Garnet Chemistry Research Articles

Evidence for Low‐Pressure Crustal Anatexis During the Northeast Atlantic Break‐Up

AbstractWhile basaltic volcanism is dominant during rifting and continental breakup, felsic magmatism may be a significant component of some rift margins. During International Ocean Discovery Program (IODP) Expedition 396 on the continental margin of Norway, a graphite‐garnet‐cordierite bearing dacitic unit (the Mimir dacite) was recovered in two holes within early Eocene sediments on Mimir High (Site U1570), a marginal high on the Vøring Transform Margin. Here, we present a comprehensive textural, petrological, and geochemical study of the Mimir dacite in order to assess its origin and discuss the geodynamic implications. The major mineral phases (garnet, cordierite, quartz, plagioclase, alkali feldspar) are hosted in a fresh rhyolitic, vesicular, glassy matrix that is locally mingled with sediments. The major element chemistry of garnet and cordierite, the presence of zircon inclusions with inherited cores, and thermobarometric calculations all support an upper crustal metapelitic origin. While most magma‐rich margin models favor crustal anatexis in the lower crust, thermobarometric calculations performed here show that the Mimir dacite was produced at upper‐crustal depths (<5 kbar, 18 km depth) and high temperature (750–800°C) with up to 3 wt% water content. In situ U‐Pb analyses on zircon inclusions give a magmatic crystallization age of 54.6 ± 1.1 Ma, consistent with emplacement that post‐dates the Paleocene‐Eocene Thermal Maximum. Our results suggest that the opening of the Northeast Atlantic was associated with a phase of low‐pressure, high‐temperature crustal anatexis preceding the main phase of magmatism.

Paleozoic to Mesozoic paleotectonic reconstructions of Gondwana assembly: Insights from petrography, heavy mineral chemistry and detrital U–Th–total Pb monazite geochronology of sandstones in the Pranhita-Godavari Basin (SE India)

The provenance study of Paleo-Mesozoic sediments of the Pranhita-Godavari (P-G) Basin, located in the southeastern India is crucial for the reconstruction of the eastern Gondwanaland, including the India-Antarctica connection. This study examines petrography, heavy mineral chemistry and detrital monazite geochronology of the Permo-Carboniferous to Cretaceous, predominantly fluviatile sandstones in the P-G Basin to track the possible sediment sources in East Antarctica and Eastern India. The sandstones show a gradual shift in composition from feldspatho-quartzose to quartzose arenite from older to younger succession, accompanied by a change in source terranes in a changing setting from transitional continental to the cratonic interior. The heavy minerals of the sandstones are dominated by garnet, rutile, ilmenite, monazite and zircon in order of decreasing abundance. The mineral chemistry of garnet and rutile indicates the predominance of sources from amphibolite to granulite facies rocks with minor inputs from metapelitic sources. The increase in textural and mineralogical maturity of sandstones accompanied by a gradual increase in ilmenite alteration from the bottom to the top of the succession indicates the attainment of tectonic stability with time. U–Th–total Pb dating of detrital monazites yielded three distinct major clusters at (1) 2556–2125 Ma, (2) 969–715 Ma, and (3) 581–418 Ma. Based on the correlation of source composition and monazite geochronology and paleocurrent data, the source of sediments is traced to the orogens of the Eastern Ghats mobile belt, East Antarctica (including Rayner and Napier complex), Karimnagar granulite belt, Khammam schist belt, and Bhopalpatnam granulite belt, situated to the west, south, and southeast of the present outcrops of the P-G Gondwana succession. The younger age populations possibly represent the sediment input from Kuunga Orogen, which represents the youngest orogenic event (635–488 Ma) in the Gondwana assembly. The rocks of Kuunga orogeny, occurring to the south of the basin, was a minor contributor to the P-G Gondwana sediments of this basin. The new data supports that the Eastern Ghats Mobile Belt of India and East Antarctica were conjugate to each other till the Late Triassic Period, both of which contributed major sediments to the P-G Gondwana Basin.

