Telescoped porphyry Cu-Mo-Au mineralisation, advanced argillic alteration and quartz-sulphide-gold-anhydrite veins in the Thames District, New Zealand

Porphyry Cu-Mo-Au mineralisation with associated potassic and phyllic alteration, an advanced argillic alteration cap and epithermal quartz-sulphide-gold-anhydrite veins, are telescoped within a vertical interval of 400-800 m on the northeastern margin of the Thames district, New Zealand. The geological setting is Jurassic greywacke basement overlain by Late Miocene andesitic-dacitic rocks that are extensively altered to propylitic and argillic assemblages. The porphyry Cu-Mo-Au mineralisation is hosted in a dacite porphyry stock and surrounding intrusion breccia. Relicts of a core zone of potassic K-feldspar-magnetite-biotite alteration are overprinted by phyllic quartz-sericite-pyrite or intermediate argillic chlorite-sericite alteration assemblages. Some copper occurs in quartz-magnetite-chlorite-pyrite-chalcopyrite veinlets in the core zone, but the bulk of the copper and the molybdenum are associated with the phyllic alteration as disseminated chalcopyrite and as molybdenite-sericite-carbonate veinlets. The advanced argillic cap has a quartz-alunite-dickite core, which is enveloped by an extensive pyrophyllite-diaspore-dickite-kaolinite assemblage that overlaps with the upper part of the phyllic alteration zone. Later quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins occur within and around the margins of the porphyry intrusion, and are associated with widespread illite-carbonate (argillic) alteration. Multiphase fluid inclusions in quartz stockwork veins associated with the potassic alteration trapped a highly saline (50-84 wt% NaCl equiv.) magmatic fluid at high temperatures (450 to >600 °C). These hypersaline brines were probably trapped at a pressure of about 300 bar, corresponding to a depth of 1.2 km under lithostatic conditions. This shallow depth is consistent with textures of the host dacite porphyry and reconstruction of the volcanic stratigraphy. Liquid-rich fluid inclusions in the quartz stockwork veins and quartz phenocrysts trapped a lower salinity (3-20 wt% NaCl equiv.), moderate temperature (300-400 °C) fluid that may have caused the phyllic alteration. Fluid inclusions in the quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins trapped dilute (1-3 wt% NaCl equiv.) fluids at 250 to 320 °C, at a minimum depth of 1.0 km under hydrostatic conditions. Oxygen isotopic compositions of the fluids that deposited the quartz stockwork veins fall within the 6 to 10‰ range of magmatic waters, whereas the quartz-sulphide-gold-anhydrite veins have lower '¹⁸O_water values (-0.6 to 0.5‰), reflecting a local meteoric water (-6‰) influence. A '¹⁸O versus 'D plot shows a trend from magmatic water in the quartz stockwork veins to a near meteoric water composition in kaolinite from the advanced argillic alteration. Data points for pyrophyllite and the quartz-sulphide-gold-anhydrite veins lie about midway between the magmatic and meteoric water end-member compositions. The spatial association between porphyry Cu-Mo-Au mineralisation, advanced argillic alteration and quartz-sulphide-gold-anhydrite veins suggests that they are all genetically part of the same hydrothermal system. This is consistent with K-Ar dates of 11.6-10.7 Ma for the intrusive porphyry, for alunite in the advanced argillic alteration, and for sericite selvages from quartz-gold veins in the Thames district.     

黑龙江金厂金矿床18号矿体围岩蚀变及短波红外光谱特征

金厂金矿18号矿体围岩蚀变发育顺序从早到晚为:钾化、硅化、绿泥石化、绢云母化、碳酸盐化、高蛉土化,从内往外依次发育青磐岩化带、绢英岩化带和钾化带.矿化出现在泥化和绢英岩化叠加处,以及泥化和青磐岩化叠加处.通过短波红外光谱测试技术,识别出本矿区有26种蚀交矿物,其中白云母含量与金矿体呈正相关,说明绢云母化与金矿化关系密切;青磐岩化带蚀变矿物组合为绿泥石+绿帘石+伊利石±埃洛石±蒙脱石±石英;钾化带蚀变矿物组合为钾长石+高岭石+埃洛石±蒙脱石±石英;绢英岩化带蚀变矿物组合为绢云母+埃洛石±蒙脱石±高岭石±石英.     

