be transported by garnet in the subducting slab beyond 80 km depth and contributed to the deep-Earth water cycle during the Eocene subduction of the Piemonte–Liguria Ocean.

Geochemical Characteristics of Garnet from Zinc–Copper Ore Bodies in the Changpo–Tongkeng Deposit and Its Geological Significance

The Changpo–Tongkeng tin polymetallic deposit in Dachang, Guangxi, is a world-class, superlarge, polymetallic tin deposit consisting of lower skarn zinc–copper ore bodies and upper tin polymetallic ore bodies. Garnet is the main gangue mineral in the skarn zinc–copper ore bodies and has a granular texture. Based on hand specimens and microscopic observations, the existing garnet can be divided into two generations: an early generation (Grt I) and a late generation (Grt II). The results of electron probe microanalysis (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) in situ microanalysis show that the contents of SiO2 and CaO in the garnets from the two generations present limited variations, while the FeOT and Al2O3 contents vary significantly, indicating the grossular–andradite solid solution series (Gro29–82And12–69). Compared with Grt I (Gro72And25), Grt II (Gro39And59) is Fe-enriched and oscillatory zoning is developed. The total rare earth element (REE) contents in the two generations of garnet are relatively low, showing light rare earth element (LREE) depletion and heavy rare earth element (HREE) enrichment patterns. Grt II has higher REE content than Grt I and exhibits significant negative Eu anomalies (δEu = 0.18–0.44). The contents and variation characteristics of the major and trace elements in the two generations of garnet suggest that there were variable redox conditions and water/rock ratios in the hydrothermal system during the crystallization process of garnet. In the early stage, skarnization was in a relatively closed and low-oxygen fugacity system, with hydrothermal diffusion metasomatism being dominant, forming homogeneous Grt I lacking well-developed zoning. In the late stage of skarnization, the oxygen fugacity of the ore-forming fluids increased, with infiltration metasomatism being dominant, forming Grt II with well-developed oscillatory zoning. The contents of Sn, As, W, In, and Ge in the garnets are relatively high and increase with the proportion of andradite. Sn in zinc–copper ore bodies mainly exists in the form of isomorphic substitution in garnet, which may be the main reason for the lack of tin ore bodies during the skarn stage. This paper compares the trace element contents in garnets from domestic skarn deposits. The results indicate that the Sn content and δEu in garnet can be used to evaluate the tin-forming potential of skarn deposits.

Intra‐Seasonal Variability in Sediment Provenance and Transport Processes in the Brahmaputra Basin

AbstractSediment composition in modern fluvial settings is commonly assessed regarding spatial but rarely temporal variability, potentially leading to a bias of unknown extent. Here, we present the grain‐size distribution, bulk chemical and mineralogical composition of a time‐series set of 36 suspended sediment samples from the Brahmaputra river, as well as clay and heavy mineral analysis of selected samples. Sampling covers the June–November 2021 period, which included two major flooding events. We show that the two flooding events are characterized by contrasting grain size, with the first event characterized by a grain‐size minimum and the second by a grain‐size maximum. Although grain sizes of the first flood and the period after the second are similar, their compositions differ significantly, highlighted by a factor‐two decrease of biotite largely compensated by an increase in quartz. By contrast, the content of garnet, clinopyroxene, sillimanite, and rutile increased compared to epidote and amphibole during the second flood event. By relating the results to spatio‐temporal rainfall and discharge patterns and basin morphology, we conclude that the first flooding primarily mobilized hydraulically pre‐sorted sediments from the exposed sandbars of the floodplains, while those sandbars are already submerged during the second flooding in a single‐channel system, resulting in higher sediment contributions from highland tributaries draining igneous and high‐grade metamorphic rocks. Such temporal variations pose constraints on the interpretation of compositional differences between individual samples regarding sediment provenance and dispersal and should be considered in studies of modern drainage basins as well as ancient sediment routing systems.

Metamorphic P-T paths and zircon U-Pb ages of Paleoproterozoic metabasic dykes in the Jiapigou area, South Jilin Province: Implications for the tectonic evolution of the North China Craton