О некоторых особенностях региональной поисковой алмазной минералогии

Analysis of the results of carried out investigations of mantle modules in kimberlite diatremes of main diamondiferous regions of the Siberian platform was made. Morphology and chemistry of garnets, chrome-diopsides, clinopyroxenes, picroilmenites, chromites and chrome-spinellids were investigated. Generally, the quantity of diamond association minerals is proportional to diamondiferousness of certain variety of kimberlite for each type of kimberlite rocks composing pipes. It is stated that comprehensive studying of kimberlites and diamond property are very important, because the diamond is a mineral with a broad complex of physical-chemical and crystal-morphological features, reflecting peculiarity of thermodynamic and geochemical conditions of their formation, which can be used as typomorphic indicators. Detailed complex investigations of diamond and its paragenetic accessory minerals allow establishing material-indicative parameters of kimberlite magmatism of various productivity and geologic-structural position of kimberlite bodies, and address issues about primary sources of placer diamonds, as well. Upgrading the line of research on creation of more efficient ore processing flowsheets and providing crystalintegrity technologies, expansion of diamond application areas with consideration of their real structure and physical features, as well as revelation of natural targets with increased quality of diamond raw material, are all related with investigation of primary indicator minerals of kimberlites.

Garnet chemical zoning: a clue for the tectono-metamorphic history of the Proterozoic Mayombe chain (West Congo Belt), Congo-Brazzaville

Abstract The Mayombe chain of Congo is part of the West Congo Belt, which belonged to the western Gondwana supercontinent. It consists of Paleoproterozoic gneisses and schists that are tectonically stacked and overthrust Neoproterozoic low-grade metamorphic rocks. Although Neoproterozoic context of the chain is relatively well established, the tectono-metamorphic evolution of its Paleoproterozoic basement still under discussion. Petrography, garnet chemistry and phase equilibria modelling were used to constrain tectono-metamorphic evolution of meta-plutonic and meta-sedimentary rocks from the Western Domain of the Mayombe chain. Microprobe analysis reveals three garnet types: (i) 2-stage garnets with distinct cores (Grt1) and rims (Grt2), (ii) unzoned garnet showing narrow diffusion zones along cracks and rims and (iii) syn-kinematic garnet with normal growth zoning. These complex and simple features of garnet growth are, respectively, related to a polycyclic evolution linked in this area to: (i) the superposition of Eburnean (c. 2000 Ma) and Pan-African (c. 600 Ma) orogenies and (ii) a monocyclic evolution related to a single Pan-African event taking into account ages of the protoliths. The oldest metamorphic assemblage (Eburnean) is preserved in amphibolite facies conditions marked by the first generation of garnet, whereas the younger (Pan-African) event varies from amphibolite facies in the southwest (4–6 kbar, 550°C–600°C) to greenschist facies in the northeast (4–6 kbar at 450°C–550°C) confirming the westward increase in metamorphic grade during the Pan-African event. Mineral equilibria modelling shows also a relatively HP episode culminated at 11.5–12.5 kbar and 525°C–550°C which tectonic environment stills less understood.

Preliminary data on the mineral chemistry of garnet from the skarn alteration associated with the Elatsite porphyry-copper gold deposit, Bulgaria

The skarn alteration is poorly preserved at the Elatsite, restricted to the hornfelses from the East, Southeast and Southern part of the deposit. The rocks are defined as exoskarns, with a mineral composition including garnets, epidote, pyroxene, amphiboles, carbonates, prehnite, quartz, sulphides. The newly formed minerals occur in poorly preserved layers. The garnet grains are subhedral with inclusions of epidote and quartz, while some of them are corrode with carbonate and zeolites formed in the fractures. The garnets are grossular-andradite type, with higher values for HREE over LREE, and low values for Rb, Sr, Ba, Pb and U. The skarn formation is related with the intrusion of the magma which causes the heating of the metamorphic rocks (rich in carbonate material – chlorite-sericite-carbonite, sericite-carbonate schists, etc.) from the low-grade metamorphic rocks. The Fe+3–Al+3 exchanges in the cores of the garnets indicate their formation from fluids with high oxygen fugacity.

