Search Results (36)

The Junggar Basin contains a large amount of coal resources and is an important coal production base in China. The coal seam in Zhundong coalfield has a large single-layer thickness and high content of inertinite, but large particle Fe-sulphide minerals are associated with coal seams in some mining areas. A series of economic and environmental problems caused by the combustion of large-grained Fe-sulphide minerals in coal have seriously affected the economic, clean and efficient utilization of coal. In this paper, the ultra-thick coal seam of the Xishanyao formation in the Yihua open-pit mine of the Zhundong coalfield is taken as the research object. Through the analysis of coal quality, X-ray fluorescence spectrometer test of major elements in coal, inductively coupled plasma mass spectrometry test of trace elements, SEM-Raman identification of Fe-sulphide minerals in coal and LA-MC-ICP-MS test of sulfur isotope of marcasite, the coal quality characteristics, main and trace element characteristics, macro and micro occurrence characteristics of Fe-sulphide minerals and sulfur isotope characteristics of marcasite in the ultra-thick coal seam of the Xishanyao formation are tested. On this basis, the occurrence state and genesis of large particle Fe-sulphide minerals in the ultra-thick coal seam of the Xishanyao formation are clarified. The main results and understandings are as follows: (1) the occurrence state of Fe-sulphide minerals in extremely thick coal seams is clarified. The Fe-sulphide minerals in the extremely thick coal seam are mainly marcasite, and concentrated in the YH-2, YH-3, YH-8, YH-9, YH-14, YH-15 and YH-16 horizons. Macroscopically, Fe-sulphide minerals mainly occur in three forms: thin film Fe-sulphide minerals, nodular Fe-sulphide minerals, and disseminated Fe-sulphide minerals. Microscopically, they mainly occur in four forms: flake, block, spearhead, and crack filling. (2) The difference in sulfur isotope of marcasite was discussed, and the formation period of marcasite was preliminarily divided. The overall variation range of the δ³⁴S value of marcasite is wide, and the extreme values are quite different. The polyflake marcasite was formed in the early stage of diagenesis and the δ³⁴S value was negative, while the fissure filling marcasite was formed in the late stage of diagenesis and the δ³⁴S value was positive. (3) The coal quality characteristics of the thick coal seam were analyzed. The organic components in the thick coal seam are mainly inertinite, and the inorganic components are mainly clay minerals and marcasite. (4) The difference between the element content in the thick coal seam of the Zhundong coalfield and the average element content of Chinese coal was compared. The major element oxides in the thick coal seam are mainly CaO and MgO, followed by SiO₂, Al₂O₃, Fe₂O₃ and Na₂O. Li, Ga, Ba, U and Th are enriched in trace elements. (5) The coal-accumulating environment characteristics of the extremely thick coal seam are revealed. The whole thick coal seam is formed in an acidic oxidation environment, and the horizon with Fe-sulphide minerals is in an acidic reduction environment. The acidic reduction environment is conducive to the formation of marcasite and is not conducive to the formation of pyrite. (6) There are many matrix vitrinite, inertinite content, clay content, and terrigenous debris in the extremely thick coal seam. The good supply of peat swamp, suitable reduction environment and pH value, as well as groundwater leaching and infiltration, together cause the occurrence of large-grained Fe-sulphide minerals in the extremely thick coal seam of the Xishanyao formation in the Zhundong coalfield. Full article

