首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 93 毫秒
1.
New data are reported on the localization and genesis of PGE mineralization at the South Sopcha deposit situated in the southern framework of the Monchegorsk pluton. Disseminated PGE-Cu-Ni mineralization, the thickness of which in particular boreholes exceeds 100 m, is hosted in the zone of alternating peridotite, pyroxenite, norite, and gabbronorite. The PGE grade does not exceed 1?C2 gpt with Pd/Pt = 3?C4 at Ni and Cu contents from 0.2 to 1.5 wt %. The PGE contents up to 4?C6 gpt and Pd/Pt = 4?C8 are noted at local sites of hydrothermally altered rocks. Another type of PGE mineralization is established in the outcrops of the southeastern marginal group of the massif. Pyroxenite, norite, and gabbronorite fragments are incorporated here in the gabbroic matrix, making up a complex zone of magmatic breccia complicated by mylonites and late injections. Elevated PGE contents (1.0?C6.5 gpt) are detected in all types of rocks in the zone of brecciation, mainly in the matrix. Platinum-group minerals (PGM) occur in association with magmatic and late sulfides, amphibole, mica, and chlorite. PGM vary in composition depending on the petrographic features of rocks. In rocks of the layered series and in pegmatoid pyroxenite PGM are extremely diverse comprising PGE compounds with As, Sb, Bi, Te, Se, and S. In the brecciated rocks of the marginal group, Pd bismuthotellurides (mainly merenskyite), sperrylite, hollingworthite, and Pd- and Rh-bearing cobaltite and gersdorffite are predominant. The PGE mineralization in rocks of the layered series and pegmatoid pyroxenite was formed from the magmatic melt enriched in volatiles and with subsequent transformation of PGE assemblages under the influence of hydrothermal fluids at a lower temperature. In gabbroic rocks of the marginal group, PGM are associated with the latest sulfides (chalcopyrite, bornite, chalcocite), forming separate grains and thin veinlets in hydrothermally altered rocks. The gabbroic melt affected incompletely crystallized rocks of the layered series by formation of contact-type PGE mineralization, deposition and redeposition of ore matter.  相似文献   

2.
The geology of the basal-structural Loypishnyun low-sulfide Pt–Pd deposit is characterized, including its mineral composition and the peculiarities of its PGE and chalcophile-element distribution in ore. The deposit is situated in the northeastern part of the Monchetundra basic massif and is localized in its lower norite–orthopyroxenite zone, intensely injected with late gabbroic rocks. Two ore zones are distinguished within the deposit. Ore zone 1 has been traced by drilling for about 1.5 km at a thickness from 10–15 to 120 m and incorporates from two to nine separate lenticular–sheetlike orebodies 0.5–25 m in thickness. Ore zone 2 has been traced for 550 m and is represented by one orebody 5–35 m thick. The internal structure of the orebodies is characterized by alternation of low-grade (Pt + Pd = 0.5–0.9 gpt), ordinary (Pt + Pd = 1.0–1.9 gpt), and high-grade (Pt + Pd > 2 gpt) interlayers of various thickness. The ores are spatially and genetically related to sulfide mineralization (pentlandite–chalcopyrite–pyrrhotite) in an amount of 1–5 vol %. The PGE distribution in ores normalized to primitive mantle is characterized by fractionation of easily fusible platinoids with a positive Pd anomaly. The spectra of chalcophile elements normalized to primitive mantle are notable for elevated Te, Bi, As, and Se contents with respect to Sn, Hg, and Pb, which reflects the significant contribution of Te, Bi, and As in the formation of platinum group minerals (PGM), whereas Se, which is devoid of proper mineral phases, most likely is an admixture in the composition of sulfides. The S/Se value in ore of the Loypishnyun deposit varies from 31 to 814. The platinum group elements (PGE) in ore are represented by 45 noble metal minerals. Ore zone 1 is characterized by lateral mineral zoning, which is expressed as replacement of a bismuthotelluride–sulfide PGM assemblage by an assemblage of copper–PGE compounds and alloys. In ore zone 2, a mineral assemblage of tellurides, copper–PGE compounds and alloys predominates, with native gold, silver, and palladium, as well as sulfides and bismuthotellurides, playing a subordinate role. The formation of PGM ore proceeded under variable sulfur fugacity conditions, beginning with the late magmatic stage at temperatures of 900–700°C and ending with hydrothermal transformation at a temperature of <500°C.  相似文献   

