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1.
Re-Os isotopes were used to constrain the source of the ore-forming elements of the Tharsis and Rio Tinto mines of the Iberian Pyrite Belt, and the timing of mineralization. The pyrite from both mines has simila]r Os and Re concentrations, ranging between 0.05–0.7 and 0.6–66 ppb, respectively. 187Re/188Os ratios range from about 14 to 5161. Pyrite-rich ore samples from the massive ore of Tharsis and two samples of stockwork ore from Rio Tinto yield an isochron with an age of 346 ± 26 Ma, and an initial 187Os/188Os ratio of about 0.69. Five samples from Tharsis yield an age of 353 ± 44 Ma with an initial 187Os/188Os ratio of about 0.37. A sample of massive sulfide ore from Tharsis and one from Rio Tinto lie well above both isochrons and could represent Re mobilization after mineralization. The pyrite Re-Os ages agree with the paleontological age of 350 Ma of the black shales in which the ores are disseminated. Our data do not permit us to determine whether the Re-Os isochron yields the original age of ore deposition or the age of the Hercynian metamorphism that affected the ores. However, the reasonable Re-Os age reported here indicates that the complex history of the ores that occurred after the severe metamorphic event that affected the Iberian Pyrite Belt massive sulfide deposits did not fundamentally disturb the Re-Os geochronologic system. The highly radiogenic initial Os isotopic ratio agrees with previous Pb isotopic studies. If the initial ratio is recording the initial and not the metamorphic conditions, then the data indicate that the source of the metals was largely crustal. The continental margin sediments that underlie the deposits (phyllite-quartzite group) or the volcanic rocks (volcanogenic-sedimentary complex) in which the ores occur are plausible sources for the ore-forming metals and should constrain the models for the genesis of these deposits. Received: 15 March 1999 / Accepted: 26 July 1999  相似文献   

2.
The Kalyadi polymetallic copper deposit occurs within the Middle Archaean (≥3.0 Ga), medium-grade Kalyadi schist belt which consists predominantly of ultramafic-mafic schists interbedded with chemogenic chert, detrital high Al-Mg schists and siliceous schists. This sedimentary exhalative type (SEDEX type) ore-body is the only copper deposit hosted in cherts in the western Dharwar craton. The Kalyadi supracrustal rocks are intruded by tonalite-trondhjemitic gneisses (ca. 3.0 Ga) and granite (ca. 2.6 Ga). The Kalyadi copper deposit is polygenetic in nature. The primary ores represented by disseminations of pyrite ± linneite and chalcopyrite ± magnetite essentially along the bedding lamination of the metachert are referred to as the metamorphosed chert-sulphide rhythmites of a primary stratiform type. The ore is of low-grade and records imprints of at least two events of deformation. Pyrite is characterised by high-Co values (262–4524 ppm) and high–Co/Ni ratios (3.0–19.7). Rare earth element patterns of the primary ores and the host metacherts are identical, characterised by La enrichment, absence of Eu anomalies and flat to depleted HREE patterns with δ 34 S = −0.8‰. The secondary (remobilised) ores are structurally controlled occurring as veins and stringers discordant to the bedding lamination or schistosity. The constituent ores are chalcopyrite-pyrite-pyrrhotite with minor pentlandite. These sulphides with low-Co/Ni ratios (0.87–1.80), have either a strong positive or negative Eu anomaly and show slight HREE enrichment. The δ 34 S value ranges from +2.64 to −4.29‰. It is interpreted that the primary stratiform ores and the cherts were derived from volcanogenic hydrothermal fluids as syngenetic/chemical deposits in a deep sea environment. The secondary epigenetic mineralisation is related to subsequent migmatisation, deformational events and granitic activity. Received: 8 September 1995 / Accepted: 18 November 1996  相似文献   

3.
The ~260 Ma-old Baimazhai Ni–Cu–(PGE) sulfide deposit in the Jinping region, Yunnan, SW China, is hosted in a small mafic–ultramafic intrusion, which intruded Ordovician sandstone and slate. The intrusion is concentric with lens shape, about 530 m long, 190 m wide and 24 to 64 m thick, trends 296°, and dips 22°NE. The massive sulfide ore body forms the core of the intrusion and is surrounded by variably mineralized orthopyroxenite, websterite and barren gabbro. The proportion of gabbro, websterite, orthopyroxenite and massive ore is approximately 30, 30, 20 and 20 vol.%, respectively. Magmatic pyrrhotite, pentlandite and chalcopyrite make up more than 90% of the massive ores. The massive ores contain high Ni (1.6 to 4.2 wt%) and Cu (0.4 to 6.5 wt%) and low ∑PGE contents (85 to 524 ppb). They have Pd/Ir ratios ranging from 6.7 to 530, Pd/Pt ratios from 0.7 to 2.6 and Cu/(Pd×1,000) ratios from 31 to 400, which are comparable with those of the silicate rocks [Pd/Ir = 4 to 183, Pd/Pt = 0.7 to 3.5, and Cu/(Pd×1,000) = 100 to 400]. Similar Pd/Pt and Cu/Pd ratios of the silicate rocks and massive ores throughout the intrusion indicate a single sulfide segregation event. Excess sulfide melt segregation resulted from intensive crustal contamination that formed Si-rich and Mg-rich basaltic magmas in a deep-seated staging chamber before magma emplacement. The immiscible sulfide melts and the silicate melts were eventually evacuated from the staging magma chamber by compressive forces. Flow differentiation under high velocity concentrated the sulfide melts toward the middle of the magma flow, and consequently, formed a massive sulfide ore body in the central part of the intrusion. Low concentrations of PGEs and general absence of platinum-group minerals in the massive ores may have resulted from a relatively large mass fraction of the sulfide melts (e.g. R-factor = ~70) in Baimazhai compared with other intrusions elsewhere, such as Noril’sk-Talnakh with a R-factor of >10,000.  相似文献   