A combination of microstructural, fluid inclusion, and in situ sulfur isotopic analyses of pyrite, along with major and trace element studies of the mineralization-hosting sandstone, reveals the complexity of its genesis from the Jurassic Toutunhe Formation in the Liuhuanggou sandstone-hosted uranium deposit, Southern Junggar Basin. Based on field geological investigations and the geochemical characteristics, it is concluded that the source of the ore-bearing sandstones originates from felsic igneous rocks in the Northern Tianshan and Central Tianshan regions. Through optical microscopy and scanning electron microscopy (SEM), three generations of pyrite were identified: framboidal pyrite, concentric overgrown pyrite, and sub-idiomorphic to idiomorphic cement pyrite. The sulfur isotopes of the pyrite were analyzed using laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). The results indicate that each type of pyrite has distinct sulfur isotope compositions (the framboidal pyrite: −16.85‰ to +2.16‰, the concentric overgrown pyrite: −7.86‰ to +10.32‰, the sub-idiomorphic to idiomorphic cement pyrite: +9.16‰ to +16.77‰). The framboidal pyrite and the sub-idiomorphic to idiomorphic cement pyrite were formed through bacterial sulfate reduction (BSR), while the concentric overgrown pyrite was formed through thermochemical sulfate reduction (TSR) triggered by the upward migration of hydrocarbons. The discovery of hydrocarbon inclusions provides evidence for the involvement of deep-seated reducing fluids in uranium mineralization. Uranium mineralization occurred in two distinct stages: (1) The early stage involved the interaction of uranium-bearing fluids with reductants in the mineralization-hosting strata under the influence of groundwater dynamics, leading to initial uranium enrichment. (2) The later stage involved the upward migration of deep-seated hydrocarbons along faults, which enhanced the reducing capacity of the sandstone and resulted in further uranium enrichment and mineralization. Full article

The Jiepailing deposit in southern Hunan is a typical large to super-large polymetallic tin deposit enriched in beryllium and other rare metals. To enhance the understanding of the mineralization processes of the Jiepailing deposit, detailed mineralogical, in situ geochemical, and sulfur isotopic analyses were conducted on pyrite closely associated with tin–polymetallic mineralization. Five types of pyrite have been identified in the deposit: (1) euhedral to subhedral medium- to coarse-grained pyrite (PyI) in tungsten–tin ore; anhedral fine-grained pyrite (PyII) in tin polymetallic–fluorite ore; anhedral fine-grained or aggregate pyrite (PyIII) in lead–zinc ore; euhedral to subhedral coarse-grained pyrite (PyIV) in beryllium–fluorite mineralization; and subhedral to anhedral fine-grained pyrite (PyV) in carbonate veinlets developed in the wall rock. Backscattered electron imaging indicates consistent structural features across the five types of pyrite. In situ trace element analysis reveals differences in trace element concentrations among the pyrite types. PyI is relatively enriched in Sn, Cu, and Co. In contrast, PyIII is enriched in Pb, Zn, Sn, and Ti, while PyIV and PyV are enriched in Ag and Sb. PyI has a Co/Ni ratio more than 1, while the Co/Ni ratios in the other four types of pyrite are less than 1. LA-MC-ICP-MS in situ sulfur isotope analysis shows δ³⁴S values ranging from 2.5‰ to 5.8‰ (average 4.3‰, PyI), 2.5‰ to 5.8‰ (average 4.3‰, PyII), −7.6‰ to 9.5‰ (average 3.9‰, PyIII), −3.7‰ to 10.6‰ (average 3.6‰, PyIV), and 6.8‰ to 14.1‰ (average 9.2‰, PyV). Based on previous studies, regional geological background, deposit characteristics, and the in situ trace element and sulfur isotope compositions of pyrite, it is inferred that the various ore bodies in the Jiepailing deposit are products of Late Cretaceous magmatic–hydrothermal activity. The early ore-forming fluid originated from magmatic sources and during the migration into the wall rock and shallow formations, mixed with fluids primarily derived from atmospheric precipitation. Temperature, pressure, and composition changed of the ore-forming fluid which carried a large amount of substances, leading to tungsten–tin, tin polymetallic–fluorite, lead–zinc, and beryllium–fluorite mineralization, followed by carbonation during the late-stage mineralization. Full article

Non-metallic inclusions (NMIs) in steel have a detrimental effect on the processing, mechanical properties, and corrosion resistance of the finished product. This is particularly evident in the case of macroscopic inclusions (>100 µm), which are rarely observed in steel castings produced using state-of-the-art technologies, whereby casting parameters are optimized towards steel cleanliness, and post-treatment steps such as vacuum arc remelting (VAR) are used, but frequently result in the rejection of the affected product. To improve production processes and develop effective countermeasures, it is essential to gain a deeper understanding of the origin and formation of NMIs. In this study, the potential of elemental and isotopic fingerprinting to trace the sources of macroscopic oxide NMIs found in VAR-treated steel ingots using SEM-EDX, inductively coupled plasma mass spectrometry (ICP-MS), laser ablation ICP-MS (LA-ICP-MS), and laser ablation multicollector ICP-MS (LA-MC-ICP-MS) were exploited. Following this approach, main and trace element content and ⁸⁷Sr/⁸⁶Sr isotope ratios were determined in two specimens of macroscopic NMIs, as well as in samples of potential source materials. The combination of the data allowed the drawing of conclusions about the processes leading to the formation of these inclusions. For both specimens, very similar results were obtained, indicating a common mechanism of formation. The inclusions were likely exogenous in origin and were primarily composed of calcium–aluminum oxides. They appeared to have undergone chemical modification during the casting and remelting process. The results indicate that particles from the refractory lining of the casting system most likely formed the macroscopic inclusions, possibly in conjunction with a second, calcium-rich material. Full article

