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The Tower Hill gold deposit is distinguished from most Archaean lode deposits of the Yilgarn Craton by virtue of its formation early in the regional deformation history and its consequent deformation. The deposit is located in ultramafic schist, adjacent to the contact with a small pluton of biotite monzogranite that intrudes pervasively foliated granodiorite, the dominant component of the Raeside Batholith. Gold, accompanied by local concentrations of bismuth minerals and molybdenite, occurs in a number of quartz vein ‘packages‘. Mineralised quartz veins at Tower Hill lie within an envelope of potassic alteration (talc‐biotite‐chlorite‐pyrite schist), up to several hundred metres wide. They are spatially and temporally associated with the biotite monzogranite and felsic porphyry intrusions, and their deformed equivalents. The deposit lies in a broad zone of ductile deformation (the Sons of Gwalia Shear Zone). Within the altered ultramafic schist, thin units of felsic schist, derived from biotite monzogranite and felsic porphyry, provided sites of contrasting competency that localised quartz vein formation. The mineralised quartz veins were subsequently deformed during alternating periods of shortening and extension, probably related to the syntectonic, solid‐state emplacement of the Raeside Batholith. These deformations pre‐dated strike‐slip movement on the Cemetery Fault, which truncates the ductile fabrics of the Sons of Gwalia Shear Zone, south of Tower Hill. In terms of the regional deformation history, gold mineralisation at Tower Hill formed during early D2 (regional upright folding); subsequent deformation of the orebody pre‐dated D3 (strike‐slip movement on the Cemetery Fault). The nearby Sons of Gwalia and Harbour Lights deposits also probably formed at an early stage, in contrast to most lode gold deposits in the Yilgarn Craton, which formed during or after D3.  相似文献   

3.
The Shkol’noe deposit is localized in a small granitoid stock, the root portion of which is traced using geophysical data to a depth of 5–8 km. The high-grade gold ore (33 gpt Au) is enriched in silver and principally differs in ore composition from the previously studied mesothermal gold-quartz and epithermal gold-silver deposits in the Russian Northeast. The main reserves of the Shkol’noe deposit concentrate in bonanzas (20% of the total volume of orebodies). The internal deformation is related to the rearrangement of matter in freibergite; exsolution structures in fahlore and native gold are related to postmineral metamorphism. It is suggested that the ore of the Shkol’noe deposit occupies a transitional position between porphyrytype and epithermal levels of ore deposition.  相似文献   

4.
Stable isotope analyses of quartz, sulphides, and magnetite were conducted to provide information on thermal history and source of hydrothermal fluids in the Palaeoproterozoic Enåsen gold deposit. Reequilibration and homogenization of oxygen isotopes throughout the rock have apparently not occurred despite the upper amphibolite to granulite facies regional metamorphism that has affected the rocks. However, oxygen isotope geothermometry on a coexisting quartz-magnetite pair gave a minimum temperature for peak metamorphism of around 650 °C which agrees with Fe-Mg geothermometry. This suggests that grain-scale equilibrium is achieved. The variation in oxygen isotope ratios (18O = 7.3 – 10.5) on quartz from the metamorphosed acid sulphate alteration zone is suggested to represent a cooling trend in the fossil hydrothermal system with higher 18O-values in more superficial parts. Temperatures of alteration and silicification and isotopic composition of hydrothermal fluids could not be defined from the present data but it was recognized that the data is compatible with a epithermal genesis for the deposit. It is suggested that alteration, silicification, and mineralization at the Enåsen gold deposit took place in a high sulphidation epithermal environment at temperatures of around 200–250 °C and that the hydrothermal fluids consisted of meteoric and magmatic water. A tentative reconstruction of the fossil hydrothermal system is presented. Sulphur isotope ratios of sulphides from the fold-bearing quartz-sillimanite gneiss gave 34S-values close to zero indicating a magmatic source of the sulphur.  相似文献   