4.
The Otavi Mountain Land is a base metal sulphide ore province in northern Namibia where deposits are hosted by platform carbonates of the Otavi Group in a foreland fold-and-thrust belt on the northern edge of the Pan-African Damara Belt. Deposits have been classified as the Berg Aukas- or Tsumeb-types, based on differences in ore association, stratigraphic position and geochemistry of ores and gangue carbonates. Mineralisation at these deposits is accompanied by carbonate alteration in the form of dolomite and calcite veins, carbonate recrystallisation, calcitisation and carbonate silicification. Based on cathodoluminescence imaging, trace and rare earth element (REE), O and C isotope, and fluid inclusion data, a series of carbonate generations, constituting wall rock alteration around the Tsumeb and Kombat (Tsumeb-type) and Berg Aukas (Berg Aukas-type) deposits, was established. Similar data obtained on the recently discovered Khusib Springs deposit indicate a strong affinity to Tsumeb-type deposits. Tsumeb-type deposits are distinguished from Berg Aukas-type deposits by having trace element and REE concentrations that are significantly higher in the alteration products compared to the carbonate host rocks. Only around Tsumeb-type deposits a relative enrichment in light REE is noted for the hydrothermal carbonate generations that are cogenetic with the main stage of mineralisation. Microthermometric results from fluid inclusions in carbonate alteration phases and associated quartz indicate relatively high salinity (17–23 wt% NaCl equivalent) for the main mineralising and subsequent sulphide remobilisation stages at the deposits investigated. Estimated mineralisation temperatures are significantly higher for Tsumeb-type deposits (370–405 °C) with early sulphide remobilisation in Tsumeb at 275 °C, whereas they are lower at Berg Aukas (up to 255 °C). Fluid inclusion leachate analysis suggests that most of the observed salinity can be ascribed to dissolved, predominantly Ca- and Mg-carbonates and chlorides with subordinate NaCl. Na-Cl-Br leachate systematics indicate a derivation of the fluid salinity from the interaction with evaporitic rocks en route. Tsumeb-type mineralisation is interpreted to be derived from fluids expelled during Pan-African orogeny in the more intensely deformed internal zones of the Damara Belt further south. When the high salinity fluids reached the carbonate platform after having scavenged high concentrations of base metals, base metal sulphide precipitation occurred in zones of high porosity, provided by karst features in the carbonate sequence. Results obtained for the Berg Aukas-type deposits emphasise their derivation from basinal brines, similar to Mississippi Valley-type deposits, and confirm that mineralisation of the Berg Aukas- and Tsumeb-types are both spatially and temporally distinct. Received: 5 May 1999 / Accepted: 10 November 1999  相似文献   

5.
We studied a number of magmatic Ni–Cu–(PGE) sulfide deposits in two distinct belts in eastern Botswana. The Tati belt contains several relatively small deposits (up to 4.5 Mt of ore at 2.05% Ni and 0.85% Cu) at Phoenix, Selkirk and Tekwane. The deposits are hosted by ca 2.7 Ga, low- to medium-grade metamorphosed gabbroic–troctolitic intrusions situated within or at the periphery of a greenstone belt. The deposits of the Selebi-Phikwe belt are larger in size (up to 31 Mt of ore grade). They are hosted by high-grade metamorphosed gabbronorites, pyroxenites and peridotites believed to be older than ca 2.0 Ga that intruded gneisses of the Central Zone of the Limpopo metamorphic belt. The composition of the sulfide mineralisation in the two belts shows systematic variation. Most of the mineralisation in the Tati belt contains 2–9% Ni and 0.05–4% Cu (Cu/Cu + Ni = 0.4–0.7), whereas most of the mineralisation in the Selebi-Phikwe belt contains 1–3% Ni and 0.1–4% Cu (Cu/Cu + Ni = 0.4–0.9). The Cu–Ni tenors of the ores in both belts are consistent with crystallization from a basaltic magma. The Tati ores contain mostly >3 ppm Pt + Pd (Pt/Pd 0.1–1), with Pd/Ir = 100–1,000, indicative of a differentiated basaltic magma that remained S-undersaturated before emplacement. Most of the Selebi-Phikwe ores have <0.5 ppm Pt + Pd (Pt/Pd < 0.1–1), with Pd/Ir = 10–500. This suggests a relatively less differentiated magma that reached S saturation before emplacement. The Tati rocks show flat mantle-normalised incompatible trace element patterns (average Th/YbN = 1.57), except for strong enrichments in large ion lithophile elements (Cs, Rb, Ba, U, K). Such patterns are characteristic of relatively uncontaminated oceanic arc magmas and suggest that the Tati intrusions were emplaced in a destructive plate margin setting. Most of the Selebi-Phikwe rocks (notably Dikoloti) have more fractionated trace element signatures (average Th/YbN = 4.22), possibly indicating digestion of upper crustal material during magma emplacement. However, as there are also samples that have oceanic arc-like signatures, an alternative possibility is that the composition of most Selebi-Phikwe rocks reflects tectonic mingling of the intrusive rocks with the country rocks. The implication is that orogenic belts may have a higher prospectivity for magmatic Ni–Cu ores than presently recognised. The trigger mechanism for sulfide saturation and segregation in all intrusions remains unclear. Whereas the host rocks to the intrusions appear to be relatively sulfur poor, addition of crustal S to the magmas is suggested by low Se/S ratios in some of the ores (notably at Selebi-Phikwe). External S sources may thus remain unidentified due to poor exposure and/or S mobility in response to metamorphism.  相似文献   