The Xiong’ershan district is situated on the southern margin of the North China Craton (NCC) and located within the Qinling–Dabieshan Orogen’s orogenic zone. It is adjacent to the XiaoQinling mining district and exhibits very favorable geological conditions for mineralization, as the district contains numerous gold deposits, positioning it as one of the key gold-producing areas of China. The Miaoling gold deposit is a hydrothermal deposit and is controlled by the Mesozoic nearly NS-trending fault. The ore bodies are hosted in the Mesoproterozoic Xiong’er Group of the Changcheng System of volcanic rocks, with reserves reaching large-scale levels. Pyrite is the main gold-bearing mineral and can be classified into four generations: early-stage fine- to medium-grained euhedral to subhedral cubic pyrite (Py1); medium- to coarse-grained euhedral to subhedral cubic granular pyrite in quartz veins (Py2a); fine-grained subhedral to anhedral disseminated pyrite in altered rocks (Py2b); and late-stage anhedral granular and fine-veinlet pyrite in later quartz veins (Py3). Through in situ trace element analysis of the pyrite using LA-ICP-MS, a positive correlation between Au and As was observed during the main mineralization stage; gold mainly exists as a solid solution within the pyrite lattice, and the ablation signal curve reflecting the intensity of trace element signals showed that gold also occurs as micron-scale mineral inclusions. The trace element content suggested a gradual increase in oxygen fugacity from Stage 1 to Stage 2, followed by a decrease from Stage 2 to Stage 3. The Co/Ni values in the pyrite (0.56 to 62.02, with an average of 12.34) exhibited characteristics of magmatic hydrothermal pyrite. The in situ sulfur isotope analysis of the pyrite using LA-MC-ICP-MS showed δ³⁴S values of 4.24‰ for Stage 1, −6.63‰ to −13.79‰ for Stage 2, and −4.31‰ to −5.15‰ for Stage 3. Considering sulfur isotope fractionation, the δ³⁴S value of the hydrothermal fluid during the main mineralization stage was calculated to be between 0.31‰ and 2.68‰. Full article

As a potential strategic mineral resource, lithium (Li) in coal measures (including coal and parting) has attracted increasing attention from scholars globally. For a long time, Li in coal measures has been studied mainly on the macro-scale (whole rock); however, the microscopic characteristics of Li and Li isotope variations in coal measures are less well known. In this study, the No. 6 coal measures in the Haerwusu Mine were studied using ICP-MS, XRD, SEM-EDS, MC-ICP-MS, and LA-ICP-MS. The geochemical and mineralogical characteristics, the microscale distribution of Li in minerals, and the Li isotopes of Li-rich coal and parting in the No. 6 coal measure were investigated. The results show that the Li content in the No. 6 coal seam ranges from 3.8 to 190 μg/g (average 83 μg/g), which is lower than the parting (290 μg/g) and higher than the comprehensive evaluation index of Li in Chinese coal (80 μg/g). LA-ICP-MS imaging showed that Li in the coal is mainly contained within cryptocrystalline or amorphous lamellae aluminosilicate materials, and the Li content in lenticular aggregate kaolinite is low. The Li in parting is mainly found in illite/chlorite. The δ⁷Li of the coals was 3.86‰, which may be influenced by the input of the source rock. The δ⁷Li of the parting (7.86‰), which was higher than that of the coal, in addition to being inherited from the source rock, was also attributed to the preferential adsorption of ⁷Li by the secondary clay minerals entrapped in the parting from water during diagenetic compaction. Finally, by integrating the peat bog sediment source composition, sedimentary environment evolution, and Li isotope fractionation mechanism of No. 6 coal, a Li metallogenic model in the Li-rich coal measure was initially established. In theory, the research results should enrich the overall understanding of the Li mineralization mechanism in coal measures from the micro-scale in situ and provide a scientific basis for the comprehensive utilization of coal measure resources. Full article

