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1.
《Resource Geology》2018,68(3):209-226
Shin‐Otoyo, Suttsu, Teine, Date, Chitose, and Koryu are sites rich in precious and base metal Miocene–Pleistocene epithermal deposits, and located in southwestern Hokkaido, Japan. The deposits are predominantly hosted by the Green Tuff Formation of Middle Miocene age. Ore petrographic study of these deposits shows the occurrence of variable quantities of Cu–As–Sb–Ag–Bi–Pb–Te sulfosalt minerals. Determination of mineralogical and chemical compositions of the sulfosalt minerals was undertaken to elucidate the time and spatial changes of the sulfide‐sulfosalt minerals. Various types of sulfosalt minerals identified from gold–silver and base metal quartz–sulfide veins represented some sulfosalt mineralization phases, such as the Cu–Fe–Sn–S phase of mawsonite and stannite; Cu–(As,Sb)–S phase of tetrahedrite–tennantite and luzonite–famatinite series minerals; (Cu,Ag)–Bi–Pb–S phase of emplectite, pavonite, friedrichite, aikinite, and lillianite–gustavite series minerals; (Ag,Cu)–(As,Sb)–S phase of proustite–pyrargyrite and pearceite–polybasite series minerals; and Bi–Te–S phase of tetradymite and kawazulite minerals. There are some trends in the paragenetic sequence of sulfosalt mineralization in southwestern Hokkaido (in complete or partial) as follows: sulfide → Cu–Fe–Sn–S → (Cu,Ag)–Bi–Pb–S → (Bi–Te–S) → Cu–(As,Sb)–S → ([Ag,Cu]–[As,Sb]–S). The formation of sulfosalt minerals is characterized by the introduction of some elements such as Sn, Bi, and Te at an earlier stage and an increase or decrease of some elements such as As and Sb, followed by the introduction of Ag at the later stage of ore mineral paragenesis sequence. Mineral composition of the Chitose and Koryu deposits are slightly different from those of Shin‐Otoyo, Suttsu, Teine, and Date due to their lack of Sn (tin) and Bi (bismuth) mineralization. The variable concentrations and relationships are not simply with redistributed trace elements from the original sulfide minerals of chalcopyrite, pyrite, galena, and sphalerite. Some heavier elements were also introduced during the replacement reaction, which is consistent with the occurrence of their associated minerals.  相似文献   

2.
The Martabe Au–Ag deposit, North Sumatra Province, Indonesia, is a high sulfidation epithermal deposit, which is hosted by Neogene sandstone, siltstone, volcanic breccia, and andesite to basaltic andesite of Angkola Formation. The deposit consists of six ore bodies that occurred as silicified massive ore (enargite–luzonite–pyrite–tetrahedrite–tellurides), quartz veins (tetrahedrite–galena–sphalerite–chalcopyrite), banded sulfide veins (pyrite–tetrahedrite–sphalerite–galena) and cavity filling. All ore bodies are controlled by N–S and NW–SE trending faults. The Barani and Horas ore bodies are located in the southeast of the Purnama ore body. Fluid inclusion microthermometry, and alunite‐pyrite and barite‐pyrite pairs sulfur isotopic geothermometry show slightly different formation temperatures among the ore bodies. Formation temperature and salinity of fluid inclusions of the Purnama ore body range from 200 to 260 C and from 6 to 8 wt.% NaCl equivalent, respectively. Formation temperature and salinity of fluid inclusions of the Barani ore body range from 200 to 220 °C and from 0 to 2.5 wt.% NaCl equivalent and those of the Horas ore body range from 240 to 275 °C and from 2 to 3 wt.% NaCl equivalent, respectively. The Barani and Horas ore bodies are less silicified and sulfides are less abundant than the Purnama ore body. A relationship between enthalpy and chloride content indicates mixing of hot saline fluids with cooler dilute fluids during the mineralization of each of the ore bodies. The δ18O values of quartz samples from the southeast ore bodies exhibit a wide range from +4.2 to +12.9‰ with an average value of +7.0‰. The δ18O values of H2O estimated from δ18O values of quartz, barite and calcite confirm the oxygen isotopic shift to near meteoric water trend, which support the incorporation of meteoric water. Salinity of the fluid inclusions decrease from >5 wt.% NaCl equivalent in the Purnama ore body to <3 wt.% NaCl equivalent in the Barani ore body, indicating different fluid systems during mineralization. The δ34S values of sulfide and sulfate in Purnama range from ? 4.2 to +5.5‰ and from +1.2 to +26.7‰, those in the Barani range from ? 4.3 to +26.4‰ and from +3.9 to +18.5‰ and those in the Horas ore body range from ? 11.8 to +3.5‰ and from +1.4 to +25.7‰, respectively. The δ34S of total bulk sulfur in southeastern ore bodies (Σδ34S) was estimated to be approximately +6‰. The estimated sulfur fugacity during formation of the Purnama and Horas ore bodies is relatively high. It was between 10?4.8 and 10?10.8 atm at 220 to 260 °C. Tellurium fugacity was between 10?7.8 and 10?9.5 atm at 260 °C and between 10?9 and 10?10.6 atm at 220 °C in the Purnama ore body. The Barani ore body was formed at lower fS2, lower than about 10?14 atm at 200 to 220 °C based on the presence of arsenopyrite and pyrrhotite in the early stage, and between 10?14 and 10?12 atm based on the existence of enargite and tennantite in the last stage. © 2016 The Society of Resource Geology  相似文献   