6.
Lead isotope ratios of galena from the carbonate-hosted massive sulphide deposits of Kabwe (Pb-Zn) and Tsumeb (Pb-Zn-Cu) in Zambia and Namibia, respectively, have been measured and found to be homogeneous and characteristic of upper crustal source rocks. Kabwe galena has average isotope ratios of 206/204Pb = 17.997 ± 0.007, 207/204Pb = 15.713 ± 0.010 and 208/204Pb = 38.410 ± 0.033. Tsumeb galena has slightly higher 206/204Pb (18.112 ± 0.035) and slightly lower 207/204Pb (15.674 ± 0.016) and 208/204Pb (38.276 ± 0.073) ratios than Kabwe galena. The isotopic differences are attributed to local differences in the age and composition of the respective source rocks for Kabwe and Tsumeb. The homogeneity of the ore lead in the two epigenetic deposits suggests lead sources of uniform isotopic composition or, alternatively, thorough mixing of lead derived from sources with relatively similar isotopic compositions. Both deposits have relatively high 238U/204Pb ratios of 10.31 and 10.09 for Kabwe and Tsumeb galenas, respectively. These isotope ratios are considered to be typical of the upper continental crust in the Damaran-Lufilian orogenic belt, as also indicated by basement rocks and Cu-Co sulphides in stratiform Katangan metasediments which have a mean μ-value of 10.25 ± 0.12 in the Copperbelt region of Zambia and the Democratic Republic of Congo (formerly Zaire). The 232Th/204Pb isotope ratios of 43.08 and 40.42 for Kabwe and Tsumeb suggest Th-enriched source regions with 232Th/235U (κ-values) of 4.18 and 4.01, respectively. Model isotopic ages determined for the Kabwe (680 Ma) and Tsumeb (530 Ma) deposits indicate that the timing of the mineralisation was probably related to phases of orogenic activity associated with the Pan-African Lufilian and Damaran orogenies, respectively. Galena from the carbonate-hosted Kipushi Cu-Pb-Zn massive sulphide deposit in the Congo also has homogeneous lead isotope ratios, but its isotopic composition is comparable to that of the average global lead evolution curve for conformable massive sulphide deposits. The μ (9.84) and κ (3.69) values indicate a significant mantle component, and the isotopic age of the Kipushi deposit (456 Ma) suggests that the emplacement of the mineralisation was related to a post-tectonic phase of igneous activity in the Lufilian belt. The isotope ratios (206/204Pb, 207/204Pb, 208/204Pb) of the three deposits are markedly different from the heterogeneous lead ratios of the Katangan Cu-Co stratiform mineralisation of the Copperbelt as well as those of the volcanogenic Nampundwe massive pyrite deposit in the Zambezi belt which typically define radiogenic linear trends on lead-lead plots. The host-rock dolomite of the Kabwe deposit also has homogeneous lead isotope ratios identical to the ore galena. This observation indicates contamination of the Kabwe Dolomite Formation with ore lead during mineralisation. Received: 8 September 1997 / Accepted: 21 August 1998  相似文献   