Spectral characteristics of minerals in alteration zones associated with porphyry copper deposits in the middle part of Kerman copper belt,SE Iran

Visible near infrared and shortwave infrared (VNIR-SWIR, 350 to 2500 nm) reflectance spectra obtained from an analytical spectral device (ASD) have been used to define alteration zones adjacent to porphyry copper deposits (PCDs), in the central part of Kerman magmatic arc, SE Iran. The spectral analysis identified sericite, illite, halloysite, montmorillonite, dickite, kaolinite, pyrophyllite, biotite, chlorite, epidote, calcite, jarosite, and iron oxyhydroxides (e.g. hematite, goethite) of hydrothermal and supergene origin. Identified alteration zones are classified into six principal types namely phyllic, phyllic/propylitic, propylitic, potassic, argillic and advanced argillic. The iron oxide minerals in the oxidized zone were also identified using spectral analysis. Results of spectral analyses of samples are consistent with mineralogical data obtained from X-ray diffraction (XRD) and petrographic studies. Spectroscopic studies by ASD demonstrate that this tool is very useful for semi-quantitative and cost effective identification of different types of alteration mineral assemblages. Furthermore, it can provide a valuable tool for evaluating aerial distribution of alteration minerals while coupled with remote sensing data analysis.     

Gold Abundance and Stable Isotopes (H, O, S) in Hydrothermal Alteration Zones of Gasa Island (Gasado), Korea

Geology of the Gasa Island (Gasado), Korea, consists mainly of tuffaceous rocks, rhyolite and andesitic rocks related to Cretaceous volcanic activity. These rocks are hydrothermally altered, and are classified into the following four alteration zones based on the alteration mineral assemblages: advanced argillic alteration (alunite‐pyrophyllite‐kaolinite‐pyrite); sericitic alteration (sericite‐kaolinite‐quartz); propylitic alteration (quartz‐chlorite‐carbonate‐pyrite); and silicified zones. Alunite in the advanced argillic zone occurred in two types; a massive or disseminated type and a vein type. Most of the massive or disseminated alunites are ≥50 μm in size, whereas the size of vein alunites is <20–30 μm. Alunite grain size is greater in the central part of disseminated or massive alunite, while it is smaller toward the margins. The gold content of each alteration zone is 21–2900 ppb, 15–88 ppb, 57–1730 ppb, and 2–231 ppb, respectively. The gold content of quartz veins developed in the alteration zones is 39–715 ppb. Gold is enriched in the minerals and rocks around faults and fissures, and is strongly concentrated in the advanced argillic alteration zone around faults. Hydrothermal solutions traveling along the fracture systems might be responsible for the comparatively high gold content in the study area. δ³⁴S of alunites occurring in the advanced argillic alteration zone range from +16.5 to +3.9‰, although most are in a comparatively narrow range from +8.6 to +5.2‰. There is no difference between disseminated or massive and vein alunites. The δ³⁴S of pyrites in the advanced argillic alteration zone are from +4.8 to ?2.9‰. Oxygen and hydrogen isotope values of alunites are from +8.5 to 0‰ and from ?59.6 to ?97.3‰, respectively. With an assumed temperature of 200°C, δD and δ¹⁸O of hydrothermal solutions calculated for alunites are from ?53.6 to ?91.3‰, and from ?2.4 to ?8.1 for massive or disseminated alunites and from ?6.6 to ?10.9‰ for vein alunites, respectively. These data suggest that meteoric water dominated during the alunite formation. Isotopic data, geological setting, mineralogy, size of alunite and pure alunite composition (K end member) indicate that alunites of the study area were formed in the steam‐heated environment of acid sulfate alteration.     