5.
The Tamlalt–Menhouhou gold deposit belongs to the Neoproterozoic–Palaeozoic Tamlalt inlier located in the Eastern High-Atlas (Morocco). It occurs in altered Upper Neoproterozoic bimodal volcanic and volcano-sedimentary units outcropping in the Tamlalt–Menhouhou area. Gold mineralization has been identified in quartz veins related to shear-zones associated with a strong quartz-phyllic-argillic alteration. Visible free gold is related to goethite–malachite–barite boxworks in quartz veins. The other alteration minerals accompanying gold mineralization are mainly carbonates, chlorite, hematite, albite and pyrite whose relative proportion defines three alteration types. 40Ar/39Ar geochronology performed on phengite grains from phyllic alteration and the auriferous quartz veins, yields plateau ages ranging from 300 ± 5 Ma to 284 ± 12 Ma with a weighted mean age of 293 ± 7 Ma. This identifies a Late Variscan age for the Tamlalt–Menhouhou “shear zones-related” gold deposit and emphasizes the consequences of the Variscan orogeny for gold mineralization in the High-Atlas and Anti-Atlas Neoproterozoic inliers.  相似文献   

6.
Generally, sandstone-type uranium deposits can be divided into three zones according to their redox conditions: oxidized zone, ore zone and reduced zone. The Dongsheng uranium deposit belongs to this type. In order to study its geochemical characteristics, 11 samples were taken from the three zones of the Dongsheng uranium deposit. Five samples of them were collected from the oxidized zone, four samples from the ore zone and two samples from the reduced zone. These samples were analyzed using organic and inorganic geochemical methods. The results of GC traces and ICP-MASS indicate that the three zones show different organic and inorganic geochemical characteristics.  相似文献   

7.
The Duolanasayi gold deposit, 60 km NW of Habahe County, Xinjiang Uygur Autonomous Region, is a mid-large-scale gold deposit controlled by brittle-ductile shearing, and superimposed by albitite veins and late-stage magma hydrothermal solutions. There are four types of pyrite, which are contained in the light metamorphosed rocks (limestone, siltstone), altered-mineralized rocks (chlorite-schist, altered albite-granite, mineralized phyllite), quartz veins and carbonatite veinlets. The pyrite is the most common ore mineral. The Au-barren pyrite is present mainly in a simple form and gold-bearing pyrite is present mainly in a composite form. From the top downwards, the pyrite varies in crystal form from {100} and {210} {100} to {210} {100} {111} to {100} {111}. Geochemical studies indicate that the molecular contents of pyrite range from Fe1.057S2 to Fe0.941S2. Gold positively correlates with Mn, Sr, Zn, Te, Pb, Ba and Ag. There are four groups of trace elements: Fe-Cu-Sr-Ag, Au-Te-Co, As-Pb-Zn and Mn-V-Ti-Ba-Ni-Cr in pyrite. The REE characteristics show that the total amount of REE (ΣREE) ranges from 32.35×10 -6 to 132.18×10 -6; LREE/HREE, 4.466-9.142; (La/Yb)N, 3.719-11.133; (Eu/Sm)N, 0.553-1.656; (Sm/Nd)N, 0.602-0.717; La/Yb, 6.26-18.75; δEu, 0.628-2.309; δCe, 0.308-0.816. Sulfur isotopic compositions (δ 34S=-2.46‰--7.02‰) suggest that the sulfur associated with gold mineralization was derived from the upper mantle or lower crust.  相似文献   

8.
The Dajing Cu-Sn-polymetallic ore deposit is famous for its large scale, abundant associated elements, narrow and closely-spaced development of ore veins and high grade, but exploration within the mining district and its deeper parts has revealed no Yanshanian rockbody. Therefore, there have been proposed a diversity of hypotheses on the genesis of the deposit. The authors, from the angle of mantle-branch structure, provided evidence showing that the mining district is located in the core of the Da Hinggan Ling mantle-branch structure, the multi-stage evolution of mantle plume paved the way for the ascending of deep-source ore fluids and these fluids extracted part of the ore-forming materials. Then, these ore-forming materials were concentrated in the favorable structural loci (e.g. structural fissures) to form ores. The orientation of ore-forming and ore-controlling fissures is closely related to the regionally structural stress field at the metallogenic stage. The zonation of Sn, Cu, Au, Ag, Pb, and Zn within the mining district appears to be related to metallogenesis and the crystallization temperature of ore-forming materials. Mineralization of Sn, Cu, Au, etc. which require relatively high crystallization temperature and pressure is in most cases recognized in the central part of the mining district, while that of Ag, Pb, Zn, etc. which require relatively low crystallization temperature and pressure is, for the most part, produced in the periphery of the mining district.  相似文献   