7.
Summary The Dachang Sn-polymetallic ore district is one of the largest tin producing districts in China. Its origin has long been in dispute between magmatic-hydrothermal replacement and submarine exhalative-hydrothermal origin. The Dachang ore district comprises several types of ore deposits, including the Lamo magmatogenic skarn deposit near a granite intrusion, the Changpo-Tongkeng bedded and vein-type sulfide deposit, and the Gaofeng massive sulfide deposit. Sulfide minerals from the Lamo skarn ores show δ34S values in the range between −3 and +4‰ with a mean close to zero, suggesting a major magmatic sulfur source that likely was the intrusive Longxianggai granite. Sulfide minerals from the Gaofeng massive ores show higher δ34S values between +5 and +12‰, whereas sulfide minerals from the Changpo-Tongkeng bedded ores display lighter δ34S values between −7 and −0.2‰. The difference in the sulfur isotope ranges in the two deposits can be interpreted by different degrees of inorganic thermochemcial reduction of marine sulfate using a one-step batch separation fractionation model. Sulfur isotopic compositions from the vein-type ores at Changpo-Tongkeng vary widely from −8 to +4‰, but most of the data cluster around −2.9‰, which is close to that of bedded ores (−3.6‰). The sulfur in vein-type ores might be derived from bedded ores or it represents a mixture of magmatic- and sedimentary-derived sulfur. Pb isotopic compositions of sulfide minerals in the Dachang ore district reveal a difference between massive and bedded ores, with the massive ores displaying more radiogenic Pb isotope ratios. Correlations of 206Pb/204Pb and 207Pb/204Pb or 208Pb/204Pb for the massive and bedded ores are interpreted as two-component mixing of Pb leached from sedimentary host rocks and from deep-seated Precambrian basement rocks composed of metamorphosed volcano-sedimentary rocks. Pb isotopic compositions of sulfide minerals from vein-type ores overlap with those of bedded sulfides. Similar to the sulfur, the lead in vein-type ores might be derived from bedded ores. Skarn ores at Lamo show very limited variations in Pb isotopic compositions, which may reflect a major magmatic-hydrothermal lead source. Helium isotope data of fluid inclusions trapped in sulfides indicate that He in the massive and bedded ores has a different origin than He in fluorite of granite-related veins. The 3He/4He ratios of 1.2–2.9 Ra of fluid inclusions from sulfides at Gaofeng and Changpo-Tongkeng imply a contribution of mantle-derived fluids. Overall our data support a submarine exhalative-hydrothermal origin for the massive and bedded ore types at Dachang. Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material  相似文献   

8.
Summary ?The Yunlong tin deposit is located in the northern part of the Lancangjiang metamorphic zone of the Sanjiang Tethys orogen series in western Yunan province of China. It consists of vein-type cassiterite ores, which are mainly hosted in migmatites of Caledonian age. Abundant tourmaline is associated with the ores, quartz–tourmaline veins and barren migmatized gneiss and migmatites. A detailed electron microprobe study has been carried out to document the chemical compositions of tourmaline from this deposit. The results exhibit a systematic compositional change that might be used as tracer for ore genesis and in prospecting for tin mineralization. Tourmalines from the ore bodies are dravite with Fe/(Fe + Mg) ratios of 0.09 ∼ 0.31 and Ca/(Ca + Na) ratios of 0.03 ∼ 0.40. These tourmalines are also rich in chromium (up to 0.74 wt% Cr2O3) and tin (up to 0.42 wt% Sn). In contrast, tourmalines from the barren migmatites are mostly schorl with Fe/(Fe + Mg) ratios of 0.38 ∼ 0.94 and Ca/(Ca + Na) ratios of 0.00 ∼ 0.14. Tourmalines from quartz–tourmaline veins that occur between ore bodies and the migmatites show intermediate compositions, i.e., Fe/(Fe + Mg) = 0.09 ∼ 0.59, Ca/(Ca + Na) = 0.01 ∼ 0.22. It is suggested that the Mg-rich nature of the tourmaline can be used as an exploration tool in this region to target tin mineralization, because the tourmalines show increasing Mg contents and are more dravitic when approaching the ore bodies. It is likely that the formation of the Yunlong tin deposit was related to migmatitic-hydrothermal processes. The high Mg and Cr contents in tourmalines from the ore bodies were probably derived from the local meta-sedimentary and meta-volcanic rocks of the Precambian Chongshan Group rather than from the granites in the region. Received December 28, 2000; revised version accepted January 25, 2002  相似文献   

9.
Summary The Jinchuan deposit is a platinum group element (PGE)-rich sulfide deposit in China. Drilling and surface sampling show that three categories of platinum group element (PGE) mineralization occur; type I formed at magmatic temperatures, type II occurs in hydrothermally altered zones of the intrusion, and type III in sheared dunite and lherzolite. All ore types were analyzed for Os, Ir, Ru, Rh, Pd, Pt and Au, as well as for Cu, Ni, Co and S. Type I ore has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios of <7 and relatively flat chondrite-normalized noble metal patterns; the platinum group minerals (PGM) are dominated by sperrylite and moncheite associated with chalcopyrite, pyrrhotite and pentlandite. Type II has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 40 to 330 and noble metal distribution patterns with a positive slope; the most common PGM are sperrylite and Pd bismuthotelluride phases concentrated mostly at the margins of base metal sulfides. Type III ores have the highest (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 240 to 710; the most abundant PGM are sperrylite and phases of the Pt–Pd–Te–Bi–As–Cl system. It is concluded that the Jinchuan deposit formed as a result of primary magmatic crystallization followed by hydrothermal remobilization, transport, and deposition of the PGE.  相似文献   