3.
The Kaalamo massif is located in the Northern Ladoga region, Karelia, on the extension of the Kotalahti Belt of Ni-bearing ultramafic intrusions in Finland. The massif, 1.89 Ga in age, is differentiated from pyroxenite to diorite. Nickel–copper sulfide mineralization with platinoids is related to the pyroxenite phase. The ore consists of two mineral types: (i) pentlandite–chalcopyrite–pyrrhotite and (ii) chalcopyrite, both enriched in PGE. Pd and Pt bismuthotellurides, as well as Pd and Pt tellurobismuthides, are represented by the following mineral species: kotulskite, sobolevskite, merenskyite, michenerite, moncheite, keithconnite, telluropalladinite; Pt and Pd sulfides comprise vysotskite, cooperite, braggite, palladium pentlandite, and some other rare phases. High-palladium minerals are contained in pentlandite–chalcopyrite–pyrrhotite ore. Native gold intergrown with kotulskite commonly contains microinclusions (1–3 μm) of Pd stannides: paolovite and atokite. Ore with 20–60% copper sulfides (0.2–6.0% Cu) contains 5.1–6.6 gpt PGE and up to 0.13–2.3 gpt Au. Pd minerals, arsenides and sulfoarsenides of Pt, Rh, Ir, Os, and Ru are identified as well. These are sperrylite, ruthenium platarsite, hollingworthite, and irarsite; silvery gold and paolovite have also been noted. All these minerals have been revealed in the massif for the first time. The paper also presents data on the compositions of 25 PGE minerals (PGM) from Kaalamo ores.  相似文献   

4.
The Early Paleoproterozoic Monchegorsk Complex comprises two independent large layered mafic-ultramafic intrusions: the Monchegorsk pluton and the Main Range massif formed about 2.50 and 2.46 Ga ago, respectively. They are composed of similar cumulates, though they differ somewhat in the isotopic parameters of rocks, cumulate stratigraphy and derived from siliceous high-Mg series melts that arose in the same large long-living volcanic center. The economic syngenetic Ni-Cu-PGE sulfide mineralization related to the earlier Monchegorsk pluton is represented by two types of ores. The first type, pertaining to fractionation of the primary melt, is opposite to the reef formed due to injection of a special ore-bearing melt into the solidifying intrusive chamber. The primary magmatic mineralization is largely composed of Ni-Fe-Cu sulfides and Pd-Pt sulfides, bismuthides, and tellurides. Only small PGE and probably chromite occurrences are related to the Main Range massif. In the Mid-Paleoproterozoic (2.0-1.9 Ga), the complex was transformed into a collage of tectonic blocks confined to the regional fault zone. The Monchegorsk pluton was retained better, and only rocks of its southern framework were involved into tectonic and metamorphic reworking with the formation of economic metamorphic low-sulfide PGE mineralization with widespread Pd and Pt telluro-bismuthides, arsenides, stannides, antimonides, and selenides. The ore formation was accompanied by PGE redistribution and segregation of lenticular orebodies with diffuse contours. Thus, the Monchegorsk ore cluster is characterized by juxtaposition of unaltered primary magmatic deposits and those formed as a result of their metamorphism and distinguished from the former by structure and composition. The comparative study of these deposits opens up new possibilities for comprehending ore-forming processes in the same situations.  相似文献   

5.
The geology and mineralogy of host metamorphic rocks, the mineralogy of sulfide ores, and the distribution of PGE mineralization were studied in detail for the Kvinum-1 and Kvinum-2 copper-nickel occurrences of the Kvinum ore field, which are the most promising targets for the copper-nickel-PGE mineralization of the Sredinny Range of Kamchatka. It was established that stringer-disseminated and massive copper-nickel ores are localized in amphibole peridotites, cortlandites, and form ore bodies varying from tens of centimeters to 5–20 m thick among the layered cortlandite-gabbroid massifs. The massive sulfide ores were found only at the bottom of cortlandite bodies and upsection grade into stringer-disseminated and disseminated ores. Pyrrhotite, chalcopyrite, and pentlandite are the major ore minerals with a sharply subordinate amount of pyrite, sphalerite, galena, arsenopyrite, and löllingite. Besides pentlandite, the Ni-bearing minerals include sulforasenides (gersdorffite), arsenides (nickeline), and tellurides (melonite) of nickel. It was found that PGE mineralization represented by antimonides (sudburyite) and tellurobismuthides (michenerite) of Pd with sharply subordinate platinum arsenide (sperrylite) is confined to the apical parts of massive sulfide zones and the transition zone to the stringer-disseminated ores. Ore intervals enriched in arsenides and tellurides of Ni, Pd, and Bi contain high-purity gold. In the central parts of the orebodies, the contents of PGE and native gold are insignificant. It is suggested that the contents of major sulfide minerals and the productivity of PGE mineralization in the cortlandites are defined by combined differentiation and sulfurization of ultramafic derivatives under the effect of fluids, which are accumulated at the crystallization front and cause layering of parental magmas with different sulfur contents. The fluid-assisted layering of mafic-ultramafic massifs resulted in the contrasting distribution of PGM in response to uneven distribution of sulfur (as well as As, Te, and Bi) during liquid immiscibility. The productivity of PGE mineralization significantly increases with increasing contents of S, As, Te, and Bi (elements to which Pt and, especially, Pd have high affinity) in fluids.  相似文献   