9.
The R?anovo deposit is a unique example of metamorphosed lateritic Fe-Ni deposits in the wellknown Vardar ophiolitic belt of the Balkans, where Fe-Ni mineralization is a product of the Early Cretaceous lateritic weathering mantle after Jurassic ultramafic rocks subsequently redeposited into the Cretaceous shallow-water marine basin. As a result, a layer of Fe-Ni ore 30–50 m thick with an average Ni grade of ~1% was formed at the R?anovo deposit; this layer is traced for more than 4 km along the strike and 500 m down the dip. At the end of the Late Cretaceous, intense Alpine tectonic faulting and folding resulted in overturning of the initially horizontal ore layer, which is now nearly vertical. The most abundant fissile hematite ore contains 0.70–1.27% Ni, whereas the economically most important massive hematite ore with 0.93–1.49% Ni occurs locally. The major Ni-bearing minerals are magnetite, hematite, chromite, sulfides, talc, chlorite, amphibole, and stilpnomelane.  相似文献   

10.
The Taojiang Mn ore deposit was exploited in the early 1960s, and waste rocks were developed since then. Because the Mn ores were hosted within the metal-enriched black shales (Peng et al., 2004), the continuous mining has led to the exposure of an immense quality of black shales, which might cause serious impacts on environments. The present study deals with this environmental issue with samples from the waste rocks, and from the surrounding soils and surface water. The mineralogy of the waste rock was studied using EMPA, then a large number of elements in all waste rock, soil, and water samples were analyzed at a wide range of concentrations with high accuracy using an Elan6000 ICP-MS machine at Guangzhou Institute of Geochemistry, Chinese Academy of Sciences. The waste rock is composed mostly of black shales, with minor Mn carbonates. Both black shales and Mn carbonates of the waste rock contain many sulfide minerals, mainly pyrite, with minor galena, sphalerite, chalcopyrite, and others. The waste rocks are enriched in many metals including Sc, V, Cr, Co, Ni, Fe, Mn, Cu, Zn, Pb, Th, U, Mo, Sb, Sn, Tl, and others, and the metals are mostly hosted within the sulfides. Weathering of waste rocks might cause emission of the following metals: V, Cd, Ni, Th, U, Mo, Sb, Tl, Sc, Cr, Cu, Zn, Sn, and minor Co, and Pb. The surrounding soils are highly enriched in Cr, Co, Cu, Zn, Mn, Mo, Cd, Tl, and Pb, with the enrichment factors of 2.67.3.8, 7.26, 7.27, 8.2, 5.7, 13, and 5.4, respectively. The element ratios (Rb/Cs, Fe/Mn, Nb/Zr, Hf/Zr, and Ba/Sr) and REE distribution patterns of the soils are similar to those of the waste rocks and bedrocks.  相似文献   

11.
New data on the Paleozoic Ol’cha gold-silver deposit are given, including interpretation of its tectonic setting and mineralogical characteristization, the most complete to date. Strike-slip deformation is crucial for the formation of the ore field structure.  相似文献   

12.
The Zijinshan high-sulfidation epithermal Cu–Au deposit is located in the Zijinshan ore field of South China, comprising porphyry–epithermal Cu–Au–Mo–Ag ore systems. The Cu ore body is more than 1000 m thick and is characterized by an assemblage of digenite–covellite–enargite–alunite. Digenite is the dominant Cu-bearing mineral, which makes this deposit unique, although the mechanisms of digenite formation remain controversial. To elucidate the genesis of digenite, this paper presents the Cu isotopic compositions of Cu-sulfides in the Zijinshan high-sulfidation Cu–Au deposit. The Cu isotopic values (65Cu relative to NIST 976) of all samples range from −2.97‰ to +0.34‰, and most values fall in a narrow range from −0.49‰ to +0.34‰, which is similar to the Cu isotopic signature of typical porphyry systems. Copper isotope ratios of each mineral decrease with increasing depth, a trend that is also typical of porphyry deposits. The variation tendency of δ65Cu values between sulfides is consistent with the sequence of mineral formation. These observations suggest that the Cu-sulfides in the Zijinshan Cu–Au deposit have a hypogene origin.  相似文献   