10.
The Iberian type of volcano-sedimentary massive sulphide deposits   总被引：6，自引：0，他引：6  
The Iberian Pyrite Belt, located in the SW Iberian Peninsula, contains many Paleozoic giant and supergiant massive sulphide deposits, including the largest individual massive sulphide bodies on Earth. Total ore reserves exceed 1500 Mt, distributed in eight supergiant deposits (>100 Mt) and a number of other smaller deposits, commonly with associated stockwork mineralizations and footwall alteration haloes. Massive sulphide bodies largely consist of pyrite, with subordinated sphalerite, galena and chalcopyrite and many other minor phases, although substantial differences occur between individual deposits, both in mineral abundance and spatial distribution. These deposits are considered to be volcanogenic, roughly similar to volcanic-hosted massive sulphides (VHMS). However, our major conclusion is that the Iberian type of massive sulphides must be considered as a VHMS sub-type transitional to SHMS. This work is an assessment of the geological, geochemical and metallogenic data available up to date, including a number of new results. The following points are stressed; (a) ore deposits are located in three main geological sectors, with the southern one containing most of the giant and supergiant orebodies, whereas the northern one has mainly small to intermediate-sized deposits; (b) ore deposits differ one from another both in textures and mineral composition; (c) Co and Bi minerals are typical, especially in stockwork zones; (d) colloidal and other primary depositional textures are common in many localities; (e) a close relation has been found between ore deposits and some characteristic sedimentary horizons, such as black shales. In contrast, relationships between massive sulphides and cherts or jaspers remains unclear; (f) footwall hydrothermal alterations show a rough zoning, the inner alteration haloes being characterized in places by a high Co/Ni ratio, as well as by mobility of Zr, Y and REE; (g) 18O and D values indicate that fluids consist of modified seawater, whereas 34S data strongly suggest the participation of bacterial-reduced sulphur, at least during some stages of the massive sulphide genesis, and (h) lead isotopes suggest a single (or homogeneized) metal source, from both the volcanic piles and the underlying Devonian rocks (PQ Group). It is concluded that, although all these features can be compatible with classical VHMS interpretations, it is necessary to sketch a different model to account for the IPB characteristics. A new proposal is presented, based on an alternative association between massive sulphide deposits and volcanism. We consider that most of the IPB massive orebodies, in particular the giant and supergiant ones, were formed during pauses in volcanic activity, when hydrothermal activity was triggered by the ascent and emplacement of late basic magmas. In these conditions, deposits formed which had magmatic activity as the heat source; however, the depositional environment was not strictly volcanogenic, and many evolutionary stages could have occurred in conditions similar to those in sediment-hosted massive sulphides (SHMS). In addition, the greater thickness of the rock pile affected by hydrothermal circulation would account for the enormous size of many of the deposits. Received: 8 September 1998 / Accepted: 4 January 1999  相似文献   

11.
We present 40Ar/39Ar data acquired by infra-red (CO2) laser step-heating of alunite crystals from the large Miocene Colquijirca district in central Peru. Combined with previously published data, our results show that a long (at least 1.3 My) and complex period of magmatic-hydrothermal activity associated with epithermal Au–(Ag) mineralization and base metal, Cordilleran ores took place at Colquijirca. The new data indicate that incursion of magmatic SO2-bearing vapor into the Colquijirca epithermal system began at least as early as ∼11.9 Ma and lasted until ∼10.6 Ma. Four alunite samples associated with high-sulfidation epithermal Au–(Ag) ore gave 40Ar/39Ar plateau ages between ∼11.9 and ∼11.1 Ma (compared to the previously documented ∼11.6 to ∼11.3 Ma). By combining individually these new ages with crosscutting relationships, the duration of the Au–(Ag) deposition period can be estimated to at least 0.4 My. Three new 40Ar/39Ar plateau ages on alunite associated with the base-metal Cordilleran ores are consistent with previously obtained ages, all of them between 10.83 ± 0.06 and 10.56 ± 0.06 Ma, suggesting that most of the sulfide-rich polymetallic deposits of Smelter and Colquijirca formed during this short period. The recognition of consecutive alunite-bearing and alunite-free mineral assemblages within both the Au–(Ag) and the base-metal Cordilleran ores may suggest that SO2-bearing magmatic vapor entered the epithermal environment as multiple discontinuous pulses, a number of which was not necessarily associated in time with ore fluids. It is likely that a period of SO2-bearing vapor degassing longer than 11.9 to 10.6 Ma may be recognized with further more detailed work. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

12.
Vein-type tin mineralization in the Dadoushan deposit, Laochang ore field, Gejiu district, SW China, is predominantly hosted in Triassic carbonate rocks (Gejiu Formation) over cupolas of the unexposed Laochang equigranular granite intrusion. The most common vein mineral is tourmaline, accompanied by skarn minerals (garnet, diopside, epidote, phlogopite) and beryl. The main ore mineral is cassiterite, accompanied by minor chalcopyrite, pyrrhotite, and pyrite, as well as scheelite. The tin ore grade varies with depth, with the highest grades (~1.2 % Sn) prevalent in the lower part of the vein zone. Muscovite 40Ar–39Ar dating yielded a plateau age of 82.7 ± 0.7 Ma which defines the age of the vein-type mineralization. Measured sulfur isotope compositions (δ 34S = −4.1 to 3.9 ‰) of the sulfides (arsenopyrite, chalcopyrite, pyrite, and pyrrhotite) indicate that the sulfur in veins is mainly derived from a magmatic source. The sulfur isotope values of the ores are consistent with those from the underlying granite (Laochang equigranular granite, −3.7 to 0.1 ‰) but are different from the carbonate wall rocks of the Gejiu Formation (7.1 to 11.1 ‰). The calculated and measured oxygen and hydrogen isotope compositions of the ore-forming fluids (δ 18OH2O = −2.4 to 5.5 ‰, δD = −86 to −77 ‰) suggest an initially magmatic fluid which gradually evolved towards meteoric water during tin mineralization.  相似文献   