Enhancement of hydrothermal alteration zones using the spectral feature fitting method in Rabor area, Kerman, Iran

Rabor exploration area is in southeast of Kerman province, south of Urumieh-Dokhtar volcanic belt. Since there are many evidences of porphyry copper mineralization in this belt, prospecting and exploration of the intact and undiscovered places, especially the southern part of this belt, seems necessary. In this paper, use has been made of the “spectral feature fitting” (SFF) method to process ASTER satellite data (in Rabor exploratory area as a case study) for the identification and enhancement of hydrothermal alteration zones related to probable porphyry copper mineralization. The method is based on the comparison of absorption features in the image and the reference spectra. The distribution map of the indicator clay minerals, such as kaolinite, muscovite, illite, montmorillonite, alunite, pyrophyllite, dickite, chlorite, and epidote in Rabor exploratory area has been prepared with the help of this method. Identification and enhancement of alteration zones and overlaying Pay-Negin ore index on every individual zone reveal the capability and high efficiency of the SFF method in processing ASTER satellite data and preparing the distribution map of alteration minerals. Field and laboratory studies have shown that main alterations in this area are phyllic and argillic. These studies confirm the results obtained from remote sensing in the area.     

The Lanthanide Tetrad Effect in Argillic Alteration: An Example from the Jizvan District,Northern Iran

Intrusion of quartz‐monzodioritic igneous bodies of Oligocene age into Eocene lithic crystal tuffs and trachy‐basalts resulted in the occurrence of a widespread argillic alteration zone in the Jizvan district (northern Iran). Mineralogically, the argillic alteration zone includes minerals such as kaolinite, quartz, smectite, pyrophyllite, muscovite‐illite, alunite, rutile, calcite, feldspar, chlorite, hematite and goethite. Therefore, the non‐CHARAC behaviour for trace elements in the argillic samples is reflected in the non‐chondritic Y/Ho and Zr/Hf ratios and the irregular REE patterns, which appear related to the tetrad effect phenomenon. The chondrite‐normalized REE distribution patterns indicate both concave (W‐shaped) and convex (M‐shaped) tetrad effects in the argillic samples. Based on the field evidence and the results from geochemical studies, it can be concluded that the samples from the argillic alteration zone having high fourth tetrad effect values (>0.30) were developed in the fault and breccia zones. The results indicate that factors such as preferential scavenging by Mn‐oxides, crystallization of clay minerals, fluid‐rock interaction, overprint of hypogene mineral assemblage by supergene ones, and the structural control, have all played an important role in the occurrence of tetrad effects in samples of the argillic zone in the Jizvan district.     

合成金刚石生产中叶蜡石传压密封材料矿物学研究

叶蜡石是高温高压合成金刚石的关键辅助材料。叶蜡石传压密封材料的性能主要取决于叶蜡石矿石的矿物组成。叶蜡石矿石中的杂质矿物主要是一水硬铝石、明矾石、长石、高岭石、绢云母、绿泥石、石英、赤铁矿、钛铁矿、褐铁矿、金红石等。具有层状结构的矿物－水硬铝石、高岭石、绢云母、绿泥石等总量不超过10％，不会影响制品的传压性能。明矾石在高温高压下不稳定，是有害组分。长石、石英等非层状结构的矿物含量高时，会使叶蜡石传压密封材料静压流变特性变差，对传压性能是有害组分，应控制在小于5％，非常纯净的叶蜡石矿石制成的粉压块传压性能良好，但内摩擦系数小，密封性能差，常发生高压挤出和顶锤破坏现象，少量的赤铁矿、钛铁矿、褐铁矿、金红石矿物存在可以提高密封性能。     

甘肃岗岔—克莫地区蚀变岩特征与找矿预测

岗岔—克莫金矿区位于西秦岭北缘夏河—合作成矿带,具浅成低温热液型矿床特征,初步显示深部可能具有斑岩成矿系统存在。利用短波红外光谱矿物分析技术对岗岔—克莫金矿区蚀变岩特征的研究表明,矿区内发育的蚀变矿物主要有白云母、伊利石、蒙脱石、高岭石、地开石、绿泥石、绿帘石和次生石英等。近矿蚀变类型主要为绢英岩化。矿区内以下家门沟口为中心向外依次发育了中心带(绢英岩化带)、过渡带(泥化带)和外围带(青磐岩化带)。此外,伊利石结晶度以下家门沟口为中心向外具有明显的降低趋势。研究结果指示下家门沟口可能是矿区的热液活动中心。     