3.
Sulfide and sulfate ore samples collected from the Hakurei deposit of the Bayonnaise knoll were examined for the occurrence and chemical composition of minerals, including the sulfur isotopes and the microthermometry of fluid inclusions. Massive sulfide ore, mineralized volcanic rock, and anhydrite ore occur in descending order, from the seafloor to the bottom of the cored sample. The massive sulfide ore is dominated by sphalerite and accompanied by tennantite, chalcopyrite, and pyrite with lesser amounts of galena, enargite, and covellite. Amorphous silica is commonly precipitated on the surface of the sulfide minerals. As‐bearing minerals such as tennantite, enargite, and luzonite are common, while galena and Sb‐rich tetrahedrite are scarce. The mineral abundance and chemical composition of the minerals differs from that found in chimneys of the deposit. The sulfur isotope compositions in the minerals are +3.1–5.2‰ for sulfides and +19.6–21.8‰ for sulfate minerals. The homogeneous nature of the sulfur isotopes suggests that sulfur incorporated in the Hakurei deposit came from the reduction of aqueous sulfate in seawater.  相似文献   

4.
Abstract: The Lepanto Far Southeast porphyry Cu‐Au deposit is located beneath and to the southeast of the Lepanto enargite‐luzonite Cu–Au deposit in Mankayan, Benguet Province, Philippines. The principal orebody consists of potassic alteration subjected to partial retrograde chlorite alteration that rims stock‐work of quartz‐anhydrite veinlets. Fluid inclusions found in stockwork quartz and anhydrite in the biotitized orebody center are dominated by polyphase inclusions that homogenize at temperatures of >500C. Sulfur isotopic thermometry applied to the sulfides‐anhydrite pairs suggests around 500C. The principal ore minerals associated with quartz‐anhydrite stockworks are chalcopyrite and pyrite with minor bornite and Bi–Te–bearing tennantite, with trace of native gold. Rounded pyrite grains appear fractured and corroded and are interpreted as remnants of primary intermediate solid solution + pyrite assemblage. A breccia pipe truncates the deposit. Mineralization in the breccia pipe is brought by quartz‐anhydrite veinlets and infilling in the interstices between clasts. Chalcopyrite‐Au mineralization associated with molybdenite is recognized in the deeper zone in the breccia pipe. Fluid inclusion microthermometry on polyphase inclusions in veinlet quartz as well as sulfur isotope thermometry applied for the pair of anhydrite and sulfides suggests >450C. Fluid inclusions in veinlet quartz and anhydrite in the fringe advanced argillic alteration are chiefly composed of coexisting liquid‐rich inclusions and gas‐rich inclusions, in addition to coexisting polyphase inclusions and gas‐rich inclusions. These inclusions exhibit a wide range of homogenization temperatures, suggesting heterogeneous entrapping in the two‐fluid unmixing region. Sulfur isotopes of aqueous sulfide and sulfate exhibit a general trend from the smallest fractionation pairs (about 11%) in the biotitized orebody center to the largest fractionation (about 25%) pairs in the fringe advanced argillic alteration, suggesting a simple evolution of hydrothermal system. The slopes of arbitrary regression lines in δ34S versus 34S[SO4 = –H2S] diagram suggest that the abundance ratio of aqueous sulfate to sulfide in the hydrothermal fluid has been broadly constant at about 1:3 through temperature decrease. The intersection of these two regression lines at the δ34S axis indicates that the bulk δ34S is about +6%. Thus, the Lepanto FSE deposit is a further example which confirms enrichment in 34S in the hydrous intermediate to silicic magmas and associated magmatic hydrothermal deposits in the western Luzon arc.  相似文献   