6.
Mineralization composed dominantly of primary troilite, maucherite, pentlandite, and chalcopyrite, and secondary valleriite occurs in serpentinized transition zone rocks of the Limasol Forest segment of the Troodos ophiolite complex, Cyprus. Whole-rock and electron microprobe analyses of this mineralization gives ranges of Cu/(Cu+Ni)=0.16 to 0.47, Pt/(Pt+Pd)=0.66 to 0.51, Ni/Co=6.33 to 13.4, and chondrite normalized plots with low concentrations of Rh, Pt, and Pd, but relatively high Au. Estimated distribution coefficients of nickel and iron between olivine and ore range from 0.5 to 7.4. Most of these data are unlike values from magmatic sulfide deposits and indicate either a complete alteration of a preexisting magmatic sulfide concentration or, more likely, a nonmagmatic origin for this mineralization.  相似文献   

7.
Stratigraphic offsets in the peak concentrations of platinum-group elements (PGE) and base-metal sulfides in the main sulfide zone of the Great Dyke and the precious metals zone of the Sonju Lake Intrusion have, in part, been attributed to the interaction between magmatic PGE-bearing base-metal sulfide assemblages and hydrothermal fluids. In this paper, we provide mineralogical and textural evidence that indicates alteration of base-metal sulfides and mobilization of metals and S during hydrothermal alteration in both mineralized intrusions. Stable isotopic data suggest that the fluids involved in the alteration were of magmatic origin in the Great Dyke but that a meteoric water component was involved in the alteration of the Sonju Lake Intrusion. The strong spatial association of platinum-group minerals, principally Pt and Pd sulfides, arsenides, and tellurides, with base-metal sulfide assemblages in the main sulfide zone of the Great Dyke is consistent with residual enrichment of Pt and Pd during hydrothermal alteration. However, such an interpretation is more tenuous for the precious metals zone of the Sonju Lake Intrusion where important Pt and Pd arsenides and antimonides occur as inclusions within individual plagioclase crystals and within alteration assemblages that are free of base-metal sulfides. Our observations suggest that Pt and Pd tellurides, antimonides, and arsenides may form during both magmatic crystallization and subsolidus hydrothermal alteration. Experimental studies of magmatic crystallization and hydrothermal transport/deposition in systems involving arsenides, tellurides, antimonides, and base metal sulfides are needed to better understand the relative importance of magmatic and hydrothermal processes in controlling the distribution of PGE in mineralized layered intrusions of this type.  相似文献   

8.
The Pt-Pd and Au-Ag mineralization hosted in both wehrlite without visible links to sulfide mineralization (dispersed assemblage of the Tartai massif) and disseminated Cu-Ni sulfide ore (ore assemblage of the Ognit massif) was found in dunite-wehrlite massifs localized in the fold framework of the Siberian Craton. The Pt minerals in both assemblages comprise sperrylite (PtAs2) and secondary Pt-Fe-Ni alloys in the Ognit massif and Pt-Fe-Cu and Pt-Cu alloys in the Tartai massif. The Pd minerals are widespread in the ore assemblages as compounds with Te, Sb, and Bi, whereas in the dispersed assemblage Pd is concentrated primarily in Pd-Cu-Sb compounds. Both assemblages are characterized by similar substitution of sperrylite with orcelite (Ni5 ? xAs2) and then with secondary Pt-Fe-Ni or Pt-Fe-Cu and Pt-Cu alloys; the occurrence of Au-Ag alloys with prevalence of Ag over Au; and replacement of them with auricupride (Cu3Au) at the late stage. Sperrylite in both assemblages contains Ir impurities, while the Pd minerals contain Cu and Ni admixtures, which are typical of mineral assemblages related to the ultramafic intrusions with nickel specialization. PGM were formed under a low sulfur fugacity and high As, Bi, and Sb activities. The postmagmatic fluids affected the primary mineral assemblages under reductive conditions, and this effect resulted in replacement of sperrylite with Ni arsenide (orcelite) and Pt-Fe-Ni and Pt-Fe-Cu alloys; Ni and Cu sulfides were replaced with awaruite and native copper.  相似文献   