藏东芒康县巴达铜金矿床地质特征及找矿方向研究

巴达铜金矿位于藏东富碱斑岩带南段,是藏东地区近年来新发现的大型铜金矿。虽然对巴达铜金矿开展了大量勘查工作,但对该矿床的成因尚未取得共识。本文基于详细的野外调研、岩心与坑道编录及系统的镜下鉴定,对巴达铜金矿床地质特征进行研究。巴达矿床主要产于石英二长斑岩中,局部产于斑岩和砂岩地层的接触带内。矿床发育的围岩蚀变主要为青磐岩化、钾化、绢英岩化,高岭土化、蛋白石化、蒙脱石化次之,蚀变分带从内向外依次为钾硅酸盐化带、绢英岩化带、青磐岩化带、高岭土化带,铜金矿体主要赋存于钾硅酸盐化和绢英岩化带内,铜矿化主要以黄铜矿形式产出,金矿化主要以银金矿形式产于白云石±石英+细粒黄铁矿±黄铜矿脉中,铜矿化与金矿化呈正相关,矿体的产出受北西向逆冲断层的控制。与典型斑岩和浅成低温热液矿床不同,巴达铜金矿化主要产于白云石±石英+黄铁矿脉中;矿床内既发育碳酸盐、伊利石、绢云母和黄铁矿、黄铜矿、方铅矿、黝铜矿、低FeS闪锌矿等一套中硫型浅成低温热液矿床的蚀变矿物组合,又发育符合碱性斑岩系统的特征矿物赤铁矿。基于以上特征判断,巴达铜金矿矿床成因类型应为与富碱斑岩有关的浅成低温热液矿床,巴达铜金矿矿床成因的厘定,为下一步找矿提供了理论指导。     

Geology and Hydrothermal Alteration of the Duobuza Gold‐Rich Porphyry Copper District in the Bangongco Metallogenetic Belt,Northwestern Tibet

The Duobuza gold‐rich porphyry copper district is located in the Bangongco metallogenetic belt in the Bangongco‐Nujiang suture zone south of the Qiangtang terrane. Two main gold‐rich porphyry copper deposits (Duobuza and Bolong) and an occurrence (135 Line) were discovered in the district. The porphyry‐type mineralization is associated with three Early Cretaceous ore‐bearing granodiorite porphyries at Duobuza, 135 Line and Bolong, and is hosted by volcanic and sedimentary rocks of the Middle Jurassic Yanshiping Formation and intermediate‐acidic volcanic rocks of the Early Cretaceous Meiriqie Group. Simultaneous emplacement and isometric distribution of three ore‐forming porphyries is explained as multi‐centered mineralization generated from the same magma chamber. Intense hydrothermal alteration occurs in the porphyries and at the contact zone with wall rocks. Four main hypogene alteration zones are distinguished at Duobuza. Early‐stage alteration is dominated by potassic alteration with extensive secondary biotite, K‐feldspar and magnetite. The alteration zone includes dense magnetite and quartz‐magnetite veinlets, in which Cu‐Fe‐bearing sulfides are present. Propylitic alteration occurs in the host basic volcanic rocks. Extensive chloritization‐silicification with quartz‐chalcopyrite or quartz‐molybdenite veinlets superimposes on the potassic alteration. Final‐stage argillic alteration overlaps on all the earlier alteration. This alteration stage is characterized by destruction of feldspar to form illite, dickite and kaolinite, with accompanying veinlets of quartz + chalcopyrite + pyrite and quartz + pyrite assemblages. Cu coexists with Au, which indicates their simultaneous precipitation. Mass balance calculations show that ore‐forming elements are strongly enriched during the above‐mentioned three alteration stages.     