5.
The world‐class Far Southeast (FSE) porphyry system, Philippines, includes the FSE Cu–Au porphyry deposit, the Lepanto Cu–Au high‐sulfidation deposit and the Victoria–Teresa Au–Ag intermediate‐sulfidation veins, centered on the intrusive complex of dioritic composition. The Lepanto and FSE deposits are genetically related and both share an evolution characterized by early stage 1 alteration (deep FSE potassic, shallow Lepanto advanced argillic‐silicic, both at ~1.4 Ma), followed by stage 2 phyllic alteration (at ~1.3 Ma); the dominant ore mineral deposition within the FSE porphyry and the Lepanto epithermal deposits occurred during stage 2. We determined the chemical and S isotopic composition of sulfate and sulfide minerals from Lepanto, including stage 1 alunite (12 to 28 permil), aluminum–phosphate–sulfate (APS) minerals (14 to 21 permil) and pyrite (?4 to 2 permil), stage 2 sulfides (mainly enargite–luzonite and some pyrite, ?10 to ?1 permil), and late stage 2 sulfates (barite and anhydrite, 21 to 27 permil). The minerals from FSE include stage 2 chalcopyrite (1.6 to 2.6 permil), pyrite (1.1 to 3.4 permil) and anhydrite (13 to 25 permil). The whole‐rock S isotopic composition of weakly altered syn‐mineral intrusions is 2.0 permil. Stage 1 quartz–alunite–pyrite of the Lepanto lithocap, above about 650 m elevation, formed from acidic condensates of magmatic vapor at the same time as hypersaline liquid formed potassic alteration (biotite) near sea level. The S isotopic composition of stage 1 alunite–pyrite record temperatures of approximately 300–400°C for the vapor condensate directly over the porphyry deposit; this cooled to <250°C as the acidic condensate flowed to the NW along the Lepanto fault where it cut the unconformity at the top of the basement. Stage 1 alunite at the base of the advanced argillic lithocap over FSE contains cores of APS minerals with Sr, Ba and Ca; based on back‐scattered electron images and ion microprobe data, these APS minerals show a large degree of chemical and S‐isotopic heterogeneity within and between samples. The variation in S isotopic values in these finely banded stage 1 alunite and APS minerals (16 permil range), as well as that of pyrite (6 permil range) was due largely to changes in temperature, and perhaps variation in redox conditions (average ~ 2:1 H2S:SO4). Such fluctuations could have been related to fluid pulses caused by injection of mafic melt into the diorite magma chamber, supported by mafic xenoliths hosted in diorite of an earlier intrusion. The S isotopic values of stage 2 minerals indicate temperatures as high as 400°C near sea level in the porphyry deposit, associated with a relatively reduced fluid (~10:1 H2S:SO4) responsible for deposition of chalcopyrite. Stage 2 fluids were relatively oxidized in the Lepanto lithocap, with an H2S:SO4 ratio of about 4. The oxidation resulted from cooling, which was caused by boiling during ascent and then dilution with steam‐heated meteoric water in the lithocap. This cooling also resulted in the sulfidation state of minerals increasing from chalcopyrite stability in the porphyry deposit to that of enargite in the lithocap‐hosted high‐sulfidation deposit. The temperature at the base of the lithocap during stage 2 was ≥300°C, cooling to <250°C within the main lithocap, and about 200°C towards the limit of the Lepanto orebody, approximately 2 km NW of the porphyry deposit. Approximate 300°C and 200°C isotherms, estimated from S isotopic and fluid inclusion temperatures during stage 1 and stage 2, shifted towards the core of the FSE porphyry deposit with time. This general retreat in isotherms was more than 500 m laterally within Lepanto and 500 m vertically within FSE as the magmatic–hydrothermal system evolved and collapsed over the magmatic center. During this evolution, there is also evidence recorded by large S isotopic variations in individual crystals for sharp pulses of higher temperature, relatively reduced fluid injected into the porphyry deposit.  相似文献   

6.
青海玉树地区东莫扎抓铅锌矿床位于青藏高原金沙江缝合带和班公湖-怒江缝合带夹持的羌塘地体东北缘,是"三江"北段铜铅锌多金属成矿带铅锌矿床的典型代表。在野外地质观察基础上,本文对矿石矿物和重晶石进行了S同位素组成分析,对矿石矿物、脉石矿物和区域地层进行了Pb同位素组成分析,对脉石矿物进行了Sr-Nd同位素组成分析。结果表明,硫化物δ34S值为-29‰~6‰,峰值为-8‰~-6‰,反映了总体富轻硫的特征,而重晶石δ34S值为18.3‰~+22.8‰,来自于第三纪陆相盆地。宽的δ34S变化可以解释为流体在盆地内活动期间与不同地层单元发生相互作用,从而继承了不同物质单元的S同位素特点,还原硫应主要来自于硫酸盐的细菌还原或者含硫有机质的热还原,反映硫来自沉积盆地。矿石矿物的206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.387~18.703、15.391~15.768、38.372~38.809,而脉石矿物的206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.423~18.612、15.491~15.701、38.497~38.612。矿石矿物和脉石矿物的Pb同位素组成介于区域上地壳Pb组成范围内,总体类似于MVT矿床,显示Pb等金属元素来源于上地壳岩石。脉石矿物的(87Sr/86Sr)ⅰ、εSr(t)、(143Nd/144Nd)ⅰ和εNd(t)分别为0.70855~0.70928、58.0~68.4、0.512273~0.512353、-6.2~-4.7。Sr-Nd同位素特征亦显示脉石矿物的物质来源于上地壳岩石。  相似文献   