Magmatic-hydrothermal evolution of the aquamarine-bearing Yamrang Pegmatite, Eastern Nepal: Insights from beryl, garnet, and tourmaline mineral chemistry

The Ikhabu Pegmatite Field (IPF) in the Nepal Himalaya is a newly discovered rare-element (REL) pegmatite field that hosts the Yamrang pegmatite, the primary source of the famous Nepalese aquamarines. In this contribution, we provide a comprehensive description of the geology of both the IPF and the Yamrang pegmatite, offering insights into the evolutionary stages of the Yamrang pegmatite based on its internal texture and the mineral chemistry of beryl, garnet, and tourmaline. The Yamrang pegmatite is classified as a beryl-columbite subtype of REL pegmatite, exhibiting axial symmetric zonation and is differentiated into five mineralogical-textural zones during magmatic and hydrothermal stages. The magmatic stage involves undercooling, disequilibrium crystallization, and fractional crystallization whereas the hydrothermal stage comprises alkali-enriched fluid exsolution, the formation of miarolitic cavities, and the crystallization of aquamarine. Yamrang aquamarines are enriched in FeO, up to 1.1 wt%, with Fe2+ as the primary chromophore, resulting in their blue color. Two types of beryl have been identified: magmatic beryl in zones 3 and 4 and hydrothermal beryl in miarolitic cavities (zone 5). Magmatic beryls are characterized by their alkali-poor to sodic composition, prismatic to columnar habit, homogeneous texture, and the presence of Fe-Al octahedral substitution. In contrast, hydrothermal beryls belong to the sodic to Li-Cs beryl group, with tabular to acicular habit, weak compositional zoning, and channel-tetrahedral substitution. Yamrang garnet belongs to the almandine-spessartine series, while the tourmalines are Mg-Ca rich dravite-schorl to Fe-Mn rich schorl variety. Alkali-poor to Li-Cs beryl with low REE contents, spessartine garnet (spessartine component, Xsps ∼ 52) with high HREE, and schorl with high Ti but low Li, Pb, and REE contents suggests that the Yamrang Pegmatite is an intermediate-fractionated REL pegmatite. Potential pegmatite evolution indicators for IPF include high alkali, Fe, Mn, and Rb contents in beryl, high Xsps in garnet, and an increase in Li, Fe, Mn, Zn, Ga, and Nb, alongside depletion of Mg, Ca, Ti, and Ta in schorl. The identification of a rare metal pegmatite field in the Nepalese Himalaya reinforces the general rare metal mineralization potential of the entire Himalaya region.

Provenance changes revealed by a multi-proxy approach to sandstone analysis and its implications on palaeogeography: Mesozoic Kutch Basin, India

Sedimentary rocks preserve the geological history of a basin and play a key role in constraining the palaeogeography. The Mesozoic Kutch Basin (India) comprises a number of sub-basins representing a pericratonic rift formed during the break-up of Gondwanaland. It preserves sediment deposited during the rifting and drifting of the Indian subcontinent. The current study identifies evidence of provenance changes recorded in Mesozoic sandstone units using a multi-proxy approach of quantitative modal analysis, quantitative heavy-mineral analysis and garnet chemistry. The Mesozoic sedimentary successions in the sub-basins are classified as the Kutch Mainland Group (KMG), the Pachchham Island Group (PIG) and the Eastern Kutch Group (EKG). Although the sub-basins are thought to share sediment from common source areas and the sandstone units are highly mature quartz arenites, the heavy-mineral assemblages (especially the content of zircon, tourmaline, rutile, apatite and staurolite) indicate previously unreported variation in the sediment source for the PIG when compared to the KMG and EKG. Moreover, an increase in the content of staurolite and kyanite in combination with rising trends of the ratios of staurolite–kyanite and zircon–tourmaline–rutile over garnet (St + Ky/Grt and ZTR/Grt) for the Callovian and younger strata is observed in the KMG and EKG. The above indicates a change in source from the older to the younger strata in each of the two sub-basins. The absence of their coeval strata in the PIG gives credence to the previously postulated rise of a subsurface basement high, the Median High in this basin. However, the timing of the rise remained so far unspecified, mentioned as “later in Jurassic” (Biswas, 2016b). The observations made in the current study constrain the rise of the Median High in the Kutch Basin to the Callovian time. The similarities in trends of the ratio of heavy minerals and garnet chemistry as well as variations in igneous garnet suggest recycling within the Kutch Basin from the Callovian to Oxfordian–Kimmeridgian strata in the EKG to the Kimmeridgian to Albian strata in the KMG.Besides revealing previously unknown details in the evolutionary and palaeogeographic history of the different sub-basins constituting the Kutch Basin, this multi-proxy study demonstrates the high potential of using recently developed techniques in provenance analysis i.e., the semi-automated heavy-mineral analysis by Raman spectroscopy and the state-of-the-art machine-learning aided garnet discrimination scheme. This study also provides a globally applicable workflow for other sedimentary basins, especially rift basins characterised by overall highly mature quartz arenites.