Mineralogy,textures, and whole-rock geochemistry of advanced argillic alteration: Hugo Dummett porphyry Cu–Au deposit,Oyu Tolgoi mineral district,Mongolia

Advanced argillic (AA) alteration is developed over a vertical interval of 500 m, above (and enclosing) Late Devonian quartz monzodiorite intrusions that accompany porphyry-style Cu–Au mineralization at the Hugo Dummett deposit. The AA alteration is mainly in basaltic rocks and locally extends into the overlying dacitic ash-flow tuff for about 100 m. The AA zone overprints porphyry-style quartz veins associated with quartz monzodiorite intrusions, but at least partly precedes high-grade porphyry-style bornite mineralization. Mineralogically, it consists of andalusite, corundum, residual quartz, titanium oxides, diaspore, alunite, aluminum phosphate-sulfate (APS) minerals, zunyite, pyrophyllite, topaz, kaolinite, and dickite, as well as anhydrite and gypsum, but is dominated by residual quartz and pyrophyllite. Alteration zonation is not apparent, except for an alunite-bearing zone that occurs approximately at the limit of strong quartz veining. Whole-rock geochemistry shows that the AA alteration removes most major elements except Si, Al, Ti, and P, and removes the trace elements Sc, Cs, and Rb. V, Zr, Hf, Nb, Ta, U, and Th are relatively immobile, whilst light REEs (La to Nd), Sr, Ba, and Ga can be enriched. Middle REEs (Sm to Gd) are moderately depleted; Y and heavy REEs (Tb to Lu) are strongly depleted except in two unusual samples where middle to heavy REEs are enriched.     

Geology and Hydrothermal Alteration of the Milyang Pyrophyllite Deposit, Southeast Korea

Abstract: The Milyang pyrophyllite deposit, which is embedded in the Late Cretaceous Yuchon Group of the Kyongsang Supergroup, is one of the largest hydrothermal clay deposits in the Kyongsang basin, southeast Korea. Host rocks of the deposit are porphyritic andesite lava and minor andesitic lapilli tuff. In the Milyang district, a hydrothermally altered zone is about 2 × 3 km in extent; we can recognize the concentric arrangement of advanced argillic, propylitic, and sericitic alteration zones from the central to peripheral parts of the zone. The Milyang pyrophyllite deposit forms a part of the advanced argillic alteration zone. The Milyang pyrophyllite deposit is subdivided into the following four zones based on mineral assemblages: the pyrophyllite zones 1, 2, 3, and the silicified zone. The pyrophyllite zone 1, which occupies the central part of the deposit, comprises mainly pyrophyllite, kaolinite, and diaspore without quartz. Diaspore nodules often concentrate in beds 40–50 cm thick. Andalusite, dumortierite, and tourmaline locally occur as network veins, crack‐filler, or small spherulitic spots. The Al₂O₃ content of the ore ranges from 27 to 36 wt%. The pyrophyllite zone 2, which constitutes a major part of the deposit, comprises mainly pyrophyllite, kaolinite, and quartz. The Al₂O₃ content of the ore ranges from 15 to 24 wt%. The pyro‐phyllite zone 3 is the hematite‐rich marginal facies of the deposit. The silicified zone, which occurs as beds and septa, is mostly composed of quartz with minor pyrophyllite and kaolinite; the SiO₂ contents range from 79 to 90 wt%. Comparing chemical compositions of the high‐Al ores with those of unaltered host andesite, the Fe, Ca, alkalis, HFSE, and HREE contents are significantly depleted, whereas S, B, As, Sr, and LREE are enriched. The hydrothermal alteration of the Milyang pyrophyllite deposit can be classified into the following four stages: 1) extensive sericitic and propylitic alteration, 2) medium‐temperature (200–250°C) advanced argillic alteration, 3) high‐temperature (250–350°C or more) advanced argillic alteration, and 4) retrograde low‐temperature alteration. The heat and some volatile components such as B and S would be derived from the Pulguksa Granite intruded underneath the deposit.     