13.
The Kabanga deposit constitutes one of the most significant Ni sulfide discoveries of the last two decades (indicated mineral resource 23 Mt of ore at 2.64% Ni, inferred resource 28.5 Mt at 2.7% Ni, November 2008). The sulfides are hosted by predominantly harzburgitic and orthopyroxenitic intrusions that crystallized from magnesian basaltic and picritic magmas. However, compared with other sulfide ores that segregated from such magmas (e.g., Jinchuan, Pechenga, Raglan), most Kabanga sulfides have low Ni (<1–3%), Cu (∼0.1–0.4%), and PGE contents (≪1 ppm), high Ni/Cu (5–15), and low Ni/Co (10–15) and Pd/Ir (2–20). Sulfides with higher metal contents (up to ∼5% Ni, 0.8% Cu, 10 ppm PGE) are found in only one unit from Kabanga North. The observed metal contents are consistent with segregation of magmatic sulfides from fertile to strongly metal-depleted magmas, at intermediate to very low mass ratios of silicate to sulfide liquid (R factors) of approximately 10–400. Sulfide saturation was triggered prior to final emplacement, by assimilation of up to 50% of the total sulfur in the intrusions from sulfide-bearing metasedimentary country rocks. Immiscible sulfide liquid was entrained by the magma and ultimately precipitated in dynamic magma conduits that formed tubular and sill-like mafic–ultramafic bodies characterized by abundant magmatic breccias, highly irregular layering, and frequent compositional reversals. The unusually large degree of crustal contamination and the low R factors render Kabanga an end-member in the spectrum of magmatic Ni sulfide ores.  相似文献   

14.
The stratiform sulphide and oxide ores of Bergslagen, south-central Sweden, constitute the largest concentration of base metal and iron ores in northern Europe. They are hosted by Early Proterozoic metamorphosed volcanic and sedimentary successions, which (together with later granitoids) belong to the Svecofennian Domain. An earlier genetic model suggested that two principal types of sulphide ores existed in Bergslagen (Falun and Åmmeberg), which had been formed through two contrasting granitoid-related processes, whereas the iron oxide ores were considered exhalative-volcanogenic. The prevailing view for the Bergslagen ores is that all stratiform sulphide (and oxide) ores were formed by exhalative-volcanogenic processes from one homogenous metal source. In this paper are presented new high-precision determinations of the ore lead isotopic composition of twentytwo stratiform sulphide and oxide ores in Bergslagen (among them Falun, Zinkgruvan-Åmmeberg and Dannemora), in order to provide an improved base for their genesis. The results show that significant variations in metal sources existed in Bergslagen for the volcanogenic ores. Most ores (including the Falun Cu-Zn-Pb deposit) were formed from a major isotopic reservoir that occurs in the interior parts of Bergslagen. This source is defined as the Falun reservoir and is dominated by calcalkaline felsic volcanic rocks. A variable input from a more evolved source component (recycled pre-Svecofennian crustal components) is locally important in sedimentdominated areas, particularly the Stockholm archipelago. A third source, representing relatively primitive metabasalts, influenced the lead isotopic pattern of ores in westernmost Bergslagen. The composition of the Zinkgruvan (Åmmeberg) ore lead is distinctly different from that of the Falun reservoir, but forms, together with other sulphide deposits along the southern margin of Bergslagen, a pronounced linear trend in standard isotope diagrams. The linear trend is interpreted as a mixing line and shows that the lead in these ores were derived partly from evolved and partly from primitive sources. The evolved end member has an isotopic composition, which is comparable with the sediment-dominated sources in the interior parts of Bergslagen and in the Stockholm archipelago. The primitive end member is represented by tholeiitic volcanics, which are more abundant in the southern margin of Bergslagen than elsewhere in Bergslagen. A significant variation with respect to metal sources and depositional environments can thus be recognized for the Bergslagen ores and a renaissance for the genetic concepts Falun and Åmmeberg types is suggested.  相似文献   