Post-magmatic processes recorded in bimodal chromitites of the East Chalkidiki meta-ultramafic bodies, Gomati and Nea Roda, Northern Greece

The meta-ultramafic bodies of Gomati and Nea Roda are situated in the Serbomacedonian Massif. They demonstrate bimodal character in terms of chromitite chemistry with both Cr- and Al-rich chromitites outcropping in proximity, with no obvious tectonic structure intercepting those two varieties. Based on the trace element abundances in spinel grains, metamorphosis reached amphibolite facies, forming porous spinel. Chromitite-hosted chlorite and garnet chemistry correlates with greenschist facies temperatures and formation of zoned spinel grains. Despite the metamorphic overprint, some of the primary features of the chromitites have been preserved. The PGE contents demonstrate an increase in Pd/Ir ratios in some chromitites pointing to fractionation, whereas low ratios of mostly Cr-rich chromitites point to partial melting being the main mechanism that controls PGE mineralization. The normalized trace element patterns of spinel-group minerals revealed that Al-rich chromitites were generated in spreading settings in a back-arc and the Cr-rich counterparts in SSZ environment. The parental melts of Al-rich and Cr-rich chromitites demonstrate MORB and boninitic affinities, respectively. The meta-ultramafic protoliths were modified within a subduction zone, with significant input of a sedimentary source, as confirmed by the chemistry of serpentinite, diopside and Sb-mineralization. These results suggest common geotectonic processes within the Rhodope and the Serbomacedonian massif, that have affected the ultramafic bodies and chromitite occurrences.

The retrograde evolution of F-rich skarns: Clues from major and trace element chemistry of garnet, scheelite, and vesuvianite from the Belka Pahar wollastonite deposit, India

Skarn settings host many ore deposits and are ideal for studying the mobility of elements in hydrothermal fluids. Belka Pahar, in the Sirohi district of Rajasthan (NW India), is the largest wollastonite deposit in India (estimated wollastonite reserve of 56 million tonnes). No detailed textural and geochemical study has been conducted on these skarn rocks. In this study, we use petrographic studies, and major-trace element chemistry of skarn minerals from Belka Pahar to deduce the sequence of mineral transformations and to characterize the changes in the composition of the fluid with the progress of fluid-rock interaction during skarn formation. Two major rock types from the exoskarn have been considered for detailed study: prograde skarn rocks comprising pyroxene, garnet, wollastonite, quartz, and calcite, and retrograde skarn rocks containing garnet, scheelite, vesuvianite, fluorite, and sphalerite. Two types of garnet are recognized in the rocks-texturally earlier prograde garnet (Grt 1 ) and texturally late retrograde oscillatory-zoned Grt 2 , which is further sub-divided into three generations Grt 2a , Grt 2b and Grt 2c . The Grt 1 (And 27–47 ) and Grt 2a (And 50–60 ) have high Y-concentrations, and high HREE/LREE ratio, which is in stark contrast to the late Grt 2b (And 40–50 ) and Grt 2c (And 27–40 ), which is characterized by high F, low Y-concentrations, and HREE-depleted REE patterns. The chemistry of different generations of garnet suggests a shift from diffusive to more advective metasomatic conditions and increasing water/rock ratio, accompanied by a shift in pH of the fluid from neutral to acidic to weakly acidic. The crystallization of F-rich garnet, vesuvianite, and fluorite indicates an increase in F-concentration in the later-stage fluid. An increase of W concentration in Grt 2b and co-precipitation of scheelite and fluorite also suggests its possible link with scheelite crystallization. The high grossular component of Grt 2b and Grt 2c suggests transport of Al in the hydrothermal fluid as F-complexes. The hydrothermal fluid composition extrapolated from scheelite chemistry agrees with the LREE enriched patterns exhibited by all skarn minerals. Principal Component Analysis done on a compiled dataset of skarn garnet shows that its trace element composition can be a useful proxy of fluid composition and can be used as an indicator of associated ore type. • Garnet composition is a useful proxy of fluid chemistry in the skarn system. • High F concentration in fluid enhanced Al mobilization, forming grossular-rich garnet. • Scheelite precipitation is linked to interaction of F-rich fluid with calc-silicate rocks. • PCA shows control of fluid composition on garnet chemistry. • Garnet trace element chemistry is a robust proxy of ore-genetic association.