9.
The Northern Ultramafic Centre (NUC) of the Lac des Iles Complex, Northwest Ontario hosts several platinum group element (PGE) occurrences, including the Sutcliffe Zone, which consists of four subparallel, stratiform PGE-enriched intervals exposed within the cyclically layered eastern flank of the NUC. Field relationships, mineral paragenesis and lithogeochemistry allowed for the identification of 14 cyclic cumulate sequences of two distinct types – Cyclic unit type A (CUA) and Cyclic unit type B (CUB). CUA-type and CUB-type units are interpreted to have formed from a Si-enriched and Si-poor parent magmas, respectively. PGE-enriched intervals occur in four of the CUA-type cyclic units (CUA-5, -6, -8 and -11). PGE enriched intervals are commonly associated with websterite, olivine websterite and gabbronorite containing primary disseminated sulfide (0.2–2 vol%) which are dominated by pyrrhotite, chalcopyrite, and pentlandite with minor cubanite, and troilite. In hydrothermally altered rocks enriched in PGE, primary sulfides are locally partially replaced by secondary chalcopyrite, sphalerite, heazlewoodite, and chalcocite. Palladium occurs either in solid solution with primary pentlandite or is associated with platinum group minerals (PGM) such as Pd-plumbide, Pd-telluride, and Pt-bismuthotelluride. PGMs commonly occur within primary sulfides, at contacts between primary sulfide–silicate minerals, or in association with secondary serpentine and actinolite. Gold and silver typically occur as electrum that exhibits similar textural characteristics and mineralogical associations as the PGMs.Two different chemostratigraphic patterns of PGE, Cu and S enrichment can be recognized among the mineralized CUA cycles: The first (top-loaded) occurs near the top of CUA cycles (CUA-6, -8 and -11) in websterite and/or gabbronorite, just below the levels at which CUB magmas were emplaced. The second (middle-loaded), occurs midway through the lower cycle (CUA-5) in the olivine websterite, which is overlain by CUA-6. Within the four mineralized intervals, PGE tenors average 643 ppm Pd + Pt (in 100% sulfide), Pd/Pt and Pd/Ir ratios range from 0.9 to 3.5 and 35 to 537, respectively, and S/Se ratios range between 500 and 6000. The highest PGE tenors (4377 ppm Pd + Pt) are found in the lowermost interval in serpentinized olivine websterite and have an average Pd/Pt ratio of 3.5 and a S/Se ratio of approximately 2000.It is proposed that orthomagmatic processes of fractional crystallization and dynamic magma recharge were the dominant mineralization processes triggering sulfide-saturation and PGE concentration at the Sutcliffe Zone. Textural relationships between PGM, sulfide minerals, and primary and secondary hydrous silicates suggest that late magmatic to postcumulus hydrothermal fluid infiltration occurred locally during and after sulfide mineralization of the PGE-enriched intervals. However, these fluids had a minimal effect on the distribution of PGE in the Sutcliffe Zone. The Sutcliffe Zone shares many similarities with classic stratiform PGE deposits in terms of Pd/Pt ratio, high PGE tenors, low abundance of sulfide, and PGM assemblages. However, it is distinguished from most stratiform PGE deposits by its tectonic environment and lithostratigraphic position and by the intimate spatial association of the two parental magmas that are interpreted to have been responsible for the observed chemostratigraphy and PGE enrichment.  相似文献   

10.
喀拉通克铜镍矿床位于准噶尔板块北缘,矿区主要矿体赋存于Y1-Y3号岩体中。矿石构造类型为致密块状和浸染状两大类,其中前者与后者呈贯入接触,不同浸染状类型之间为过渡关系。岩石和矿石的PGE总量偏低,且以PPGE为主,IPGE含量较低。整体上岩石中的PGE含量显示随基性程度降低而变小。矿石中的PGE含量随硫化物含量增加增大,显示PGE主要分布于硫化物熔离形成的物相中。100%硫化物计算后,矿石PGE含量平均仅为573×10-9。各岩体中浸染状矿石PGE组成并无明显差异;岩石和矿石具有相似的PGE分配模式,均属于Pt-Pd配分型。岩石Ni/Cu-Pd/Ir关系以及岩石地球化学资料显示,形成喀拉通克岩体的初始岩浆为MgO含量较高的玄武质岩浆,属于PGE不亏损的岩浆。基于PGE不亏损的大陆拉斑玄武岩初始岩浆推算,喀拉通克矿床母岩浆明显亏损PGE,而深部硫化物熔离可能是导致母岩浆PGE亏损的主要原因。岩石和矿石Pd/Pt比值总体特征,岩石Cr与Ni、Ir、Ru和Rh相关性,以及硫同位素和岩石学资料分析表明,初始岩浆在地壳深部发生的橄榄石、铬铁矿等矿物的分离结晶作用,可能是促使硫过饱和与深部熔离的主要因素。IPGE与PPGE分异特征及其相关分析,结合矿床宏观地质特征,推断该矿床浸染状矿的成矿作用经历了初始岩浆（PGE不亏损）→橄榄石等矿物分离结晶→硫化物深部熔离→成矿母岩浆（PGE亏损）→上侵并结晶分异的成矿过程。块状矿则可能是这一过程中PGE亏损的成矿母岩浆相对滞后熔离形成的硫化物熔体贯入的结果。  相似文献   