Unveiling the hydrothermal mineralogy of the Chapi Chiara gold prospect,Peru, through reflectance spectroscopy,geochemical and petrographic data

Southern Peru contains important epithermal Au–Ag (± base metals) deposits, such as Canahuire, Tucari, Santa Rosa, Caylloma, Shila and Paula. The Chapi Chiara gold prospect is located in this region and is part of a paleo-stratovolcano of the Upper Miocene–Pliocene. The hydrothermal alteration of the prospect was characterized based on spectroradiometric data, geochemistry and petrography. The mineralogical data, interpreted based on reflectance spectroscopy, were spatialized using the sequential indicator simulation technique for producing probabilistic maps of alteration. The inner part of the paleo-stratovolcano (SW sector) is marked by three main cores of advanced argillic alteration (AAA) (quartz–alunite supergroup minerals–kaolinite–dickite ± topaz ± pyrophyllite ± diaspore) associated with topographic highs. The AAA1 core is surrounded by argillic alteration (quartz–illite–paragonitic illite–smectite ± pyrite) and propylitic alteration (quartz–plagioclase–chlorite–calcite–epidote–smectite ± kaolinite ± pyrite ± chalcopyrite ± magnetite). The central sector of the prospect, situated in the NE flank of the paleo-stratovolcano, is characterized by hydrothermal breccias structured towards N65E. The main mineral phases comprise quartz and abundant pyrite, sometimes with traces of As. Anomalous geochemical values of Ag, As, Bi, Hg, Se, Sb and Te coincide with high gold contents in this sector of the prospect. Jarosite and goethite are evidence of a subsequent supergene event. Based on the mineralogical characterization, we conclude the existence of a high sulfidation epithermal system in Chapi Chiara. Hypogene minerals of higher temperature in the SW sector of the prospect, such as diaspore, pyrophyllite and topaz in the AAA zone, and epidote in the propylitic alteration zone, can reveal that the system is currently in a relatively deep erosion level, suggesting its proximity in relation to the interface between a deep epithermal system and a mesothermal system.     

Porphyry to epithermal transition in the Agua Rica polymetallic deposit, Catamarca, Argentina: An integrated petrologic analysis of ore and alteration parageneses

Agua Rica (27°26′S–66°16′O) is a world class Cu–Au–Mo deposit located in Catamarca, Argentina. In the E–W 6969400 section examined, the Seca Norte and the Trampeadero porphyries that have intruded the metasedimentary rock are cut by interfingered igneous and hydrothermal heterolithic and monolithic breccias, and sandy dikes. Relic biotite and K-feldspar of the early potassic alteration (370° to > 550 °C) with Cu (Mo–Au) mineralization are locally preserved and encapsulated in a widespread, white mica + quartz + rutile or anatase halo (phyllic alteration) with pyrite + covellite that suggests fluids with temperatures ≤ 360 °C and high f(S₂). The Trampeadero porphyry and the surrounding metasedimentary rock with phyllic alteration have molybdenite in stringers and B-type quartz veinlets and the highest Mo grades (> 1000 ppm).Multistage advanced argillic alteration overprinted the earlier stages. Early andalusite ± pyrite ± quartz is preserved in the roots of the argillic halo rimmed by an alumina–silica material and white micas. This alteration assemblage is considered to have been formed at temperatures ≥ 375 °C from condensed magmatic vapor. At higher levels, pyrophyllite replaces muscovite and illite in clasts of hydrothermal breccias in the center and east sector of the study section, suggesting temperatures of 280 to 360 °C. Clasts of vuggy silica in the uppermost levels of the central breccia, indicates that at lower temperatures (< 250 °C), fluids reached very low pH (pH < 2). In this early stage of the advanced argillic alteration, hydrothermal fluids seem to have not precipitated sulfides or sulfosalts.Hydrothermal brecciation was concurrent with fluid exsolution (↑? V), which precipitated intermediate-temperature advanced argillic alunite (svanbergite + woodhouseite) ± diaspore ± zunyite as breccia cement along with abundant covellite + pyrite + enargite ± native sulfur ± kuramite at intermediate depths and in lateral transitional zones to unbrecciated rocks. This mineral assemblage indicates temperatures near 300 °C, oxidized and silica-undersaturated hydrothermal fluids with high sulfur fugacity to prevent gold precipitation. Multiple generations of pyrite, emplectite, colusite, Pb- and Bi-bearing sulfosalts, and native sulfur with Au and Ag, accompanied by alunite introduction in the upper level breccias, probably occurred at lower temperatures, but still high sulfur and oxygen activity. An independent Zn and Pb (as galena) mineralization stage locally coincides with Au–Ag and sulfosalts, and advanced at depth, controlled by fractures and overprinting much of the previous mineralization. A later paragenesis of veinlets of alunite + woodhouseite + svanvergite + pyrite ± enargite that cut the phyllic halo suggests temperatures ~ 250 °C and without woodhouseite + svanvergite, temperatures ~ 200 °C. Kaolinite occurs in the phyllic halo as a late mineral in clots and in veinlets thus, in this zone, the fluid had cooled enough for its formation.     