Crystal chemistry of rare-earth containing garnets: Prospects for high configurational entropy

Materials with high degrees of lattice configurational entropy are being studied to assess their potential as highly-stable materials with potentially new and unusual properties. This report involves an assessment of the prospects for producing novel, complex multi-component oxide compounds that have the garnet crystal structure. We examine the crystal chemistry of garnets in an effort to determine if it may be possible to design so-called “high-entropy oxide” garnets, i.e., garnets containing numerous cation components, such that the compounds are stable, monophasic, and offer the potential for new and unusual physical properties. In this report, we quantify configurational entropy for compounds such as garnet that possess numerous cation sublattices. Then, we consider coordination polyhedra and details of bonding in rare-earth containing garnets, in an effort to predict structural aspects of multi-component oxide garnets.

Magmatic and post-magmatic evolution of post-collisional rare-metal bearing granite: The Neoproterozoic Homrit Akarem Granitic Intrusion, south Eastern Desert of Egypt, Arabian-Nubian Shield

The Homrit Akarem granitic intrusion (HAGI) outcrops near the western edge of the south Eastern Desert basement exposure in Egypt. It is a composite of two cogenetic intrusive bodies: an early albite granite phase shallowly emplaced at the apex of a magmatic cupola, and a later subjacent pink granite phase with a marginal zone of muscovite granite and better preservation of magmatic features. Mineral chemistry of primary biotite and garnet, together with whole-rock chemistry, identify the HAGI as a highly fractionated A-type peraluminous intrusion. The chemistry of F-dominant, Li-bearing, Fe3+-rich primary magmatic mica in the pink granite resembles that typically found in highly evolved Nb-Y-F pegmatites. The HAGI is the evolved product of a primary magma generated by partial melting of juvenile crust of the Arabian-Nubian Shield (ANS), emplaced along a regional strike-slip fault system that promoted its ascent. The main emplacement mechanism and evolutionary sequence of the HAGI was magmatic, although secondary minerals and textures resulting from hydrothermal fluid interactions are observed, especially at its margins. Primary columbite-(Mn) crystallized from melt and was partly replaced by secondary fluorcalciomicrolite. The high fluorine content of magmatic fluids exsolved from the intrusion is indicated by quartz-fluorite veins, greisenization, albitization, and F-bearing secondary oxide minerals. The magmatic derivation of this fluid is demonstrated by the F-dominant primary mica, a siderophyllite-polylithionite solid solution commonly known as zinnwaldite. The chemistry of zinnwaldite constrains the F/OH activity ratio and oxygen fugacity of its parental melt and thereby resolves the ambiguity between pressure and the effects of F in controlling the normative quartz content of rare-metal granites. The HAGI is less mineralized than the post-collisional rare-metal granites found further east in the south Eastern Desert, replicating a trend observed previously in the central Eastern Desert and suggesting that east-west zoning in rare metal enrichment is a persistent feature across latitudes at the western edge of the ANS.

In-situ U–Pb geochronology of Ti-bearing andradite as a practical tool for linking skarn alteration and Pb–Zn mineralization: A case study of the Mengya’a deposit, tibet