11.
Summary An unusually thick sulfur-poor mineralized zone enriched in platinum-group elements (PGE) is described in the Hanumalapur Complex, Shimoga District, Karnataka State, India. This promising occurrence was discovered in the early 1990s and the best samples at the time of writing have yielded Pt+Pd concentrations in excess of six ppm. The western part of the area concerned belongs to the late Archaean Dharwar Super Group (3000–2500 Ma), while the eastern part is occupied predominantly by a granite-gneiss terrain ∼3000 Ma in age. Ten mafic-ultramafic complexes which host interesting vanadium-bearing titanomagnetite occurrences are encountered in the western part, one of which is the Hanumalapur Complex. The PGE mineralized zone in this complex may be divided into four mineralogically distinctive types, which are, in descending order of PGE content: 1) a silicate-hosted Pd type, 2) a silicate-hosted Pt type, 3) a base-metal sulfide-hosted Pd type, and 4) an oxide-hosted PGE type. The genesis of the mineralization is somewhat unclear at this point of investigation, especially because of complete re-crystallization, but the evidence gathered so far suggests something different than a traditional orthomagmatic model requiring magma mixing processes and resulting in sulfide immiscibility. This is backed-up by the general lack of base metal sulfides in favor of chromite, although pure chlorite-amphibole and chlorite-albite-epidote-amphibole rocks may contain significant PGE concentrations regardless of the amount of chromite. The PGM textures show little evidence of hydrothermal alteration and remobilization, but the PGE mineralogy itself displays some characteristics of fluid action, as it seems that there are some OH-bearing Pt and Pd minerals present. The first author was Deceased Author’s address: R. J. Kaukonen, Department of Geosciences, University of Oulu, Oulu, P.O. Box 3000, FIN-90014 Finland  相似文献   

12.
The Kalatongke (also spelt as Karatungk) Ni–Cu–(platinum-group element, PGE) sulfide deposit, containing 33 Mt sulfide ore with a grade of 0.8 wt.% Ni and 1.3 wt.% Cu, is located in the Eastern Junggar terrane, Northern Xinjiang, NW China. The largest sulfide ore body, which occupies more than 50 vol.% of the intrusion Y1, is dominantly comprised of disseminated sulfide with a massive sulfide inner zone. Economic disseminated sulfides also occur at the base of the intrusions Y2 and Y3. The main host rock types are norite in the lower part and diorite in the upper part of each intrusion. Enrichment in large ion lithophile elements and depletion in heavy rare earth elements relative to mid-ocean ridge basalt indicate that the mafic intrusions were produced from magmas derived from a metasomatized garnet lherzolite mantle. The average grades of the disseminated ores are 0.6 wt.% Ni and 1.1 wt.% Cu, whereas those of the massive ores are 2 wt.% Ni and 8 wt.% Cu. The PGE contents of the disseminated ores (14–69 ppb Pt and 78–162 ppb Pd) are lower than those of the massive ores (120–505 ppb Pt and 30–827 ppb Pd). However, on the basis of 100% sulfide, PGE contents of the massive sulfides are lower than those of the disseminated sulfides. Very high Cu/Pd ratios (>4.5 × 104) indicate that the Kalatongke sulfides segregated from PGE-depleted magma produced by prior sulfide saturation and separation. A negative correlation between the Cu/Pd ratio and the Pd content in 100% sulfide indicates that the PGE content of the sulfide is controlled by both the PGE concentrations in the parental silicate magma and the ratio of the amount of silicate to sulfide magma. The negative correlations between Ir and Pd indicate that the massive sulfides experienced fractionation.  相似文献   

13.
After the discovery of the Aguablanca ore deposit (the unique Ni–Cu mine operating in SW Europe), a number of mafic‐ultramafic intrusions bearing Ni–Cu magmatic sulfides have been found in the Ossa–Morena Zone of the Iberian Massif (SW Iberian Peninsula). The Tejadillas prospect is one of these intrusions, situated close to the border between the Ossa–Morena Zone and the South Portuguese Zone of the Iberian Massif. This prospect contains an average grade of 0.16 wt % Ni and 0.08 wt % Cu with peaks of 1.2 wt % Ni and 0.2 wt % Cu. It forms part of the Cortegana Igneous Complex, a group of small mafic‐ultramafic igneous bodies located 65 km west of the Aguablanca deposit. In spite of good initial results, exploration work has revealed that sulfide mineralization is much less abundant than in Aguablanca. A comparative study using whole‐rock geochemical data between Aguablanca and Tejadillas shows that the Tejadillas igneous rocks present a lower degree of crustal contamination than those of Aguablanca. The low crustal contamination of the Tejadillas magmas inhibited the assimilation of significant amounts of crustal sulfur to the silicate magmas, resulting in the sparse formation of sulfides. In addition, Tejadillas sulfides are strongly depleted in PGE, with total PGE contents ranging from 14 to 81 ppb, the sum of Pd and Pt, since Os, Ir, Ru and Rh are usually below or close to the detection limit (2 ppb). High Cu/Pd ratios (9700–146,000) and depleted mantle‐normalized PGE patterns suggest that the Tejadillas sulfides formed from PGE‐depleted silicate magmas. Modeling has led us to establish that these sulfides segregated under R‐factors between 1000 and 10,000 from a silicate melt that previously experienced 0.015% of sulfide extraction. All these results highlight the importance of contamination processes with S‐rich crustal rocks and multiple episodes of sulfide segregations in the genesis of high‐tenor Ni–Cu–PGE ore deposits in mafic‐ultramafic intrusions of the region.  相似文献   