The South China Plate is an important part of the Rodinia supercontinent in the Neoproterozoic. The Rizhao area, located on the northeastern margin of the South China Plate, records multiple periods of magmatism, among which Neoproterozoic granitic gneiss is of great significance to the tectonic evolution of the South China Block. In this study, systematic petrology, geochemistry, isotopic chronology, and zircon Hf isotopic analyses were carried out on gneisses samples of biotite alkali feldspar granitic and biotite monzogranitic compositions in the Rizhao area. Geochemical analyses suggest that these granitic rocks belong to the sub-alkaline series and have high potassium contents. They are enriched in large-ion lithophile elements K, Rb, and Ba; depleted in high field strength elements P, Nb, and Ti; enriched in light rare earth elements and moderately depleted in heavy rare earth elements; and have weak to moderate negative Eu anomalies and weak negative Ce anomalies. These rocks are post-orogenic A-type granites. LA-MC-ICP-MS U-Pb dating of zircons from two biotite alkali-feldspar granitic gneiss samples yielded weighted mean ages of 785 ± 8 Ma (MSWD = 3.0) and 784 ± 6Ma (MSWD = 1.5), respectively, and a biotite monzogranitic gneiss sample yielded a weighted mean age of 789 ± 6 Ma (MSWD = 2.3). Lu-Hf isotopic analyses on zircon grains from the two types of Neoproterozoic-aged gneisses yielded negative ε_Hf(t) values ranging from −19.3 to −8.8 and from −18.3 to −10.4, respectively, and the corresponding two-stage Hf model age ranges are 2848–3776 Ma and 2983–3682 Ma, respectively. These granites are the product of Neoproterozoic magmatic activity and are mainly derived from the partial melting of Archean continental crust. Combining the geochemical characteristics and zircon U-Pb-Lu-Hf isotopic analyses, these A-type granitic gneisses appear to have formed in an intracontinental rift extension environment during the initial break-up of the Rodinia supercontinent, as part of the supercontinent break-up process at the northeastern margin of the South China Block. Full article

Himalayan leucogranite is an excellent target for understanding the orogenic process of the India–Asia collision, but its origin and tectonic significance are still under debate. An integrated study of geochronology, geochemistry, and in situ Sr-Nd-Hf isotopes was conducted for a tourmaline-bearing leucogranite in the eastern Tethyan Himalaya using LA-ICP-MS, X-ray fluorescence spectroscopy, and ICP-MS and LA-MC-ICP-MS, respectively. LA-ICP-MS U-Pb dating of zircon and monazite showed that it was emplaced at ~19 Ma. The leucogranite had high SiO₂ and Al₂O₃ contents ranging from 73.16 to 73.99 wt.% and 15.05 to 15.24 wt.%, respectively. It was characterized by a high aluminum saturation index (1.14–1.19) and Rb/Sr ratio (3.58–6.35), which is characteristic of S-type granite. The leucogranite was enriched in light rare-earth elements (LREEs; e.g., La and Ce) and large ion lithophile elements (LILEs; e.g., Rb, K, and Pb) and depleted in heavy rare-earth elements (e.g., Tm, Yb, and Lu) and high field strength elements (HFSEs; e.g., Nb, Zr, and Ti). It was characterized by high I Sr (t) (0.7268–0.7281) and low ε Nd (t) (−14.6 to −13.2) and ε Hf (t) (−12.6 to −9.47), which was consistent with the isotopic characteristics of the Higher Himalayan Sequence. Petrogenetically, the origin of the leucogranite is best explained by the decompression-induced muscovite dehydration melting of an ancient metapelitic source within the Higher Himalayan Sequence during regional extension due to the movement of the South Tibetan Detachment System (STDS). The significantly high lithium and beryllium contents of the leucogranite and associated pegmatite suggest that Himalayan leucogranites possess huge potential for lithium and beryllium exploration. Full article