The distribution and tectonic evolution of the Paleoproterozoic orogenic belts in the North China Craton (NCC) remain controversial. Especially, the extent of the Paleoproterozoic magmatic and metamorphic influences on the Archean Longgang Block needs further demonstration. This paper presents detailed petrographic and mineralogical analyses, phase equilibria modeling and zircon dating for three metabasic dyke samples in the Jiapigou area, South Jilin Province, in order to discuss their metamorphic evolution and tectonic implications. Petrographic observation and phase modeling using THERMOCALC suggest that these metabasic dykes have experienced the metamorphism with clockwise P-T paths under low-amphibolite facies, high-amphibolite facies and high-pressure granulite facies. Their peak P-T conditions were constrained to be 0.6–0.9 GPa/580–650 °C (JN1929), ∼0.95 GPa/757 °C (JN1918) and ∼1.15 GPa / 820 °C (JN1932), according to the stability fields of mineral assemblage and isopleths of Ti content in amphibole, anorthite component (XAn) in plagioclase, pyrope content (XPy) and grossular content (XGrs) in garnet. The peak conditions correspond to apparent geothermal gradients of 19–22℃/km, being medium-pressure type. Zircon U-Pb dating shows that the metabasic dykes have a protolith crystallization age of 2199 ± 5 Ma (MSWD = 0.43), and a metamorphic age of 1855 ± 41 Ma (MSWD = 0.21). The protolith ages, metamorphic characteristics and ages of the metabasic dykes in South Jilin can be well compared with those for metabasic dykes in East Hebei and North Liaoning, indicating that the northern part of the Longgang Block was extensively affected by the mid Paleoproterozoic magmatism, and was involved in an orogen to be metamorphically reworked during the late Paleoproterozoic (1.82–1.85 Ga). In addition, this orogeny mainly occurred along the northern margin of the craton, which is different from the ∼1.95 Ga orogeny in the NCC.

The Dynamics of Transformation of Lithospheric Mantle Rocks Beneath the Siberian Craton

The problem of heat–mass transfer in the permeable areas above the asthenosphere zones was numerically studied based on an examination of the inclusion content in the minerals (olivine and clinopyroxenes) of igneous and metamorphic rocks of the lithospheric mantle and the Earth’s crust; evaluations of thermodynamic conditions of the inclusion formation; and experimental modeling of the influence of hot reduced gases on rocks in the mantle beneath the Siberian craton. The flow of fluids of a certain composition from the upper-mantle magma chambers leads to the formation of zonal metasomatic columns in the ultrabasic mantle lithosphere in the permeable zones of deep faults (starting from the lithosphere base at 6–7 GPa). When petrogenic components enter from the magma pocket, depleted ultrabasic lithospheric mantle rocks change to substrates, which can be considered as the deep counterparts of crustal rodingites. Other fluid compositions result in strong calcination and pronounced salinization of the metasomatized substrates or an increase in the garnet content of the primary ultrabasic matrix. A region of alkaline rocks forms above these areas, which changes to pyroxenes, amphiboles, and biotites. The heat–mass transfer modeling for the two-velocity hydrodynamic model shows that gas–fluid and melt percolation lead to an increase in the thermal front velocity under convective heating and a pressure drop in flow. It is also shown that grospidites are considered to be eclogites, are found in the permeable zones of the lithospheric mantle columns serving as conduits for the melt/fluids and represent the products of the carbonated metasomatic columns. The carbonization caused by proto-kimberlite melts may essentially decrease the diamond grade of kimberlites due to carbon oxidation.

Ultrahigh-Temperature Mafic Granulites in the Rauer Group, East Antarctica: Evidence from Conventional Thermobarometry, Phase Equilibria Modeling, and Rare Earth Element Thermometry