7.
Abstract. The Nena Cu‐Au deposit, located in the Frieda River mineral district of northwestern mainland Papua New Guinea, is a composite structurally‐lithologically controlled high sulfidation (HS) system. Its hydrothermal alteration and Cu‐Au mineralization are presented in this paper. Initially propylitized andesitic volcanics veined by epithermal quartz were pervasively superimposed by zoned HS alteration. The zonation grades from vuggy silica core to sulfur‐rich, pyritic silica‐alunite halo followed by pyrophyllite‐dickite‐kaolinite interval and finally to thin illite‐smectite margin, suggesting progressive decrease in temperature and increase in pH. This zonation is enveloped by chlorite‐epidote‐calcite‐gypsum alteration. The acid altered rocks were then invaded by multiple phases of pyrite, subsequently crosscut by quartz, vein alunite and barite. Then sequential deposition of bladed covellite, enargite, luzonite and stibioluzonite occurred from the NW to the SE portions of the deposit, forming a zonation suggestive of progressive decrease in temperature, sulfur fugacity and sulfidation stage. Most ore mineralization occurs in the vuggy silica core. Gold mineralization commenced from the transition of enargite to luzonite and continued throughout the stibioluzonite stage. Associated with gold deposition are Au‐rich pyrite, tennantite‐tetrahedrite, chalcopyrite‐bornite, native tellurium, electrum, calaverite, bismuthinite and galena. Native sulfur occupied the remaining cavities and represents the waning stage of the hydrothermal system. Fluid inclusions studies distinguished magmatic (>300–350d?C, 9–15 wt% NaCl equiv.) and meteoric (<150–200d?C, 1–2 wt% NaCl equiv.) fluids (Holzberger et al., 1996). Temperatures and salinities of fluid inclusions from barite associated with Cu sulfides show a general decrease from NW (330d?C, 9–15 wt% NaCl equiv.) to SE (172d?C, 10 wt% NaCl equiv.) parts of the deposit, indicating gradual entrainment of ground water (Hitchman and Espi, 1997). Interaction of magmatic fluids with meteoric water accompanied by changes in temperature, salinity, acidity and oxidation state of the resultant fluids is interpreted to have been the main cause of metal precipitation. Finally, supergene processes generated Au zone with an underlying chalcocite‐covellite‐digenite blanket over the primary sulfides at depth. Gold occurs as lattice constituent in scorodite, limonite‐goethite and jarosite. Chalcocite is more abundant and widespread than other Cu sulfides. Acidic fluids deposited powdery alunite and kaolinite, vein alunite and amorphous silica. Weakly secondary biotite‐quartz altered porphyry located below the known HS Cu‐Au deposit contains chalcopyrite‐bornite and is overprinted by quartz‐alunite‐pyro‐phyllite‐pyrite assemblage. This feature indicates close temporal, spatial and genetic relation between the two deposit types.  相似文献   

8.
Abstract: Mineral paragenesis of the alteration, ore and gangue minerals of the Lepanto epithermal copper‐gold deposit and the Victoria gold deposit, Mankayan Mineral District, Northern Luzon, Philippines, is discussed. The principal ore minerals of the Lepanto copper‐gold deposit are enargite and luzonite, with significant presence of tennantite‐tetrahedrite, chalcopyrite, sphalerite, galena, native gold/electrum and gold‐silver tellurides. Pervasive alteration zonations are commonly observed from silicification outward to advanced argillic then to propylitic zone. The ore mineralogy of the Lepanto copper‐gold deposit suggests high fS2 in the early stages of mineralization corresponding to the deposition of the enargite‐luzonite‐pyrite assemblage. Subsequent decrease in the fS2 formed the chalcopyrite‐tennantite‐pyrite assemblage. An increase in the fS2 of the fluids with the formation of the covellite‐digenite‐telluride assemblage caused the deposition of native gold/electrum and gold‐silver tellurides. The principal ore minerals of the Victoria gold deposit are sphalerite, galena, chalcopyrite, tetrahedrite and native gold/electrum. The alteration halos are relatively narrow and in an outward sequence from the ore, silica alteration grades to illitic‐argillic alteration, which in turn grades to propylitic alteration. The Victoria gold mineralization has undergone early stages of silica supersaturation leading to quartz deposition. Vigorous boiling increased the pH of the fluids that led to the deposition of sulfides and carbonates. The consequent decrease in H2S precipitated the gold. Gypsum and anhydrite mainly occur as overprints that cut the carbonate‐silica stages. The crosscutting and overprinting relationships of the Victoria quartz‐gold‐base metal veins on the Lepanto copper‐gold veins manifest the late introduction of near neutral pH hydrothermal fluids.  相似文献   