15.
A mechanical decrepitation device coupled with a gas chromatograph has been used to characterize the molecular composition of gaseous and liquid hydrocarbons contained in minerals. Application of this technique allows the identification of low-molecular-weight n-alkanes and some aromatic hydrocarbons in sulfides and gangue minerals from epigenetic Variscan and post-Variscan lead–zinc deposits in the Rhenish Massif, Germany. Based on the analysis of 200 samples, Variscan and post-Variscan mineralization can be distinguished by the composition of associated hydrocarbons. Variscan sulfides and gangue minerals contain high abundancies of methane. In contrast, n-alkanes in the C2–C9 range and aromatic hydrocarbons (benzene, toluene) are dominant in post-Variscan mineralization. The absence of high-molecular-weight hydrocarbons in ore minerals suggests highly mature gas associated with hydrothermal activity, during which hydrothermal fluids caused an increase in thermal maturation of organic matter and the generation of low-molecular-weight hydrocarbons in the adjacent organic-rich rocks. The hydrocarbon compositions contained in fluid inclusions of Variscan and post-Variscan minerals are probably governed by the maturation level of the potential source rocks. In Variscan time tectonic brines (T > 175 °C) generated predominantly methane, whereas basement brines (T < 175 °C) expelled higher-molecular-weight hydrocarbons (wet gases, condensates, aromatic hydrocarbons) from adjacent rocks during the Mesozoic event. The specific role of hydrocarbons in sulfide precipitation via thermochemical sulfate reduction is indicated by geochemical characteristics of organic matter associated with the Plombières Pb–Zn deposit, in eastern Belgium. Intense alteration phenomena were observed in near-ore kerogens, compared with unaltered kerogens far from the ore body, as well as by a very high maturity (5.40% Ro), a systematic depletion in 12C towards the vein-type mineralization, high atomic S/C ratios (0.49), and by low atomic H/C ratios (0.29). The data suggest that hydrothermal solutions caused a drastic increase in the thermal maturation of organic matter within the adjacent wall rock. Increased thermal maturation resulted in increased δ13C-values of organic carbon due to the preferential release of 12C. The change in the organic matter to a H-depleted and S-enriched bulk composition in association with sulfide ores strongly suggests that thermochemical sulfate reduction was responsible for organic degradation. Thus, thermochemical sulfate reduction probably triggered base metal sulfide precipitation in Variscan and post-Variscan ore deposits of the Rhenish Massif. Finally, based on data from this study and previous investigations, new genetic models are presented for both Variscan and post-Variscan mineralization in the Rhenish Massif. Received: 15 September 1999 / Accepted: 2 December 1999  相似文献   

16.
The Chelopech deposit is one of the largest European gold deposits and is located 60 km east of Sofia, within the northern part of the Panagyurishte mineral district. It lies within the Banat–Srednegorie metallogenic belt, which extends from Romania through Serbia to Bulgaria. The magmatic rocks define a typical calc-alkaline suite. The magmatic rocks surrounding the Chelopech deposit have been affected by propylitic, quartz–sericite, and advanced argillic alteration, but the igneous textures have been preserved. Alteration processes have resulted in leaching of Na2O, CaO, P2O5, and Sr and enrichment in K2O and Rb. Trace element variation diagrams are typical of subduction-related volcanism, with negative anomalies in high field strength elements (HFSE) and light element, lithophile elements. HFSE and rare earth elements were relatively immobile during the hydrothermal alteration related to ore formation. Based on immobile element classification diagrams, the magmatic rocks are andesitic to dacitic in compositions. Single zircon grains, from three different magmatic rocks spanning the time of the Chelopech magmatism, were dated by high-precision U–Pb geochronology. Zircons of an altered andesitic body, which has been thrust over the deposit, yield a concordant 206Pb/238U age of 92.21 ± 0.21 Ma. This age is interpreted as the crystallization age and the maximum age for magmatism at Chelopech. Zircon analyses of a dacitic dome-like body, which crops out to the north of the Chelopech deposit, give a mean 206Pb/238U age of 91.95 ± 0.28 Ma. Zircons of the andesitic hypabyssal body hosting the high-sulfidation mineralization and overprinted by hydrothermal alteration give a concordant 206Pb/238U age of 91.45 ± 0.15 Ma. This age is interpreted as the intrusion age of the andesite and as the maximum age of the Chelopech epithermal high-sulfidation deposit. 176Hf/177Hf isotope ratios of zircons from the Chelopech magmatic rocks, together with published data on the Chelopech area and the about 92-Ma-old Elatsite porphyry–Cu deposit, suggest two different magma sources in the Chelopech–Elatsite magmatic area. Magmatic rocks associated with the Elatsite porphyry–Cu deposit and the dacitic dome-like body north of Chelopech are characterized by zircons with ɛHfT90 values of ∼5, which suggest an important input of mantle-derived magma. Some zircons display lower ɛHfT90 values, as low as −6, and correlate with increasing 206Pb/238U ages up to about 350 Ma, suggesting assimilation of basement rocks during magmatism. In contrast, zircon grains in andesitic rocks from Chelopech are characterized by homogeneous 176Hf/177Hf isotope ratios with ɛHfT90 values of ∼1 and suggest a homogeneous mixed crust–mantle magma source. We conclude that the Elatsite porphyry–Cu and the Chelopech high-sulfidation epithermal deposits were formed within a very short time span and could be partly contemporaneous. However, they are related to two distinct upper crustal magmatic reservoirs, and they cannot be considered as a genetically paired porphyry–Cu and high-sulfidation epithermal related to a single magmatic–hydrothermal system centered on the same intrusion.  相似文献   