13.
Greenish veins occurring in brecciated bentonite were found in the Kawasaki bentonite deposit of the Zao region in Miyagi Prefecture, Japan. Their occurrence possibly indicates the interaction of bentonite with Fe-rich hydrothermal solutions. In order to prove the hypothesis and understand the long-term mineralogical and petrographic evolution of bentonite during such interactions, the greenish veins and the surrounding altered bentonite were analyzed using X-ray fluorescence (XRF), scanning electron microscopy (SEM), X-ray diffraction (XRD), electron probe micro-analysis (EPMA), scanning transmission electron microscopy with energy dispersed spectroscopy (STEM-EDS) and micro X-ray absorption near-edge structure (XANES). The greenish veins resulting from hydrothermal solution are composed of mixed-layer minerals consisting of smectite and glauconite (glaucony), pyrite and opal. The occurrences indicate that glaucony and pyrite formed almost simultaneously from hydrothermal solution prior to opal precipitation. The mineral assemblages of the greenish veins and their surroundings indicate that the hydrothermal activity had most likely taken place at a temperature of less than 100 °C and that the pH and Eh conditions of the reacted solution were neutral to alkaline pH and reducing. The unaltered bentonite is composed mainly of Al smectite and opal. These minerals coexist as a mixture within the resolution level of the microprobe analyses. On the other hand, the bentonite in contact with the greenish veins consists of discrete opal grains and dioctahedral Al smectite containing Fe and was altered mineralogically and petrographically by the hydrothermal activity. Both the clay minerals and the opal were formed by dissolution and subsequent precipitation from the interaction of the original bentonite with the hydrothermal solution.  相似文献   

14.
The Boliden deposit (8.3 Mt at 15.9 g/t Au) is interpreted to have been formed between ca. 1894 and 1891 Ma, based on two new U–Pb ID-TIMS ages: a maximum age of 1893.9?+?2.0/?1.9 Ma obtained from an altered quartz and feldspar porphyritic rhyolite in the deposit footwall in the volcanic Skellefte group and a minimum age of 1890.8?±?1 Ma obtained from a felsic mass-flow deposit in the lowermost part of the volcano-sedimentary Vargfors group, which forms the stratigraphic hanging wall to the deposit. These ages are in agreement with the alteration and mineralization being formed at or near the sea floor in the volcanogenic massive sulfide environment. These two ages and the geologic relationships imply that: (1) volcanism and hydrothermal activity in the Skellefte group were initiated earlier than 1.89 Ga which was previously considered to be the onset of volcanism in the Skellefte group; (2) the volcano-sedimentary succession of the Vargfors group is perhaps as old as 1892 Ma in the eastern part of the Skellefte district; and (3) an early (synvolcanic) deformation event in the Skellefte group is evidenced by the unconformity between the ≤1893.9?+?2.0/?1.9 Ma Skellefte group upper volcanic rocks and the ≤1890.8?±?1 Ma Vargfors sedimentary and volcanic rocks in the Boliden domain. Differential block tilting, uplift, and subsidence controlled by synvolcanic faults in an extensional environment is likely, perhaps explaining some hybrid VMS-epithermal characteristics shown by the VMS deposits of the district.  相似文献   

15.
Hydrothermal alteration and mineralization at the Wunugetu porphyry Cu–Mo deposit, China, include four stages, i.e., the early stage characterized by quartz, K-feldspar and minor mineralization, followed by a molybdenum mineralization stage associated with potassic alteration, copper mineralization associated with sericitization, and the last Pb–Zn mineralization stage associated with carbonation. Hydrothermal quartz contains three types of fluid inclusions, namely aqueous (W-type), daughter mineral-bearing (S-type) and CO2-rich (C-type) inclusion, with the latter two types absent in the late stage. Fluid inclusions in the early stage display homogenization temperatures above 510°C, with salinities up to 75.8 wt.% NaCl equivalent. The presence of S-type inclusions containing anhydrite and hematite daughter minerals and C-type inclusions indicates an oxidizing, CO2-bearing environment. Fluid inclusions in the Mo- and Cu-mineralization stages yield homogenization temperatures of 342–508°C and 241–336°C, and salinities of 8.6–49.4 and 6.3–35.7 wt.% NaCl equivalent, respectively. The presence of chalcopyrite instead of hematite and anhydrite daughter minerals in S-type inclusions indicates a decreasing of oxygen fugacity. In the late stage, fluid inclusions yield homogenization temperatures of 115–234°C and salinities lower than 12.4 wt.% NaCl equivalent. It is concluded that the early stage fluids were CO2 bearing, magmatic in origin, and characterized by high temperature, high salinity, and high oxygen fugacity. Phase separation occurred during the Mo- and Cu-mineralization stages, resulting in CO2 release, oxygen fugacity decrease and rapid precipitation of sulfides. The late-stage fluids were meteoric in origin and characterized by low temperature, low salinity, and CO2 poor.  相似文献   