The Newark Basin comprises Late Triassic and Early Jurassic fluvio-lacustrine rocks (Stockton, Lockatong, Passaic, Feltville, Towaco, and Boonton Formations) and Early Jurassic diabase intrusions and basalt lava flows. Boron concentrations in private well water samples range up to 18,000 μg/L, exceeding the U.S. Environmental Protection Agency Health Advisory of 2000 μg/L for children and 5000 μg/L for adults. Boron was analyzed in minerals, rocks, and water samples using FUS-ICPMS, LA-ICP-MS, and MC ICP-MS, respectively. Boron concentrations reach up to 121 ppm in sandstone of the Passaic Formation, 42 ppm in black shale of the Lockatong Formation, 31.2 ppm in sandstone of the Stockton Formation, and 36 ppm in diabase. The δ¹¹B isotopic values of groundwater range from 16.7 to 32.7‰, which fall within those of the diabase intrusion (25 to 31‰). Geostatistical analysis using Principal Component Analysis (PCA) reveals that boron is associated with clay minerals in black shales and with Na-bearing minerals (possibly feldspar and evaporite minerals) in sandstones. The PCA also shows that boron is not associated with any major phases in diabase intrusion, and is likely remobilized from the surrounding rocks by the intrusion-related late hydrothermal fluids and subsequently incorporated into diabase. Calcite veins found within the Triassic rock formations exhibit relatively elevated concentrations ranging from 6.3 to 97.3 ppm and may contain micro-inclusions rich in boron. Based on the available data, it is suggested that the primary sources of boron contaminating groundwater in the area are clay minerals in black shales, Na-bearing minerals in sandstone, diabase intrusion-related hydrothermal fluids, and a contribution from calcite veins. Full article

Shallow-water carbonate rocks constitute a crucial component of large guyots, arising in distinct environments and harboring valuable insights into the evolutionary stages of seamount islands as well as the tectonic conditions of the underlying oceanic plate. Laser Ablation Multi-Collector Inductively Coupled Plasma Mass Spectrometry (LA-MC-ICP-MS) was used to conduct in situ U–Pb isotope dating of carbonate minerals with low uranium content collected from Weijia Guyot. This dating approach yielded crucial evidence for the vertical development of the seamount. Our study indicates that shallow-water carbonate rocks in Weijia Guyot had a temporal range between 91 My and 137 My. The carbonate rocks underwent two growth phases, Hauterivian to Barremian and Cenomanian to Turonian, with a hiatus of approximately 20 My. Since the Hauterivian age, the shield volcano of Weijia Guyot is essentially complete, with its seamount top exposed at or near sea level and receiving its first stage of shallow-water carbonate sedimentation. Based on the dating of both shallow-water carbonate rocks and hawaiite within the Weijia Guyot, it is inferred that approximately 10 My elapsed from shield-building volcanism to late alkalic volcanism. During the Turonian age, the main reason for the second phase of shallow-water carbonate rocks in the seamounts was the regional tectonic uplift triggered by the drift of the Weijia Guyot along with the Pacific Plate toward the Society hotspot. Full article

The gold deposit offshore of Northern Sanshandao is an ultra-large-scale gold deposit discovered in the Jiaodong ore area in recent years. This deposit is a fractured-zone altered-rock-type gold deposit; however, its ore genesis and precise mineralization processes are still highly controversial. Based on petrographical observation, the trace elements, sulfur isotopes, and rubidium–strontium isotopes of the gold-bearing pyrite were analyzed using LA-MC-ICP-MS to obtain the source of the ore-forming fluids and ore genesis. The results show that Au has a good positive correlation with Ag, As, and Cu. It is speculated that the As in the pyrite of the gold deposit offshore of Northern Sanshandao is in the form of As⁻, replacing S⁻ and entering the pyrite, causing its lattice defects, and thus promoting the entry of Au⁺ into the gold-bearing pyrite. The Co/Ni ratios mainly range between 0.1 and 10, indicating that the mineralization process has experienced different forms of hydrothermal evolution and the mixing of different fluids. The results of the in-situ sulfur isotope analysis show that pyrite δ³⁴S in the mineralization period is characterized by a high sulfur value. The authors of this study believe that the initial sulfur isotope composition has mantle-derived components. The large-scale, deep cutting, and high degree of fragmentation in the Sanshandao fault zone are conducive to the interaction between fluids and rocks, as well as the mixing and addition of seawater, resulting in the characteristic high δ³⁴S value. The Sr isotopic compositions indicate a crust–mantle mixing attribute of the mineralized material source. The Rb–Sr isochron age of the pyrite is 118.5 ± 0.65 Ma, which represents the age of gold mineralization. According to the characteristics of the trace elements and sulfur isotopes, it is inferred that the gold deposit minerals offshore of Northern Sanshandao originated from deep magmatic-hydrothermal reservoirs, and the mixing of seawater and Au–As-rich hydrothermal fluids was the formation mechanism of huge amounts of gold precipitation. Full article