基于红外光谱技术研究云南普朗斑岩铜矿的蚀变和矿化特征

近年来红外光谱技术作为一种绿色、快速、无损、精确探测矿物的技术手段而倍受关注,针对斑岩型矿床蚀变矿物高度叠加、蚀变分带界线不明显、细粒蚀变矿物多、黏土蚀变矿物多等特征,该技术在蚀变矿物识别和勘探信息解读等方面优势突出。本文应用红外光谱技术对云南普朗斑岩铜矿区钻孔ZK1801岩心进行矿物识别和蚀变分带划分的研究,识别出钾硅酸盐化带、绿帘石-绿泥石化带、绿泥石-伊利石化带、石英-伊利石化带和泥化带。研究表明:普朗铜矿整个钻孔的蚀变矿物主要有石英、钾长石、绢云母、绿泥石、绿帘石、高岭石、蒙脱石、伊利石等;根据矿化特征,发现铜矿体广泛赋存在钾硅酸盐化带和绿帘石-绿泥石化带中,与矿化关系密切的蚀变矿物"石英+钾长石+绢云母"和"绿帘石+绿泥石",可以作为普朗矿床勘查的标型蚀变矿物组合;研究区广泛发育的绢云母Al—OH波长随钻孔深度增加而逐渐从2210～2205nm减小到2202～2198nm, Al—OH波长2210～2205nm(长波绢云母)与矿化关系密切,可以作为普朗矿床勘查的指示信息。     

西藏羊八井地热田水热蚀变

本文对羊八井地热田钻扎ZK-201、ZK-301和ZK-308的岩心进行了较系统的蚀变矿物学、岩石学和流体包体研究。划分出6个蚀变矿物共生组合及蚀变分带,讨论了蚀变过程中岩石化学变化的特点,并推测了蚀变的温度和酸碱度条件。研究表明,热田曾处于极度的活动状态,最高温度达220-240℃,由于冷水的入侵,热田在目前钻探所及范围已冷却了50-70℃。蚀变矿物分布模式表明,目前热田流体主通道位于北部,热田进一步的开发应以寻找北部深部高温流体为主。     

碰撞造山型斑岩铜矿蚀变分带模式--以西藏冈底斯斑岩铜矿带为例

岛弧环境斑岩铜矿蚀变分带模式已为人们所熟知 ,但碰撞造山环境的斑岩铜矿蚀变分带特征尚不清楚。对此 ,文中以西藏冈底斯斑岩铜矿带为例 ,选择驱龙、冲江、厅宫 3个典型斑岩铜矿 ,对其蚀变系统进行了系统研究。依据蚀变矿物组合可分为 3个蚀变带 ,呈环带状分布。从中心向外依次为钾硅酸盐化带、石英绢云母化带、青磐岩化带。泥化带不太发育 ,通常叠加在其它蚀变带之上。钾硅酸盐化带主要蚀变矿物为钾长石、黑云母、石英、硬石膏 ,伴有大量的黄铜矿与辉钼矿 ,是成矿物质的主要堆积区。石英绢云母化带与钾硅酸盐化带渐变过渡或叠加其上 ,是次于钾硅酸盐化带的储矿部位。蚀变矿物组合为绢云母 +石英 +钾长石 ,金属硫化物有黄铁矿、黄铜矿、辉钼矿、斑铜矿 ,少量的方铅矿、闪锌矿。主要的辉钼矿以石英 +辉钼矿脉的形式出现于本矿带。青磐岩化在斑岩体内不发育 ,矿化极微弱。蚀变岩石组分分析表明 ,岩石蚀变及其分带是岩浆流体 /岩石反应时K ,Na ,Ca ,Mg等组分迁移的结果 ,矿化伴随着蚀变发生。钾硅酸盐化带、石英绢云母化带和青磐岩化带的蚀变岩石与未 (弱 )蚀变斑岩具有一致的稀土配分模式 ,REE含量有规律地变化 ,说明蚀变岩石均经历了源于岩浆的流体的交代 ,不同的蚀变形成于岩浆流体演化的不同阶段。蚀?     