16.
The pre-Cenozoic geology at Candelaria, Nevada comprises four main lithologic units: the basement consists of Ordovician cherts of the Palmetto complex; this is overlain unconformably by Permo-Triassic marine clastic sediments (Diablo and Candelaria Formations); these are structurally overlain by a serpentinitehosted tectonic mélange (Pickhandle/Golconda allochthon); all these units are cut by three Mesozoic felsic dike systems. Bulk-mineable silver-base metal ores occur as stratabound sheets of vein stockwork/disseminated sulphide mineralisation within structurally favourable zones along the base of the Pickhandle allochthon (i.e. Pickhandle thrust and overlying ultramafics/mafics) and within the fissile, calcareous and phosphatic black shales at the base of the Candelaria Formation (lower Candelaria shear). The most prominent felsic dike system — a suite of Early Jurassic granodiorite porphyries — exhibits close spatial, alteration and geochemical associations with the silver mineralisation. Disseminated pyrites from the bulk-mineable ores exhibit a 34S range from — 0.3 to + 12.1 (mean 34S = +6.4 ± 3.5, 1, n = 17) and two sphalerites have 34S of + 5.9 and + 8.7 These data support a felsic magmatic source for sulphur in the ores, consistent with their proximal position in relation to the porphyries. However, a minor contribution of sulphur from diagenetic pyrite in the host Candelaria sediments (mean 34S = — 14.0) cannot be ruled out. Sulphur in late, localised barite veins ( 34S = + 17.3 and + 17.7) probably originated from a sedimentary/seawater source, in the form of bedded barite within the Palmetto basement ( 34S = + 18.9). Quartz veins from the ores have mean 18O = + 15.9 ± 0.8 (1, n = 10), which is consistent, over the best estimate temperature range of the mineralisation (360°–460°C), with deposition from 18O-enriched magmatic-hydrothermal fluids (calculated 18O fluid = + 9.4 to + 13.9). Such enrichment probably occurred through isotopic exchange with the basement cherts during fluid ascent from a source pluton. Whole rock data for a propylitised porphyry ( 18O = + 14.2, D = — 65) support a magmatic fluid source. However, D results for fluid inclusions from several vein samples (mean = — 108 ± 14, 1, n = 6) and for other dike and sediment whole rocks (mean = — 110 ± 13, 1, n = 5) reveal the influence of meteoric waters. The timing of meteoric fluid incursion is unresolved, but possibilities include late-mineralisation groundwater flooding during cooling of the Early Jurassic progenitor porphyry system and/or meteoric fluid circulation driven by Late Cretaceous plutonism.  相似文献   

17.
This study investigates the major and trace element geochemistry of Bigadi borate deposits, the largest colemanite and ulexite deposits in the world. The known borate deposits of Turkiye were deposited in the lacustrine environment during Miocene when the volcanic activity occurred from Tertiary to Quaternary. All of the Turkish borate deposits are classified as volcanic related deposits. Boron ore deposits intercalated with claystone, mudstone, tufa and fine layered limestone show lens shape. Borate minerals formed in two zones. Tiilu and Acep-Simav open mines represented the lower and upper borate zones, respectively. Colemanite and ulexite are dominant minerals at all ore zones. The major elements of Bigadi borates contain Ca, Si, Mg, Al, Fe, S, Na, P and Mn at Tiilu, Ca, Na, Si, Mg, S, Al, P and Mn at Simav, and Ca, Na, Si, Mg, S, AI and Mn at Acep samples respectively. Except for Li, Mo, Sb, As, Sr and Se, concentrations of other trace elements are significantly lower than averages of earth crust and andesite at the three mines. With respect to averages of earth crust and andesite, Mo, Sr, As, Li and particularly Se are enriched significantly in the Bigadi. In examining depth-dependent variations of major and trace elements, four element groups at the Tiilu site and six element groups at the Simav and Acep sites were determined. Element abudances or element geochemical trends show differences at the Tülü, Simav and Acep mines. These differences can be explained by the diversity of physicochemical conditions in the deposition environment by the effect of differences at the recharge regime and source.  相似文献   