9.
Mineral assemblages, chemical compositions of ore minerals, wall rock alteration and fluid inclusions of the Gatsuurt gold deposit in the North Khentei gold belt of Mongolia were investigated to characterize the gold mineralization, and to clarify the genetic processes of the ore minerals. The gold mineralization of the deposit occurs in separate Central and Main zones, and is characterized by three ore types: (i) low‐grade disseminated and stockwork ores; (ii) moderate‐grade quartz vein ores; and (iii) high‐grade silicified ores, with average Au contents of approximately 1, 3 and 5 g t?1 Au, respectively. The Au‐rich quartz vein and silicified ore mineralization is surrounded by, or is included within, the disseminated and stockwork Au‐mineralization region. The main ore minerals are pyrite (pyrite‐I and pyrite‐II) and arsenopyrite (arsenopyrite‐I and arsenopyrite‐II). Moderate amounts of galena, tetrahedrite‐tennantite, sphalerite and chalcopyrite, and minor jamesonite, bournonite, boulangerite, geocronite, scheelite, geerite, native gold and zircon are associated. Abundances and grain sizes of the ore minerals are variable in ores with different host rocks. Small grains of native gold occur as fillings or at grain boundaries of pyrite, arsenopyrite, sphalerite, galena and tetrahedrite in the disseminated and stockwork ores and silicified ores, whereas visible native gold of variable size occurs in the quartz vein ores. The ore mineralization is associated with sericitic and siliceous alteration. The disseminated and stockwork mineralization is composed of four distinct stages characterized by crystallization of (i) pyrite‐I + arsenopyrite‐I, (ii) pyrite‐II + arsenopyrite‐II, (iii) galena + tetrahedrite + sphalerite + chalcopyrite + jamesonite + bournonite + scheelite, and iv) boulangerite + native gold, respectively. In the quartz vein ores, four crystallization stages are also recognized: (i) pyrite‐I, (ii) pyrite‐II + arsenopyrite + galena + Ag‐rich tetrahedrite‐tennantite + sphalerite + chalcopyrite + bournonite, (iii) geocronite + geerite + native gold, and (iv) native gold. Two mineralization stages in the silicified ores are characterized by (i) pyrite + arsenopyrite + tetrahedrite + chalcopyrite, and (ii) galena + sphalerite + native gold. Quartz in the disseminated and stockwork ores of the Main zone contains CO2‐rich, halite‐bearing aqueous fluid inclusions with homogenization temperatures ranging from 194 to 327°C, whereas quartz in the disseminated and stockwork ores of the Central zone contains CO2‐rich and aqueous fluid inclusions with homogenization temperatures ranging from 254 to 355°C. The textures of the ores, the mineral assemblages present, the mineralization sequences and the fluid inclusion data are consistent with orogenic classification for the Gatsuurt deposit.  相似文献   

10.
The Cangyuan Pb-Zn-Ag polymetallic deposit is located in the Baoshan Block, southern Sanjiang Orogen. The orebodies are hosted in low-grade metamorphic rocks and skarn in contact with Cenozoic granitic rocks. Studies on fluid inclusions (FIs) of the deposit indicate that the ore-forming fluids are CO2-bearing, NaCl-H2O. The initial fluids evolved from high temperatures (462–498 °C) and high salinities (54.5–58.4 wt% NaCl equiv) during the skarn stage into mesothermal (260–397 °C) and low salinities (1.2–9.5 wt% NaCl equiv) during the sulfide stage. The oxygen and hydrogen isotopic compositions (δ18OH2O: 2.7–8.8‰; δD: −82 to −120‰) suggest that the ore-forming fluids are mixture of magmatic fluids and meteoric water. Sulfur isotopic compositions of the sulfides yield δ34S values of −2.3 to 3.2‰; lead isotopic compositions of ore sulfides are similar to those of granitic rocks, indicating that the sulfur and ore-metals are derived from the granitic magma. We propose that the Cangyuan Pb-Zn-Ag deposit formed from magmatic hydrothermal fluids. These Cenozoic deposits situated in the west of Lanping-Changdu Basin share many similarities with the Cangyuan in isotopic compositions, including the Laochang, Lanuoma and Jinman deposits. This reveals that the Cenozoic granites could have contributed to Pb-Zn-Cu mineralization in the Sanjiang region despite the abundance of Cenozoic Pb-Zn deposits in the region, such as the Jingding Pb-Zn deposit, that is thought to be of basin brine origin.  相似文献   

11.
梅微  吕新彪  王祥东  范谢均  魏巍 《地球科学》2020,45(12):4428-4445
大兴安岭南段黄岗铁锡多金属矿床具有明显的蚀变-矿化特征,对于研究矽卡岩型矿床的成矿过程具有重要的意义.因此对该矿床中具有代表性的蚀变矿物以及金属矿物开展电子探针研究,结果指示研究区的热液演化经历了4个阶段:在进变质矽卡岩阶段（Ⅰ）,矿物以含有钙铁榴石GrtⅠ核的钙铝榴石GrtⅡ和钙铁辉石为主;在退变质矽卡岩阶段（Ⅱ）,矿物以富铁榴石GrtⅢ、浸染状磁铁矿以及含水矿物为代表;氧化物阶段（Ⅲ）的矿物以大量磁铁矿、锡石以及少量钙铁榴石GrtⅣ和透辉石为主;在硫化物阶段（Ⅳ）,磁铁矿逐渐被硫化物交代,最后形成毒砂、黄铁矿、黄铜矿、铁闪锌矿、浅色闪锌矿-黄铜矿-方黝锡矿固溶体、锑黝铜矿等,表明黄岗铁多金属矿床的流体来源从岩浆水、交代流体最后演化为大气降水的加入,流体成分变化复杂,流体演化具体表现为温度逐渐降低,水岩比值逐渐升高,具有还原性→氧化性→还原性等特点.   相似文献   