Ti-bearing andradite (Ti-Grt) occurs in a variety of geological environments, such as Si-unsaturated igneous rocks, high-temperature metamorphic rocks, and contact-metasomatized skarns. This type of garnet remains stable throughout a wide range of pressure-temperature conditions. Abundant skarn Pb–Zn deposits, where the ore-related pluton is not exposed, have been discovered along the eastern Nyainqentanglha metallogenic belt, western China. However, the mineralization age of these skarn Pb–Zn deposits remains controversial. Therefore, in this study, petrography, geochemistry, and in-situ U–Pb geochronology of the Ti-Grt are investigated together with the Re–Os geochronology of the molybdenite in the large Mengya’a Pb–Zn deposit. The potential of Ti-Grt dating is explored and the age relationships between the skarn alteration and the Pb–Zn mineralization are constrained. The results show Ti-Grt samples from the Mengya’a deposit are brown-black in color with TiO2-rich (mean of 3.47 wt%) features. Laser ablation inductively coupled plasma mass spectrometry dating showed that these Ti-Grts have a U–Pb age range of 54.9–53.8 Ma, which is consistent with the ages of two adjacent molybdenite Re–Os models (53.36–52.86 Ma). This indicates that the skarn alteration is temporally associated with a Pb–Zn mineralization event during the Indian-Asian main-collisional orogeny. The positive linear Ti vs. U correlation of the Ti-Grts and other compiled data indicate that Ti-bearing garnets may have high contents of U. The incorporation of U and Ti in garnet is largely controlled by the crystal chemistry of garnet and the components of hydrothermal fluids in a nearly closed system. Thus, this study confirms the reliability and accuracy of in-situ U–Pb dating of Ti-Grt and emphasizes that Ti-bearing garnets can become an invaluable geochronological tool for magmatic, metamorphic, and hydrothermal mineral assemblages.

The peridotite deformation cycle in cratons and the deep impact of subduction

Xenoliths play a crucial role in interpretation of mantle deformation and geochemistry. The classic work of Mercier and Nicolas (1975) introduced the concept of the peridotite deformation cycle, which connected observed microstructures to a physical sequence of deformation. We revisit Mercier and Nicolas' original concept, bringing in new constraints using large area EBSD maps and associated microstructural datasets, analysis of water contents in nominally anhydrous minerals, and trace element chemistry of pyroxenes and garnets. We apply these techniques to a well-characterized suite of peridotite xenoliths from the Eocene-age Homestead and Williams kimberlites in the northwestern Wyoming Craton. Pyroxene water content and trace element mineral chemistries reveal ubiquitous hydrous metasomatism beneath the craton, most likely linked to the Cenozoic Laramide Orogeny. Homestead xenoliths primarily exhibit coarse protogranular and equigranular textures, B-type olivine fabrics, and generally elevated mineral water contents compared to Williams. Xenoliths from Williams are strongly deformed, with porphyroclastic and transitional textures containing annealed olivine tablets, mostly A-type olivine fabrics, and generally lower mineral water contents. As a whole, mantle from Homestead to Williams reflects a cratonic scale deformation cycle that likely initiated in Laramide times and lasted until the end of orogeny in the Eocene. At Williams, evidence for a rapid deformation “sub-cycle” within the main deformation cycle is preserved in the tablet-bearing xenoliths, corresponding to the enigmatic “transitional” texture of Mercier and Nicolas (1975). Our results suggest that this texture reflects interruption of the main deformation cycle by processes possibly related to a rapidly forming lithospheric instability and generation of the kimberlite magma – offering a new interpretation of this ambiguous peridotite texture. Collectively, our results incorporate typically disparate geochemical and textural datasets on xenoliths to shed new insights into how metasomatism, volatiles, and deformation are connected in the deep cratonic lithosphere.

Typomorphic properties of kimberlite indicator minerals and their use in forecasting diamond deposits on the Siberian Platform

The results of mantle nodule investigations in kimberlite diatremes of the main Siberian Platform diamondiferous regions were analyzed. Morphology and chemistry of garnets, chrome-diopsides, clinopyroxenes, olivines, picro-ilmenites, chromites, chrome-spinellids and diamonds were investigated in detail. Generally, the quantity of diamond association minerals is proportional to diamond potential of a certain kimberlite variety for each type of kimberlite rocks composing pipes.