14.
PGE-rich disseminated zones with discrete platinum-group minerals (Pd, Pt and Rh mineral phases) have been discovered in three thick (80–130 m), differentiated (peridotite-gabbro) mafic-ultramafic flows of the Archean Abitibi greenstone belt, Ontario. Three mineralization zones (whole-rock ∑PGE + Au = up to 1000 ppb) occur along four stratigraphic cross sections through a 2 km strike-length of the Boston Creek Flow ferropicritic basalt. Their occurrence most strikingly correlates with lenticular-podiform concentrations of disseminated chalcopyrite (1 %) and clinopyroxene + interstitial magnetite-ilmenite intergrowths (15–20% oxide), high concentrations of related metals (3000 ppm Cu, 3000 ppm S, 1200 ppb Ag, and 1000 ppm V), strong PGE depletion in adjacent rocks and along strike, and lithological and textural complexity in the margins of the central gabbro-diorite layer. The mineralization zone (whole-rock Ir + Pt + Pd + Au = 110 ppb) within Theo's Flow tholeiitic basalt is somewhat similar in occurrence, style, and composition to those within the Boston Creek Flow. In contrast, the mineralization zone (whole-rock Ir + Pt + Pd + Au = 340 ppb) in Fred's Flow komatiitic basalt most strikingly correlates with vesicle-filling intergrowths of pyrrhotite + pentlandite ± chalcopyrite (2 modal %) and high whole-rock concentrations of Ni (2500 ppm), Cu (700 ppm), and S (1.1%) in the upper chilled margin of the flow.Although apparently uneconomic, these flow-hosted PGE mineralization zones are of interest in exploration, because they are more similar in stratigraphie setting, style, and composition to PGE-rich disseminated Fe-Cu sulfide mineralization zones within thick differentiated intrusions than to mineralization zones in other Archean volcanic rocks. The characteristics of the mineralization zones and their host rocks, especially high degrees of PGE enrichment, vertical and horizontal patterns of PGE depletion, and accumulation of clinopyroxene + magnetite-ilmenite intergrowths, indicate a critical genetic role for variations in the regime of melt flowage. The mineralization zones in the Boston Creek and Theo's Flows are interpreted to have formed by simultaneous in situ formation of PGE-rich Fe-Cu sulfide and Fe-Ti oxide from flowing silicate liquid in the margins of internal lava channels. The mineralization zone in Fred's Flow is interpreted to have formed by ponding and coalescence of PGE-enriched sulfurous vapor bubbles in the upper chilled margin during olivine accumulation on the base of a dynamic lava channel. The relative abundance of PGE mineralization zones and high degree of PGE enrichment in the Boston Creek Flow suggest that the most favorable exploration targets are rocks crystallized from late-stage, highly fractionated derivative liquids in large differentiated terropicritic units.  相似文献   