12.
白秧坪银铜多金属矿集区位于兰坪盆地北部。矿集区可分为东、西两个成矿带。赋矿地层主要为上三叠统三合洞组碳酸盐岩、第三系始新统保相寺组碎屑岩和下白垩统景星组碎屑岩。矿体主要以脉状、网脉状及透镜状形式产出。作者通过显微镜观察、电子探针和扫描分析等综合分析技术,确认白秧坪银铜多金属矿集区中矿物组成相当丰富,已鉴定出的矿物超过50种,既有大量硫化物、硫盐、氧化物、硫酸盐、碳酸盐,又有自然金属及金属互化物、卤化物等。除常见矿物为黄铁矿、毒砂、白铁矿、黄铜矿、方铅矿、闪锌矿、黝铜矿、砷黝铜矿、铜蓝、斑铜矿、辉铜矿、雌黄、菱铁矿、方解石、铁白云石、重晶石、天青石和石英外,作者还鉴定出一些银、钴、铋、镍、砷、锑的矿物,如自然铋、辉铋矿、辉银矿、辉砷钴矿、硫钴镍矿、硫铜铋矿、硫铋铜矿、辉砷镍矿、车轮矿、硫砷铜矿、单斜硫砷铅矿、灰硫砷铅矿等。矿石中矿物种类较多,组成较复杂,存在Co,Bi,Ni等元素的矿物,构成白秧坪银铜多金属矿集区的一大特色。在兰坪盆地白秧坪银铜多金属矿集区各矿段内,除了Cu、Pb、Zn构成工业矿体外,矿石中Ag、Co、Ni、Bi及As、Sb、Ba等元素的含量也相当高,可作为Cu-Pb-Zn-Ag-Co-Ni-Bi矿石来综合开发利用。白秧坪银铜多金属矿集区中Ag、Co、Ni、Bi等元素富集条件为低温、中低盐度,形成压力较小的浅成环境;成矿流体是一种富含CO2的Ca2+-Na+-SO24-Cl-类型、由大气降水演化而成的盆地热卤水。成矿物质主要来源于含有基性火山岩的兰坪盆地基底变质岩系。  相似文献   

13.
《Resource Geology》2018,68(3):258-274
The Dabaoshan deposit in Northern Guangdong Province, South China, is a Cu–Mo–W–Pb–Zn polymetallic deposit, located in the southern part of the Qin–Hang porphyry–skarn Cu–Mo ore belt. The deposit mainly comprises porphyry Mo and stratiform skarn Cu ore deposits. The genesis of the Cu ore deposit has been ascribed to a typical skarn ore deposit formed by the metasomatism of Devonian carbonate rock layers or to a volcanic rock‐hosted massive sulfide deposit formed by marine exhalation. In this paper, we report on the homogenization temperatures and salinities of fluid inclusions and C, H, O, S, and Pb isotopic compositions of fluids and minerals in this deposit. Homogenization temperatures and salinities of fluid inclusions in garnet, diopside, quartz, and calcite provide information on the skarnification, mineralization, and postmineralization stages. The data show that ore‐forming fluids experienced a continuous transition from high temperatures and salinities to low temperatures and salinities over the entire period of mineralization. C, H, and O isotopic compositions indicate that ore‐forming fluids were derived mainly from magmatic water. O isotopic compositions indicate that ore‐forming fluids mingled with atmospheric water during the last stage of mineralization. Sulfur in the ore came mainly from deep magmatic sources. Pb isotopic compositions in the orebody show that almost all the lead in the ore was derived from magma with a crustal source. Combined geological, geophysical, and geochemical data were achieved before we proposed that the Dabaoshan porphyry–skarn Cu–Mo–W–Pb–Zn deposit, as one member of the Qin–Hang porphyry–skarn Cu–Mo ore belt, formed during the Jurassic subduction of the paleo‐Pacific plate beneath the Eurasian continent at quite low angle. NE‐ and EW‐trending structures controlled the emplacement of magmatic rocks in the South China region. In the mining area, the Xiangguanping Fault and its branches were the main conduits for magmatic crystallization and mineralization. The many subfaults, folds, and interlayer fracture zones on both sides of the main fault provided the requisite space for the ore and, together, were the controlling structures of the orebody.  相似文献   