Spatial Distribution and Provenance of Detrital Minerals of Surface Sediment in the Okhotsk Sea

The Okhotsk Sea is a distinctive marginal sea in the northwestern Pacific Ocean, which is characterized by the prevalence of seasonal sea ice in winter. Sediment is sourced from the around region through sea ice transportation, rivers input, and volcanic eruptions. Surface sediments of the Okhotsk Sea shelf vary greatly in grain size, and the sand content is generally high, which is conducive to source-to-sink studies using ice-rafted detritus (IRD),detrital minerals and single mineral geochemistry methods. In this paper, the 63–125 μm grain size fraction was selected for the detrital minerals analysis of surface sediments (top 0–10 cm) from 58 sediment stations and 15 stations samples has been chosen for garnet chemistry. These stations are mainly located in the south central Okhotsk Sea. The distribution and composition of the heavy minerals are influenced by material derived from the Amur River, the north shelf (Okhotsk-Chukotka volcanic belt), Sakhalin Island, the Kamchatka Peninsula, and the Kuril Islands. The detrital mineral results show that hornblende, epidote and garnet are terrigenous material indicators. High contents of fresh hypersthene can be used as an indicator of volcanic eruption materials. And high content of abraded hypersthene can be used as an indicator of Okhotsk-Chukotka volcanic materials. In the northern Okhotsk Sea, the southward moving sea ice produced in Sakhalin Bay collides with the sea ice produced off the east coast of Sakhalin Island, which causes the sea ice to accumulate to the southeast. This results in the deposited ice-rafted debris having a southeastward facing fan shape, and the geochemical analysis of the garnet supports this conclusion. From west to east, the amount of material from Sakhalin Island gradually decreases, while the amount of material from the Amur River and Chukchi-Kamchatka increases.

Magmatic Evolution of Garnet-Bearing Highly Fractionated Granitic Rocks from Macao, Southeast China: Implications for Granite-Related Mineralization Processes

The widespread W-(Mo)-Sn-Nb-Ta polymetallic mineralization in Southeast (SE) China is genetically associated with Mesozoic highly fractionated granitic rocks. Such rocks have enigmatic mineralogical and geochemical features, making its petrogenesis an intensely debated topic. To better understand the underlying magma evolution processes, petrography, garnet chemistry and whole-rock major and trace element data are reported for Jurassic highly fractionated granitic rocks and associated microgranite and aplitepegmatite dikes from Macao and compared with coeval similar granitic rocks from nearby areas in SE China. Despite the fact that the most evolved rocks in Macao are garnet-bearing aplite-pegmatite dikes, the existence of coeval two-mica and garnet-bearing biotite and muscovite granites displaying more evolved compositions (e.g, lower Zr/Hf ratios) indicates that the differentiation sequence reached higher degrees of fractionation at a regional scale. Although crystal fractionation played an important role, late-stage fluid/melt interactions, involving F-rich fluids, imparted specific geochemical characteristics to Macao and SE China highly fractionated granitic rocks such as the non-CHARAC (CHArge-and-RAdius-Controlled) behavior of trace elements, leading, for example, to non-chondritic Zr/Hf ratios, Rare Earth Elements (REE) tetrad effects and Nb-Ta enrichment and fractionation. Such process contributed to the late-stage crystallization of accessory phases only found in these highly evolved facies. Among the latter, two populations of garnet were identified in MGI (Macao Group I) highly fractionated granitic rocks: small grossular-poor euhedral grains and large grossular-rich skeletal garnet grains with quartz inclusions. The first group was mainly formed through precipitation from highly evolved Mn-rich slightly peraluminous melts under low-pressure and relatively low temperature (∼700 °C) conditions. Assimilation of upper crust metasedimentary materials may have contributed as a source of Mn and Al to the formation of garnet. The second group has a metasomatic origin related to the interaction of magmatic fluids with previously crystallized mineral phases and, possibly, with assimilated metasedimentary enclaves or surrounding metasedimentary strata. The highly fractionated granitic rocks in Macao represent the first stage in the development of granite-related W-(Mo)-Sn-Nb-Ta mineralization associated with coeval more evolved lithotypes in SE China.

Evaluating the Formation Pressure of Diamond‐Hosted Majoritic Garnets: A Machine Learning Majorite Barometer