18.
The Zhazixi Sb–W deposit in the Xuefeng uplift, South China, exhibits a unique metal association of W and Sb, where the W orebodies are hosted by interlayer fractures and the Sb orebodies are contained within NW-trending faults. This study proposes that the W and Sb mineralization took place in two separate periods. The mineral paragenesis of the W mineralization reveals a mass of quartz, scheelite and minor calcite. The mineral assemblage of the Sb mineralization developed after W mineralization and consists of predominantly quartz and stibnite, and small amounts of native Sb, berthierite, chalcostibnite, pyrite, and chalcopyrite. Fluid inclusions in quartz and coexisting scheelite are dominated by two-phase, liquid-rich, aqueous inclusions at room temperature. Microthermometric studies suggest that ore-forming fluids for W mineralization are characterized by moderate temperatures (170–270 °C), low salinity (3–7 wt% NaCl equiv.), low density (0.75–0.95 g/cm3), and moderate to high pressure (57.2–99.7 MPa) and these fluids experienced a cooling and dilution evolution during W mineralization. Ore-forming fluids for Sb mineralization are epithermal types with low temperatures (150–230 °C), low salinity (4–6 wt% NaCl equiv.), moderate density (0.82–0.94 g/cm3), and high pressure (42.2–122.5 MPa) and these fluids display an evident decline in homogenization temperature during Sb mineralization. Laser Raman analyses of the vapor phase indicate that the ore-forming fluids for both W and Sb mineralization contain a small amount of CO2.The ore-forming fluids for Sb mineralization are identified as predominantly originating from the continental crust, as suggested by the low 3He values (0.009 × 10−12 cc.STP/g) and 3He/4He ratios (0.002–0.056 Ra) as well as high 36Ar values (1.93 × 10−9 cc.STP/g) and 40Ar/36Ar ratios (909.5–2279.7). The source of S is identified to be the Neoproterozoic Wuqiangxi Formation, as traced by the δ34SV-CDT values of stibnite (3.1–9.4‰). The 208Pb/204Pb (37.643–40.222), 207Pb/204Pb (15.456–15.681), and 206Pb/204Pb (17.093–20.042) ratios suggest a mixture of lower crustal and supracrustal Pb sources.It is thus concluded that the ore genesis of the Zhazixi Sb–W deposit is related to the intracontinental orogeny during the early Mesozoic. Fluid mixing is considered to be the critical mechanism involved in W mineralization, whereas a fluid cooling process is responsible for Sb mineralization. Furthermore, the absence of Au is attributed to the low Σas content in Sb-mineralizing fluids.  相似文献   

19.
1 Introduction Alunite [KAl3(SO4)2(OH)6] is a very important non-ferrous metal resource, so many countries throughout the world have made great investments in research on the mechanism of its formation, its geological characteristics and applications. O…  相似文献   

20.
The Zhaima gold–sulfide deposit is located in the northwestern part of the West Kalba gold belt in eastern Kazakhstan. The mineralization is hosted in Lower Carboniferous volcanic and carbonate rocks formed under conditions of marginal-sea and island-arc volcanic activity. The paper considers the mineralogy and geochemistry of primary gold–sulfide ore and Au-bearing weathering crusts. Au-bearing arsenopyrite–pyrite mineralization formed during only one productive stage. Disseminated, stringer–disseminated, and massive rocks are enriched in Ti, Cr, V, Cu, and Ni, which correspond to the mafic profile of basement. The main ores minerals are represented by finely acicular arsenopyrite containing Au (up to few tens of ppm) and cubic and pentagonal dodecahedral pyrite with sporadic submicroscopic inclusions of native gold. The sulfur isotopic composition of sulfides is close to that of the meteoritic standard (δ34S =–0.2 to +0.2). The 40Ar/39Ar age of three sericite samples from ore veinlets corresponds to the Early Permian: 279 ± 3.3, 275.6 ± 2.9, and 272.2 ± 2.9 Ma. The mantle source of sulfur, ore geochemistry, and spatial compatibility of mineralization with basic dikes allow us to speak about the existence of deep fluid–magmatic systems apparently conjugate with the Tarim plume.  相似文献   

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