14.
The paper considers the results of high-precision Pb–Pb isotopic analysis of 120 galena samples from 27 Au and Ag deposits of the South Verkhoyansk Synclinorium (SVS) including large Nezhdaninsky deposit (628.8 t Au). The Pb isotopic composition is analyzed on a MC-ICP-MS NEPTUNE mass-spectrometer from solutions with an error of no more than ±0.02% (2σ). Four types of deposits are studied: (i) stratified vein gold–quartz deposits (type 1) hosted in metamorphosed Upper Carboniferous–Lower Permian terrigenous rocks and formed during accretion of the Okhotsk Block to the North Asian Craton synchronously with dislocation metamorphism and related granitic magmatism; (ii) vein gold–quartz (Nezhdaninsky type) deposits also hosted in Lower Permian metasedimentary rocks; (iii) Au–Bi deposits localized at the contact zones of the Late Cretaceous granitic plutons; and (iv) Sn–Ag polymetallic deposits related to granitic and subvolcanic rocks of the Okhotsk Zone of the SVS. The deposits of types 2, 3, and 4 are postaccretionary. The general range of 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios is 18.1516–18.5903 (2.4%), 15.5175–15.6155 (0.63%), and 38.3010–39.0481 (2.0%), respectively. In 206Pb/204Pb–207Pb/204Pb and 206Pb/204Pb–208Pb/204Pb diagrams, the data points of Pb isotopic compositions of all deposits occupy restricted, partly overlapping areas along a general elongated trend. The various SVS Au–Ag deposits can be classified according to the Pb isotopic composition in accordance with all three Pb ratios. Deposits of the same type show distinct Pb isotopic compositions that strongly exceed the scale of analytical error (±0.02%). The differences in Pb isotopic composition within specific deposits are low and subordinate and have little effect on variations in the Pb isotopic composition of the SVS deposits. The μ2 values (Stacey–Kramers model), which characterize the 238U/204Pb ratios of ore lead sources of the SVS deposits, widely vary from 9.7 to 9.38. The ω2 values (232Th/204Pb) are 39.82–36.61, whereas the Th/U ratios are 4.04–3.86. The content of all three radiogenic Pb isotopes and μ2 values of feldspars from SVS intrusive rocks are strongly distinct from those of galena of stratified gold–quartz and vein gold–quartz deposits and are identical to Pb of galena from Au–Bi and Sn–Ag polymetallic deposits, indicating a mostly magmatic origin for the Pb of these deposits. Detailed isotopic study of the Nezhdaninsky deposit shows different Pb isotopic composition of two consecutive mineral assemblages (gold–sulfide and Ag polymetallic): ~0.30, ~0.07, and ~0.22% for 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios, respectively. These differences are interpreted as a result of involvement of at least two metal sources during the evolution of an ore-forming system: (i) host Lower Permian terrigenous rocks and (ii) a magmatic source similar in Pb isotopic composition to that of Sn–Ag polymetallic deposits. The Pb isotopic composition and μ2 and Th/U values show that lead of stratified gold–quartz deposits combines isotopic tracers of lower and upper crustal sources (Upper Carboniferous–Lower Permian terrigenous rocks), lead of which was mobilized by ore-bearing fluids. The high 208Pb/206Pb ratios and Th/U evolutionary parameter are common to all Pb isotopic composition of all studied Au–Ag deposits and SVS Cretaceous intrusive rocks and indicate that Pb sources were depleted in U relative to Th. Taking into account the structure of the region and conceptions on its evolution, we can suggest that the magma source was related to lower crustal subducted rocks of the Archean (~2.6 Ga) North Asian Craton and the Okhotsk terrane.  相似文献   

15.
为了进一步理解华南下寒武统Ni-Mo-Se多金属层的物质来源及形成环境,文中分析了遵义中南村和张家界后坪两个Ni-Mo-Se矿层及其围岩的黄铁矿硫同位素和全岩的硒同位素组成。硫同位素组成显示两个Ni-Mo-Se矿层形成时的环境存在区域性差别,中南村矿层形成于间歇开放的海洋环境,而后坪矿层形成于封闭的缺氧(静海)环境。较大的硫同位素范围暗示硫酸盐还原菌控制硫同位素的分馏,而热液流体可能提供了大量金属元素,从而导致矿层富集大量的硫化物和稀有金属。硒同位素组成指示牛蹄塘组底部热液流体的Se可能重新经历了氧化还原循环,而Se的富集过程可能受有机质和粘土矿物吸附或类质同象过程控制。因此,控制多金属富集的因素主要为富集金属的热液流体的参与和缺氧环境下的自生沉积。  相似文献   

16.
The Pingüino deposit, located in the low sulfidation epithermal metallogenetical province of the Deseado Massif, Patagonia, Argentina, represents a distinct deposit type in the region. It evolved through two different mineralization events: an early In-bearing polymetallic event that introduced In, Zn, Pb, Ag, Cd, Au, As, Cu, Sn, W and Bi represented by complex sulfide mineralogy, and a late Ag–Au quartz-rich vein type that crosscut and overprints the early polymetallic mineralization. The indium-bearing polymetallic mineralization developed in three stages: an early Cu–Au–In–As–Sn–W–Bi stage (Ps1), a Zn–Pb–Ag–In–Cd–Sb stage (Ps2) and a late Zn–In–Cd (Ps3). Indium concentrations in the polymetallic veins show a wide range (3.4 to 1,184 ppm In). The highest indium values (up to 1,184 ppm) relate to the Ps2 mineralization stage, and are associated with Fe-rich sphalerites, although significant In enrichment (up to 159 ppm) is also present in the Ps1 paragenesis associated with Sn-minerals (ferrokesterite and cassiterite). The hydrothermal alteration associated with the polymetallic mineralization is characterized by advanced argillic alteration within the immediate vein zone, and sericitic alteration enveloping the vein zone. Fluid inclusion studies indicate homogenisation temperatures of 308.2–327°C for Ps1 and 255–312.4°C for Ps2, and low to moderate salinities (2 to 5 eq.wt.% NaCl and 4 to 9 eq.wt.% NaCl, respectively). δ34S values of sulfide minerals (+0.76‰ to +3.61‰) indicate a possible magmatic source for the sulfur in the polymetallic mineralization while Pb isotope ratios for the sulfides and magmatic rocks (206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of 17.379 to 18.502; 15.588 to 15.730 and 38.234 to 38.756, respectively) are consistent with the possibility that the Pb reservoirs for both had the same crustal source. Spatial relationships, hydrothermal alteration styles, S and Pb isotopic data suggest a probable genetic relation between the polymetallic mineralization and dioritic intrusions that could have been the source of metals and hydrothermal fluids. Mineralization paragenesis, alteration mineralogy, geochemical signatures, fluid inclusion data and isotopic data, confirm that the In-bearing polymetallic mineralization from Pingüino deposit is a distinct type, in comparison with the well-known epithermal low sulfidation mineralization from the Deseado Massif.  相似文献   