15.
The Grasvally Norite–Pyroxenite–Anorthosite (GNPA) member within the northern limb of the Bushveld Complex is a mineralized, layered package of mafic cumulates developed to the south of the town of Mokopane, at a similar stratigraphic position to the Platreef. The concentration of platinum-group elements (PGE) in base metal sulfides (BMS) has been determined by laser ablation inductively coupled plasma–mass spectrometry. These data, coupled with whole-rock PGE concentrations and a detailed account of the platinum-group mineralogy (PGM), provide an insight into the distribution of PGE and chalcophile elements within the GNPA member, during both primary magmatic and secondary hydrothermal alteration processes. Within the most unaltered sulfides (containing pyrrhotite, pentlandite, and chalcopyrite only), the majority of IPGE, Rh, and some Pd occur in solid solution within pyrrhotite and pentlandite, with an associated Pt–As and Pd–Bi–Te dominated PGM assemblage. These observations in conjunction with the presence of good correlations between all bulk PGE and base metals throughout the GNPA member indicate the presence and subsequent fractionation of a single PGE-rich sulfide liquid, which has not been significantly altered. In places, the primary sulfides have been replaced to varying degrees by a low-temperature assemblage of pyrite, millerite, and chalcopyrite. These sulfides are associated with a PGM assemblage characterized by the presence of Pd antimonides and Pd arsenides, which are indicative of hydrothermal assemblages. The presence of appreciable quantities of IPGE, Pd and Rh within pyrite, and, to a lesser, extent millerite suggests these phases directly inherited PGE contents from the pyrrhotite and pentlandite that they replaced. The replacement of both the sulfides and PGM occurred in situ, thus preserving the originally strong spatial association between PGM and BMS, but altering the mineralogy. Precious metal geochemistry indicates that fluid redistribution of PGE is minimal with only Pd, Au, and Cu being partially remobilized and decoupled from BMS. This is also indicated by the lower concentrations of Pd evident in both pyrite and millerite compared with the pentlandite being replaced. The observations that the GNPA member was mineralized prior to intrusion of the Main Zone and that there was no local footwall control over the development of sulfide mineralization are inconsistent with genetic models involving the in situ development of a sulfide liquid through either depletion of an overlying magma column or in situ contamination of crustal S. We therefore believe that our observations are more compatible with a multistage emplacement model, where preformed PGE-rich sulfides were emplaced into the GNPA member. Such a model explains the development and distribution of a single sulfide liquid throughout the entire 400–800 m thick succession. It is therefore envisaged that the GNPA member formed in a similar manner to its nearest analogue the Platreef. Notable differences however in PGE tenors indicate that the ore-forming process may have differed slightly within the staging chambers that supplied the Platreef and GNPA member.  相似文献   

16.
The Jinchuan deposit, NW China, is one of the world’s most important Ni-Cu-(PGE) sulfide deposits related to a magma conduit system and is hosted in an ultramafic intrusion. The intrusion is composed of lherzolite and dunite with the two largest sulfide ore bodies (named as ore body 1 and 2) in its middle portion. The sulfide ores may be disseminated, net-textured, or massive. The disseminated and net-textured sulfide ores are characterized by variable but generally low PGE concentrations: 10-3200 ppb Pt, 240-9800 ppb Pd, 17-800 ppb Ir, 25-1500 ppb Ru, and 15-400 ppb Rh in 100% sulfides. The massive sulfide ores are extremely low in Pt (<30 ppb) on a 100% sulfides and have very high Cu/Pd ratios, ranging from 104 to 4.5 × 105. The low PGE contents suggest that the sulfide ores formed from the silicate magmas that had already experienced prior-sulfide separation.Our calculations indicate that if the first stage basaltic magmas had contained 6.3 ppb Pt, 6.2 ppb Pd, and 0.1 ppb Ir, 0.008% sulfide removal would result in PGE-depletion in the residual magma with 0.57 ppb Pt, 0.25 ppb Pd, and 0.009 ppb Ir. The Jinchuan sulfides were formed by a second stage of sulfide segregation from a PGE-depleted magma under silicate/sulfide liquid ratios (R-factor) ranging from 103 to 104 in a deep-seated staging chamber. The massive sulfide ores and some of the net-textured sulfide ores exhibit strong negative Pt-anomalies that cannot be explained by sulfide segregation under variable R-factors. Instead, the sulfide melts that formed the massive ores were segregated from magmas experienced prior fractionation of Pt-Fe alloy. Alternatively, the Pt may have been selectively leached by hydrothermal fluids during remobilization of the sulfide melts that produced the massive sulfides, which occur in cross-cutting veins. We propose that the Jinchuan intrusion and ore bodies were formed by injections of sulfide-free and sulfide-bearing olivine mushes from a deep-seated staging chamber.  相似文献   

17.
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   

18.
The Binchuan area of Yunnan is located in the western part of the Emeishan large igneous province in the western margin of the Yangtze Block.In the present study,the Wuguiqing profile in thickness of about 1440 m is mainly composed of high-Ti basalts,with minor picrites in the lower part and andesites,trachytes,and rhyolites in the upper part.The picrites have relatively higher platinum-group element（PGE） contents（ΣPGE=16.3-28.2 ppb）,with high Cu/Zr and Pd/Zr ratios,and low S contents（5.03-16.9 ppm）,indicating the parental magma is S-unsaturated and generated by high degree of partial melting of the Emeishan large igneous province（ELIP） mantle source.The slightly high Cu/Pd ratios（11 000-24 000） relative to that of the primitive mantle suggest that 0.007%sulfides have been retained in the mantle source.The PGE contents of the high-Ti basalts exhibit a wider range（ΣPGE=0.517-30.8 ppb）.The samples in the middle and upper parts are depleted in PGE and haveεNd（260 Ma） ratios ranging from -2.8 to -2.2,suggesting that crustal contamination of the parental magma during ascent triggered sulfur saturation and segregation of about 0.446%-0.554% sulfides,and the sulfide segregation process may also provide the ore-forming material for the magmatic Cu-Ni-PGE sulfide deposits close to the studied basalts.The samples in this area show Pt-Pd type primitive mantle-normalized PGE patterns,and the Pd/Ir ratios are higher than that of the primitive mantle（Pd/Ir=1）,indicating that the obvious differentiation between Ir-group platinum-group elements（IPGE） and Pd-group platinum-group elements（PPGE） are mainly controlled by olivine or chromites fractionation during magma evolution.The Pd/Pt ratios of most samples are higher than the average ratio of mantle（Pd/Pt=0.55）,showing that the differentiation happened between Pt and Pd.The differentiation in picrites may be relevant to Pt hosted in discrete refractory Pt-alloy phase in the mantle;whereas the differentiation in the high-Ti basalts is probably associated with the fractionation of Fe-Pt alloys,coprecipitating with Ir-Ru-Os alloys.Some high-Ti basalt samples exhibit negative Ru anomalies,possibly due to removal of laurite collected by the early crystallized chromites.  相似文献   