AbstractThe Rauer Group in East Antarctica is a typical high- to ultrahigh-temperature (HT–UHT) granulite-facies terrane. As UHT metamorphism has been recognized only in Mg–Al-rich pelitic granulites from the Mather Paragneiss, the regional extent of UHT metamorphism remains uncertain, which has hindered our understanding of the genesis and tectonic setting of UHT metamorphism in the Rauer Group. In this study, representative samples of mafic granulite were selected from Archean crustal domains to constrain the peak metamorphic conditions and P–T path and to assess the regional extent of UHT metamorphism in the Rauer Group. Integrated results from mineral reaction histories, thermobarometry, and phase equilibria modeling indicate a multi-stage clockwise P–T evolution for mafic granulites involving pre-peak compression, heating to UHT peak conditions, post-peak near-isothermal decompression under UHT conditions, and subsequent decompressional cooling. The pre-peak prograde history is based mainly on the inclusion assemblage of clinopyroxene + plagioclase + amphibole + quartz + ilmenite ± orthopyroxene ± k-feldspar within porphyroblastic garnet and clinopyroxene and records the transformation from a quartz-present to quartz-absent system. The UHT peak conditions are well constrained at 930°C–1030°C and 10.6–12.8 kbar on the basis of the stability field of the observed peak assemblage of (orthopyroxene–quartz)-free garnet + clinopyroxene + plagioclase + amphibole + ilmenite + melt, as well as measured mineral compositions, including the high Ti content in amphibole (Ti = 0.38–0.42 p.f.u.), the anorthite content of coarse-grained plagioclase cores (XAn = 0.35–0.42), and the grossular content in garnet (XGrs = ~0.21) in P–T pseudosections. The peak T conditions are consistent with thermometric estimates in the range of 930°C–1030°C obtained from garnet–clinopyroxene, garnet–orthopyroxene, and Ti-in-amphibole thermometers, and are slightly lower than estimates (1020°C–1120°C) obtained from thermometers based on rare earth elements. The near-isothermal decompression under UHT conditions can be divided into two stages. The early stage is recorded by coronae of orthopyroxene + plagioclase around clinopyroxene and core–mantle/rim anorthite-increasing zoning in plagioclase. The late stage is identified from symplectites of orthopyroxene + plagioclase ± amphibole around porphyroblastic garnet, which were formed at the expense of garnet at 915°C–950°C and 7.6–8.2 kbar as inferred from the amphibole–plagioclase thermometer. The subsequent decompressional cooling to fluid-absent solidus conditions (~875°C and ~6.5 kbar) is indicated by the growth of biotite, which formed at the expense of symplectic minerals, reflecting back-reaction of melt with symplectite minerals. The peak UHT metamorphic conditions and clockwise P–T path of the studied mafic granulites from the Archean crustal domains are similar to those of Mg–Al-rich pelitic UHT granulites from the Mather Paragneiss. The UHT conditions recorded by the mafic granulites, combined with previously identified isolated UHT localities in the Rauer Group, imply that UHT metamorphism in the Rauer Group occurred over a much wider region than previously thought and probably extends over the whole Archean crustal domain. Our findings have general significance in understanding the regional extent of other UHT granulite-facies terranes worldwide.

The Effect of the Garnet Content on Deformation Mechanisms and Weakening of Eclogite: Insights From Deformation Experiments and Numerical Simulations

AbstractWe performed deformation experiments on omphacite‐garnet aggregates at a temperature of 1000°C, a confining pressure of 2.5 GPa, and a strain rate of 3 × 10−6 s−1 and complemented them by numerical simulations to gain insight into the role of garnet fraction for the deformation behavior of dry eclogite, with a focus on strain weakening mechanisms. We determined the spatial and temporal evolution of strain and strain rate by basing numerical simulations on experimentally derived microstructures, and thereby identified characteristic deformation mechanisms. Pure omphacite and garnet aggregates deform by two different mechanisms. Internally strained clasts and low‐angle grain boundaries indicate crystal plasticity for omphacitite; the fracture dominated fabric of garnetite documents brittle deformation. Electron channeling contrast imaging, however, revealed low‐angle grain boundaries and free dislocations in garnet crystals, suggesting that minor crystal plasticity accompanies the brittle failure. Eclogitic aggregates show varying deformation behavior between the two end‐members shifting from crystal plastic toward brittle deformation with increasing garnet content. All samples exhibit strain weakening. The intensity of weakening shows a positive correlation with the garnet content. Our combined experimental, numerical, and microstructural investigations suggest that the majority of strain weakening is associated with crystal plastic processes in omphacite. Numerical simulations and experiments show that a garnet content above 25% enhances the activity of crystal plastic processes in omphacite and results in strain localization, which subsequently weakens the eclogite.

The Phosphorus Budget of the Silicate Earth Based on an Updated Estimate of the P/Nd Ratio

AbstractCalculating the phosphorus (P) budget of the bulk silicate Earth (BSE) is necessary to understand the global P cycle and the origin and evolution of life. Covariations of P and neodymium (Nd) contents suggest that P is 1.1–1.4 times more incompatible than Nd during mantle melting and magmatic differentiation. As such, the P/Nd ratios of mantle sources can be estimated using inverse modeling, and the P budget of the BSE can be calculated from the P/Nd ratios of the continental crust, mid‐ocean ridge basalts (MORBs), and ocean island basalts (OIBs). The P/Nd ratios for the MORB and OIB mantle sources and continental crust are 62.5 ± 0.8 (2σm), 57.0 ± 0.5 (2σm), and 28.4 ± 12.0 (2σm), respectively. These reservoirs have different P/Nd ratios due to subduction, magmatic differentiation, and mineralogy. Subduction can significantly affect the global P and Nd cycles. Magmatic differentiation, especially in the continental crust, may redistribute P by changing the contents of garnet, apatite, and other minerals. The fractional contributions of these global reservoirs suggest the modern BSE has a P/Nd ratio of 57.7 ± 3.0 (2σm), equating to ∼3.1 × 1020 kg of P in the BSE.