17.
The recently discovered Hanshan gold deposit in northern Gansu Province, northwestern China, is hosted by a WNW-striking shear zone in Ordovician andesite and basalt. Mineralization consists of surface to near-surface oxidized ore (the yellow sandy gossan type) and three types of primary ore, i.e. early-stage quartz-sericite-pyrite ores in stockworks, early-stage disseminated ore, and the most important late-stage quartz ± calcite-sulfide veins. The ore system is characterized by variable degrees of potassic and silicic alteration. Late-stage gold-related fluid inclusions have homogenization temperatures between 170 to 310 °C, with a peak around 260 °C and low salinities. The ore fluids had high contents of CO2, CH4, and N2. Sulfur isotope measurements of −1.9 to +1.7 per mil for hydrothermal pyrites could be consistent with a hydrothermal fluid source from the mantle, but the oxygen and carbon isotope data from calcite and quartz suggest mixing between mantle and crustal fluid sources. K-Ar ages for hydrothermal sericite from ore zones are 213.9 ± 3.1 and 224.4 ± 3.2 Ma. Due to the arid Cenozoic climate, a yellow gold-bearing gossan developed, which consists of jarosite, gypsum, and relict quartz. It could be a widespread and useful prospecting guide for gold in northwestern China. Received: 1 February 1999 / Accepted: 1 August 1999  相似文献   

18.
 Single zircon U–Pb dating combined with 207Pb/206Pb ages obtained by the evaporation method constrains the emplacement of tonalitic, trondhjemitic, and granodioritic orthogneisses of the Moldanubian zone in the Black Forest between 500 and 510 Ma. Two detrital zircon populations of 1.9 and 1.6 Ga indicate Early-Middle Proterozoic material in the former setting of the basement. The initial eNd values range from –0.1 to –3.4 and mean crustal residence ages of 1.0–1.4 Ga are consistent with involvement of Early-Middle Proterozoic crust, and a subordinate juvenile component probably originating from subduction-related melting of the mantle. The orthogneisses have fractionated REE patterns and slightly higher K2O/Na2O ratios than typical low-K tonalite–trondhjemite–granite suites. The chemical data are interpreted as evidence for melting of amphibolite and contributions from evolved crust. The emplacement of the orthogneisses was superceded by a high-temperature metamorphic event at ∼480 Ma which we interpret as a result of lithospheric thinning in a marginal basin behind a Cambrian magmatic arc. Received: 29 March 1999 / Accepted: 25 August 1999  相似文献   

19.
The Rammelsberg polymetallic massive sulphide deposit was the basis of mining activity for nearly 1000 y before finally closing in 1988. The deposit is hosted by Middle Devonian pelitic sediments in the Rhenohercynian terrane of the Variscan Orogen. The deposit consists of two main orebodies that have been intensely deformed. Deformation obscures the original depositional relationships, but the regional setting as well as the geochemistry and mineralogy of the mineralisation display many characteristics of the SHMS (sediment-hosted massive sulphide) class of ore deposits. Rammelsberg is briefly compared to the other massive sulphide deposits in the European Variscan, including Meggen and those deposits in the Iberian Pyrite Belt. Received: 28 September 1998 / Accepted: 5 January 1999  相似文献   

20.
Summary Rare Earth Element (REE) data of 34 samples of magmatic rocks from the Lofoten Islands in Norway lend support to the derivation of anorthosites, ferrodiorites and jotunites by fractionation and cumulus processes from typical basaltic magma. Both REE concentration and Eu anomalies (expressed as Eu/Eu*) form continuous linear trends from anorthosite towards gabbro, ferrodiorite and jotunite in discrimination diagrams against molar CaO/Al2O3 ratios indicating the predominant accumulation of plagioclase. Eu/Eu* decreases from about 4 in the cumulates (anorthosites) to around 1 in the fine-grained gabbroic dikes and to below 1 in some ferrodiorites and the jotunite. The various types of ferrodiorites and the jotunite are regarded as residual liquids, in some cases with variable amounts of cumulus plagioclase. The whole fractionation series from gabbro towards anorthosites and ferrodiorites can be observed in a single intrusion. With increasing fractionation, the REE patterns generally change from flat, slightly LREE-enriched or LREE-depleted to steep and strongly LREE-enriched. These changes and the REE abundances are mainly controlled by the abundance of apatite. Temporally and spatially related mangerites and charnockites form a trend from low-SiO2 mangerites with Eu/Eu* > 1 to intermediate-SiO2 acidic mangerites with Eu/Eu* ≈ 1 and charnockites with Eu/Eu* < 1. Accordingly, the low-SiO2 mangerites are interpreted as alkali feldspar-rich cumulates and the charnockites as residual liquids derived from the acidic mangerites. The mangerites with Eu/Eu* around 1 have patterns similar to those of some highly evolved ferrodiorites possibly indicating a genetic link. Received December 12, 1999; revised version accepted November 15, 2000  相似文献   

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