19.
Ongoing underground exploration in the giant Jinchuan Ni-Cu sulfide deposit in western China is beginning to emphasize the potential for Cu-, Pt-, and Pd-rich sulfide ores that may have formed by sulfide liquid fractionation. The success of such an effort relies on whether or not fractional crystallization of sulfide occurred in the Jinchuan system. In this paper, we used available PGE data to evaluate such a process. We found that about two thirds of the 126 samples analyzed to date exhibit significant decoupling not only between Pt and Pd but also between Ru, Rh, and Ir. The best explanation for the decoupling is postmagmatic hydrothermal alteration, which affected not only silicates but also sulfides. The effects of postmagmatic alteration must be considered when using metal and isotopic ratios to evaluate primary mineralization. PGE variations in the remaining one third of the samples with Ir/(Ir + Ru) = 0.3–0.7, Ir/(Ir + Rh) = 0.4–0.8, and Pt/(Pt + Pd) = 0.3–0.7 indicate variable R-factors within individual ore bodies as well as the entire deposit, consistent with the interpretation that multiple sulfide-bearing magmas from depth were involved in the formation of the Jinchuan deposit. The mantle-normalized PGE patterns of the least-altered samples from the Jinchuan deposit are similar to the picrite-related Pechenga Ni-Cu sulfide deposit in Russia. PGE variations that can be related to sulfide liquid fractionation are observed in orebody-1 and orebody-24 but not in orebody-2 at Jinchuan. Exploration for Cu-, Pt-, and Pd-rich sulfide ores that may have been expelled into fractures in the footwalls of orebody-1 and orebody-24 appears to be justified.  相似文献   

20.
In the Great Dyke mafic/ultramafic layered intrusion of Zimbabwe, economic concentrations of platinum-group elements (PGE) are restricted to sulfide disseminations in pyroxenites of the Main Sulfide Zone (MSZ). Oxidized ores near the surface constitute a resource of ca. 400 Mt. Mining of this ore type has so far been hampered due to insufficient recovery rates. During the oxidation/weathering of the pristine ores, most notably, S and Pd are depleted, whereas Cu and Au are enriched. The concentrations of most other elements (including the other PGE) remain quite constant. In the oxidized MSZ, PGE occur in different modes: (1) as relict primary PGM (mainly sperrylite, cooperite, and braggite), (2) in solid solution in relict sulfides (dominantly Pd in pentlandite, up to 6,500 ppm Pd and 450 ppm Pt), (3) as secondary PGM neoformations (i.e., Pt–Fe alloy and zvyagintsevite), (4) as PGE oxides/hydroxides that replace primary PGM as the result of oxidation, (5) hosted in weathering products, i.e., iron oxides/hydroxides (up to 3,600 ppm Pt and 3,100 ppm Pd), manganese oxides/hydroxides (up to 1.6 wt.% Pt and 1,150 ppm Pd), and in secondary phyllosilicates (up to a few hundred ppm Pt and Pd). In the oxidized MSZ, most of the Pt and Pd are hosted by relict primary and secondary PGM; subordinate amounts are found in iron and manganese oxides/hydroxides. The amount of PGE hosted in solid solution in sulfides is negligible. Considerable local variations in the distribution of PGE in the oxidized ores complicate a mineralogical balance. Experiments to evaluate the PGE recovery from oxidized MSZ ore show that using physical concentration techniques (i.e., electric pulse disaggregation, hydroseparation, and magnetic separation), the PGE are preferentially concentrated into smaller grain size fractions by a factor of 2. Highest PGE concentrations occur in the volumetrically insignificant magnetic fraction. This indicates that a physical preconcentration of PGE is not feasible and that chemical, bulk-leaching methods need to be developed in order to successfully recover PGE from oxidized MSZ ore.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号