Mg–Fe carpholites from aluminous schists in the Diahot region and implications for preservation of high-pressure/low-temperature schists, northern New Caledonia

Abstract Mg–Fe carpholite is widespread in the Diahot region of New Caledonia in highly aluminous schists and as veins in what was originally a clay-rich hydrothermal alteration envelope about massive suphide deposits. These carpholites have Fe/(Fe + Mg) ratios of 0.03–0.65 and no significant Mn component. Mg-carpholite + quartz occur in assemblages with chlorite or pyrophyllite, pyrophyllite + kaolinite and pyrophyllite + diaspore. Temperatures of 230–320° C and minimum pressures of 7 kbar are indicated for the Mg–Fe carpholite-bearing rocks. The regional distribution of aragonite and Mg–Fe carpholite parallel to a major zone of dominantly transcurrent movement and oblique to the trend of the subduction complex indicates the high- P /low- T schists owe their rapid uplift and preservation to the vertical component of the transcurrent faulting.     

Hydrothermal Alteration of the Saplica Volcanic Rocks,Sebinkarahisar, Turkey

A widespread, intense hydrothermal alteration zone has developed in the Cretaceous Saplica volcanics as a result of the intrusion of Late Cretaceous-Paleocene granitoids. The propylitic, phyllitic (sericitic), and argillic alteration along with hematite, silica polymorphs, and two types of tourmaline mineralization developed under a wide range of Eh and pH conditions.

Alunite, kaolinite, and silica are abundant in the argillic alteration, whereas sericite dominates in the phyllic alteration. Most of the major alunite deposits are located along the periphery of the Saplica volcanic rocks and in addition contain alunite, kaolinite + quartz ± opal ± cristobalite. Illite and pyrite, barite, and gypsum also occur in small amounts.

Major and trace elements are concentrated in, or were leached from, the volcanic rocks, depending upon the alteration types. In general, Al + K and Mg + Ca + Fe were enriched in the alunitic + sericitic and propylitic alteration types, respectively. On the other hand, Ca, Mg, and Fe were leached during argillic alteration, and Fe was concentrated in hematite formation. Strong leaching of Na was determined for alteration types. Silica generally decreased in argillitic (kaolinitic and alunitic) alteration zones. Most trace elements were mobile during hydrothermal alteration. Y, Sc, Mo, Cr, Co, Ni, and Zn tend to be mobile in acid aqueous systems, and thus are nearly absent in these alunitic alteration zones. In the surrounding kaolinitic envelope, these elements are present at background (average) or slightly higher concentrations. Rb and Sr contents are high in the alunitic and kaolinitic zones. Barium is highest near the alunite zone because of the relative insolubility of barite in acidic solutions. Pb and Cu contents increase in the propylitic zone. Such hydrothermal alteration zones can be used effectively in the exploration and evaluation of mineral resources of the eastern Black Sea region.     

Geochemistry and alteration facies associated with epithermal precious metal mineralization in an active geothermal system,northern Lesbos,Greece

Hydrothermal quartz veins associated with gold and silver mineralization and variable amounts of base metal sulfides have been discovered within an active geothermal system in the Megala Therma area of northern Lesbos. This geothermal system is probably a late evolutionary stage in the formation of this mineralization. The veins are hosted in Upper Miocene volcanic rocks of andesitic composition and consist of quartz, adularia, chlorite, sericite, illite, kaolinite, baryte, small amounts of jarosite and alunite, and native gold, pyrite, galena, sphalerite, chalcopyrite, bornite, chalcocite, covellite and goethite. The principal types of alteration which occur in the studied area are: silicification, propylitization, argillic alteration and potassic, phyllic alteration.