The Jiaodong gold province is one of the most important gold fields globally and the largest in China. The Denggezhuang gold deposit is situated in the eastern portion of the Muping metallogenic belt, within the Jiaodong gold province. Despite many recent investigations, detailed mineralogical studies, particularly on auriferous minerals such as pyrite, are lacking. Therefore, further constraints on the occurrence mode and source of gold are necessary for this deposit. This study employed in situ laser ablation (multi-collector) inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) trace element and sulfur-lead isotopic analyses on pyrite at different stages. The aim was to reveal the occurrence status of various trace elements within Denggezhuang pyrite and to trace the complete evolution process of multi-stage fluids at Denggezhuang, elucidating the sources of gold mineralization. Four generations of pyrite in chronological order, Py-1, Py-2a, Py-2b, and Py-3, were identified via petrographic and backscattered electron (BSE) image analyses. Using in situ LA-MC-ICP-MS, we found that Co and Ni are most abundant in Py-1, while Py-2b is rich in As, Au, Ag, Pb, and Zn, reflecting the evolution of the mineralizing fluids in different mineralization stages. Py-2b contains a significant amount of invisible lattice gold, which migrates and precipitates within fluids rich in As. The in situ LA-MC-ICP-MS S-Pb isotopic analysis of pyrite indicates a relatively consistent source of ore-forming materials across different stages. Additionally, the S-Pb isotope characteristics resemble those of widely distributed coeval mafic dikes. Therefore, we propose that a water-rich, fertile, and deep-seated mafic magmatic system might have provided fluids, materials, and heat for mineralization. Full article

The use of analytical techniques is important and critical in all areas related to REE, such as basic fundamental research, exploration, mining, extraction, and metallurgical activities at different stages by different industries. At every stage of these activities, rock, ore, minerals, and other related materials have to be analyzed for their REE contents in terms of elemental, isotopic, and mineralogical concentrations using different analytical techniques. Spectacular developments have taken place in the area of analytical instrumentation during the last four decades, with some of them having shrunk in size and become handheld. Among laboratory-based techniques, F-AAS, GF-AAS, ICP-OES, and MP-AES have become very popular. Because of high sensitivity, fewer interference effects, and ease of use, ICP-MS techniques, such as quadrupole ICP-MS, ICP-MS/MS, ICP-TOF-MS, MH-ICP-MS, HR-ICP-MS, and MC-ICP-MS, with both solution nebulization as well as direct solid analysis using laser ablation sample introduction methods, have become more popular for REE analysis. For direct analysis of solids, INAA, XRF, and LIBS techniques, as well as LA-based ICP-MS techniques, are being extensively utilized. The LIBS technique in particular requires little to no sample preparation. TIMS, SIMS, and SHRIMP techniques are being used for isotopic as well as dating REE depots. Portable analytical techniques, such as pXRF, pLIBS, and Raman spectrometers are able to perform in situ analysis even in the field, helping to make fast decisions during exploration studies. At present, hyperspectral remote sensing techniques including handheld, drone, and satellite-based techniques have become very popular in REE exploration studies because of their ability to cover larger areas in a limited time and, thus, became very cost-effective. Deployment of microanalytical devices/sensors mounted in remotely operated vehicles (ROV) is being successfully utilized in detecting REE-rich deposits in the deep oceans. Providing updated in-depth information on all these important aspects with suitable examples, especially from the point of view of REE research studies is the focal point of this review article. Full article