AbstractDiamond‐hosted majoritic garnet inclusions provide unique insights into the Earth's deep, and otherwise inaccessible, mantle. Compared with other types of mineral inclusions found in sub‐lithospheric diamonds, majoritic garnets can provide the most accurate estimates of diamond formation pressures because laboratory experiments have shown that garnet chemistry varies strongly as a function of pressure. However, evaluation using a compilation of experimental data demonstrates that none of the available empirical barometers are reliable for predicting the formation pressure of many experimental majoritic garnets and cannot be applied with confidence to diamond‐hosted garnet inclusions. On the basis of the full experimental data set, we develop a novel type of majorite barometer using machine learning algorithms. Cross validation demonstrates that Random Forest Regression allows accurate prediction of the formation pressure across the full range of experimental majoritic garnet compositions found in the literature. Applying this new barometer to the global database of diamond‐hosted inclusions reveals that their formation occurs in specific pressure modes. However, exsolved clinopyroxene components that are often observed within garnet inclusions are not included in this analysis. Reconstruction of inclusions, in the 8 cases where this is currently possible, reveals that ignoring small exsolved components can lead to underestimating inclusion pressures by up to 7 GPa (∼210 km). The predicted formation pressures of majoritic garnet inclusions are consistent with crystallization of carbon‐rich slab‐derived melts in Earth's deep upper mantle and transition zone.

Life-cycle analysis of coesite-bearing garnet

AbstractDetrital coesite-bearing garnet is the final product of a complex geological cycle including coesite entrapment at ultra-high-pressure conditions, exhumation to Earth’s surface, erosion and sedimentary transport. In contrast to the usual enrichment of high-grade metamorphic garnet in medium- to coarse-sand fractions, coesite-bearing grains are often enriched in the very-fine-sand fraction. To understand this imbalance, we analyse the role of source-rock lithology, inclusion size, inclusion frequency and fluid infiltration on the grain-size heterogeneity of coesite-bearing garnet based on a dataset of 2100 inclusion-bearing grains, of which 93 contain coesite, from the Saxonian Erzgebirge, Germany. By combining inclusion assemblages and garnet chemistry, we show that (1) mafic garnet contains a low number of coesite inclusions per grain and is enriched in the coarse fraction, and (2) felsic garnet contains variable amounts of coesite inclusions per grain, whereby coesite-poor grains are enriched in the coarse fraction and coesite-rich grains extensively disintegrated into smaller fragments resulting in an enrichment in the fine fraction. Raman images reveal that: small coesite inclusions of dimension < 9 µm are primarily monomineralic, whereas larger inclusions partially transformed to quartz; and garnet fracturing, fluid infiltration and the coesite-to-quartz transformation is a late process during exhumation taking place at c. 330°C. A model for the disintegration of coesite-bearing garnet enables the heterogeneous grain-size distribution to be explained by inclusion frequency. High abundances of coesite inclusions cause a high degree of fracturing and fracture connections to smaller inclusions, allowing fluid infiltration and the transformation to quartz, which in turn further promotes garnet disintegration.

Fluid Composition and its Evolution in the Belka Pahar Wollastonite Skarn, India: Clues from Skarn Mineral Chemistry with Special Focus on Garnet Chemistry

Fluid Composition and its Evolution in the Belka Pahar Wollastonite Skarn, India: Clues from Skarn Mineral Chemistry with Special Focus on Garnet Chemistry

Mineral chemistry and genetic implications of garnet from the São João del Rei Pegmatitic Province, Minas Gerais, Brazil

The pegmatites of the São João del Rei Pegmatitic Province are related to the Siderian protoliths of the Cassiterita and Resende Costa orthogneisses and to the Ritápolis metagranitoid of Ryacian age. Chemical analysis of garnet from twelve pegmatites reveal two different types of grains, which were found in the same pegmatitic body in six of these samples. One garnet type has almandine-spessartine composition (Sps11-7-58.8 Alm36.8-86.5 Prp0.1-4.1Grs0.0-1.4Adr0.0-2.6), grains with orange and pink tones, and scarce mineral inclusions. These garnet grains may have been formed at the magmatic stage of pegmatite crystallization. The composition of these grains plot exclusively on the Alm-Sps axis at the Prp+Grs+Adr+Uvr × Alm × Sps diagram, as expected from garnet crystallized in pegmatites, and an expansion of the field associated to pegmatites is proposed. The second type has a distinct chemical composition (Sps26.9-84.8Alm3.6-40.0 Prp0.0-10.4 Grs9.3-45.6 Adr0.1-3.4), displaying enrichment in Ca. This Ca-enriched garnet has irregular shaped colourless grains and abundant mineral inclusions. These grains may have been formed by Ca-metasomatism during the late-stage crystallization of the pegmatites.