17.
安徽铜陵姚家岭锌金多金属矿床成岩成矿年代学研究   总被引：10，自引：5，他引：5  
姚家岭锌金多金属矿床位于铜陵断隆区与繁昌断凹区的过渡部位,是长江中下游成矿带新近发现的大型锌金多金属矿床,也是铜陵矿集区中迄今发现的首例大型锌金多金属矿床。在详细野外地质工作及室内研究的基础上,对姚家岭矿床花岗闪长斑岩体开展了LA-ICPMS锆石U-Pb定年工作,获得206Pb/238U加权平均年龄为141.4±1.7Ma(MSWD=0.78,n=19),代表成岩年龄;选取了该矿床金属矿物辉钼矿进行Re-Os同位素测年,获得模式年龄范围为141.2±2.1Ma~141.6±2.7Ma,平均年龄为141.4±2.4Ma,可代表热液成矿作用的时代,与成岩年龄一致。姚家岭锌金多金属矿床为早白垩世早期岩浆热液作用形成的,是铜陵断隆区燕山期大规模成矿作用的产物,铜陵断隆区具有进一步寻找锌金矿床的有利前景。  相似文献   

18.
The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ34S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ34S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones.  相似文献   

19.
西藏甲玛铜多金属矿硫同位素地球化学研究   总被引：1，自引：0，他引：1  
西藏墨竹工卡县甲玛铜多金属矿床位于冈底斯成矿带东段,Cu、Mo、Pb+Zn、Au、Ag均达大型规模,并伴生Co、Bi、W、Ni等多金属矿化。黄铜矿、斑铜矿、辉钼矿、方铅矿、闪锌矿、黝铜矿、辉铜矿等硫化物为主要的矿石矿物,硫酸盐矿物以硬石膏为主,含矿岩浆岩以花岗斑岩、二长花岗斑岩和花岗闪长斑岩为主。通过对甲玛矿区主要硫化物和硬石膏的硫同位素分析,并结合前人研究,甲玛矿区硫化物的硫同位素δ34S值变化于13.6‰～+12.5‰,平均值1.33‰(样品数86)、硬石膏δ34S值+0.5‰～+1.8‰,平均值+1.13‰(样品数3)、岩浆岩δ34S值0.7‰～0.2‰,平均值0.5‰(样品数3),与岩浆硫δ34S值0±3‰一致。闪锌矿-方铅矿-黄铜矿矿物对的硫同位素地质温度计,显示成矿温度为408～433℃,说明其形成时硫同位素处于平衡状态。冈底斯成矿带上的驱龙等斑岩型矿床中硫化物和岩浆岩硫同位素,均具有δ34S值变化范围小,平均值接近0值,与岩浆硫特征一致的特点,反映了甲玛铜多金属矿床具有矽卡岩-斑岩型矿床硫同位素地球化学特征,硫以岩浆来源为主。  相似文献   

20.
Abstract. The Yuryang gold deposit, comprising a Te‐bearing Au‐Ag vein mineralization, is located in the Cheonan area of the Republic of Korea. The deposit is hosted in Precambrian gneiss and closely related to pegmatite. The mineralized veins display massive quartz textures, with weak alteration adjacent to the veins. The ore mineralization is simple, with a low Ag/Au ratio of 1.5:1, due to the paucity of Ag‐phases. Ore mineralization took place in two different mineral assemblages with paragenetic time; early Fe‐sulfide mineralization and late Fe‐sulfide and Au‐Te mineralization. The early Fe‐sulfide mineralization (pyrite + sphalerite) occurred typically along the vein margins, and the subsequent Au‐Te mineralization is characterized by fracture fillings of galena, sphalerite, pyrrhotite, Te‐bearing minerals (petzite, altaite, hessite and Bi‐Te mineral) and electrum. Fluid inclusions characteristically contain CO2 and can be classified into four types (Ia, Ib, IIa and IIb) according to the phase behavior. The pressure corrected temperatures (≥500d?C) indicate that the deposit was formed at a distinctively high temperature from fluids with moderate to low salinity (<12 wt% equiv. NaCl) and CH4 (1?22 mole %). The sphalerite geo‐barometry yield an estimated pressure about 3.5 ?2.1 kbar. The dominant ore‐deposition mechanisms were CO2 effervescence and concomitant H2S volatilization, which triggered sulfidation and gold mineralization. The measured and calculated isotopic compositions of fluids (δ18OH2O = 10.3 to 12.4 %o; δDH2O = ‐52 to ‐77 %o) may indicate that the gold deposition originated from S‐type magmatic waters. The physicochemical conditions observed in the Yuryang gold deposit indicate that the Jurassic gold deposits in the Cheonan area, including the Yuryang gold deposit are compatible with deposition of the intrusion‐related Au‐Te veins from deeply sourced fluids generated by the late Jurassic Daebo magmatism.  相似文献   

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