In depth of the Simao Basin (2390 to 2650 m depth interval), many gray mudstone or carbonate rocks are developed in the red salt-related strata, and pyrite crystals are found in the fissure and matrix. In this study, petrology, mineralogy, element geochemistry, and LA-MC-ICP-MS in situ sulfur isotope analysis were used to constrain the genesis of pyrite, and the influence of relevant geological activities on potash mineralization was discussed. The results show that: (1) In the upper part of the salt layer, particle size of the pyrite ranges from 50 to 300 μm. The crystal morphology is mainly pentagonal-dodecahedral and irregularly granular, with a small amount of cuboidal pyrite. In the interlayer between rock salt, particle size of the pyrite is from 50 to 100 μm, and the crystals are mainly octahedral. (2) The S/Fe value of pentagonal-dodecahedral pyrite is significantly greater than 2; the S/Fe value of octahedral and cubic pyrite is less than 2; and the S/Fe value of irregular granular pyrite is close to 2. (3) The δ³⁴S_V-CDT values of pyrite in the upper salt-related strata range from −15.65‰ to 11.81‰, and the average δ³⁴S_V-CDT values of all samples range from 0.79‰ to 8.20‰. The δ³⁴S_V-CDT values of pyrite interlayer between rock salt range from −15.02‰ to −6.36‰, with an average value of −10.66‰. The above results indicate that the pyrite in the upper part of the rock salt layer was formed in a medium-low temperature hydrothermal environment, and the ore-forming sulfur elements have hydrothermal sources, bacterial sulfate reduction (BSR) sources, and thermochemical sulfate reduction (TSR) contributions. The pyrite between the rock salt layers is of sedimentary origin, and the ore-forming sulfur element comes from BSR. At present, there is no evidence of the influence of hydrothermal activities on deep potash-rich salt bodies, and the influence on the Mengyejing potash deposit has continued since the metallogenic period. Full article

In order to provide further insights into the origin of Ru-Os-Ir alloys, this study presents new highly siderophile element (HSE: Re, Os, Ir, Ru, Pt, and Pd) abundance and ¹⁸⁷Re-¹⁸⁷Os and ¹⁹⁰Pt-¹⁸⁶Os isotope data for detrital grains of native Ru-Os-Ir alloys in placer deposits of the Kunar and Unga Rivers, which display a close spatial association with the Kunar dunite–harzburgite complex in the northern part of the Taimyr Peninsula in the Polar Siberia. The study utilized electron microprobe analysis, negative thermal ionization mass-spectrometry (N-TIMS) and laser ablation multiple-collector inductively coupled plasma mass-spectrometry (LA MC-ICP-MS). The primary nature of the Ru-Os-Ir alloys is supported by the occurrence of euhedral inclusions of high-Mg olivine (Fo_92–93) that fall within the compositional range of mantle olivine. The LA MC-ICP-MS data show similar average initial ¹⁸⁷Os/¹⁸⁸Os and γ¹⁸⁷Os(740 Ma) values for PGM assemblages from the Kunar and Unga deposits of 0.1218 ± 0.0010, −0.18 ± 0.85, and 0.1222 ± 0.0025, +0.10 ± 2.1, respectively. These values are identical, within their respective uncertainties, to the initial ¹⁸⁷Os/¹⁸⁸Os value of the Ru-Os-Ir alloy grain measured by N-TIMS (0.1218463 ± 0.0000015, γ¹⁸⁷Os(740 Ma) = −0.1500 ± 0.0012). The combined ¹⁸⁷Re-¹⁸⁷Os isotopic data for all studied grains (γ¹⁸⁷Os(740 Ma) = −0.02 ± 1.6) indicate evolution of the Kunar and Unga mantle sources with a long-term chondritic ¹⁸⁷Re/¹⁸⁸Os ratio of 0.401 ± 0.030. In contrast to the ¹⁸⁷Os/¹⁸⁸Os data, the initial ¹⁸⁶Os/¹⁸⁸Os value of 0.1198409 ± 0.0000012 (µ¹⁸⁶Os(740 Ma) = +34 ± 10) obtained for the same Ru-Os-Ir alloy grain by N-TIMS is suprachondritic and implies evolution of the Kunar and Unga mantle source(s) with a long-term suprachondritic ¹⁹⁰Pt/¹⁸⁸Os ratio of 0.00247 ± 0.00021. This value is ~40% higher than the average chondritic ¹⁹⁰Pt/¹⁸⁸Os ratio of 0.00180 and indicates long-term enrichment of the Kunar source in Pt over Os. Establishing the source of this enrichment requires further investigation. Full article