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1.
This report presents mineralogical, geochemical and isotopic data on samples obtained using the Benthic Multi‐coring System (BMS) to drill a submarine hydrothermal deposit developed in a caldera on the summit of the Suiyo Seamount in the Izu–Bonin Island Arc, south of Japan. This deposit is regarded as the first example of Kuroko‐type sulfide mineralization on a volcano at the volcanic front of an island arc. The mineralization and hydrothermal alteration below the 300 × 150‐m area of active venting was investigated to depths of 2–9 m below the sea floor. Drilling beneath the area of active venting recovered a sequence of altered volcanic rocks (dacite lavas, pyroclastic rocks of dacite–rhyolite compositions and pumice) associated with sulfide veining and patches/veins of anhydrite. No massive sulfide was found, however, and the subsea‐floor mineralization to 10 m depth is dominated by anhydrite and clay minerals with some sulfides. Sulfide‐bearing samples contained high Au (up to 42 ppm), Ag (up to 263 ppm), As (up to 1550 ppm), Hg (up to 55 ppm), Sb (up to 772 ppm), and Se (up to 24 ppm). Electron probe microanalyzer indicated that realgar, orpiment, and mimetite were major As‐bearing minerals. The sulfides were also characterized by high Zn (>10%) compared to Cu (<6.3%) and Pb (<0.6%). The δ202Hg/198Hg, δ202Hg/199Hg and δ202Hg/200Hg of the sulfide‐bearing dacite samples and a sulfide chimney decreased with increasing Hg/Zn concentration ratio. The variation of the δ202Hg/198Hg ranged from ?2.8 to +0.5‰ to relative to S‐HG02027. The large range of these δ202Hg/198Hg was greater than might be expected for such a heavy element and may be due to a predominance of kinetic effects. The variation of δ202Hg/198Hg of sulfide‐bearing dacite samples suggested that light Hg isotope in the vapor mixed with oxygenated seawater near sea floor during mineralization. Lead isotope ratios of the sulfide were very similar to those of the dacite lava, suggesting that lead is of magmatic origin. The 87Sr/86Sr ratio (0.70872) of anhydrite was different from that of the dacite lava, and suggests an Sr derivation predominantly from seawater. Hydrothermal alteration of the dacite in the Suiyo hydrothermal field was characterized by Fe‐sulfides, anhydrite, barite, montmorillonite, chlorite/montmorillonite mixed‐layer minerals, mica, and chlorite with little or no feldspar or cristobalite. Hydrothermal clay minerals changed with depth from montmorillonite to chlorite/montmorillonite mixed‐layer minerals to chlorite and mica. Hydrogen isotope ratios of chlorite/montmorillonite and mixed‐layer, mica‐chlorite composites obtained below the active venting sites ranged from ?49 to ?24‰, suggesting seawater as the dominant fluid causing alteration. Oxygen isotope ratios of anhydrite ranged from 9.2 to 10.4‰ and anhydrite formation temperatures were calculated to be 188–207°C. Oxygen isotope ratios ranged from +5.2 to +9.2‰ for montmorillonite, +3.2 to +4.5‰ for chlorite/montmorillonite mixed‐layer minerals, and +2.8 to +3.8‰ in mixtures of chlorite and mica. The formation temperatures of montmorillonite and of the chlorite–mica mixture were 160–250°C and 230–270°C, respectively. The isotope temperatures for clay minerals (220–270°C) and anhydrite (188°C) were significantly lower than the borehole temperature (308.3°C) measured just after the drilling, suggesting that temperature at this site is now higher than when clay minerals and anhydrite were formed.  相似文献   

2.
The Yonaguni Knoll IV hydrothermal vent field (24°51′N, 122°42′E) is located at water depths of 1370–1385 m near the western edge of the southern Okinawa Trough. During the YK03–05 and YK04–05 expeditions using the submersible Shinkai 6500, both hydrothermal precipitates (sulfide/sulfate/carbonate) and high temperature fluids (Tmax = 328°C) presently venting from chimney‐mound structures were extensively sampled. The collected venting fluids had a wide range of chemistry (Cl concentration 376–635 mmol kg?1), which is considered as evidence for sub‐seafloor phase separation. While the Cl‐enriched smoky black fluids were venting from two adjacent chimney‐mound structures in the hydrothermal center, the clear transparent fluids sometimes containing CO2 droplet were found in the peripheral area of the field. This distribution pattern could be explained by migration of the vapor‐rich hydrothermal fluid within a porous sediment layer after the sub‐seafloor phase separation. The collected hydrothermal precipitates demonstrated a diverse range of mineralization, which can be classified into five groups: (i) anhydrite‐rich chimneys, immature precipitates including sulfide disseminations in anhydrite; (ii) massive Zn‐Pb‐Cu sulfides, consisting of sphalerite, wurtzite, galena, chalcopyrite, pyrite, and marcasite; (iii) Ba‐As chimneys, composed of barite with sulfide disseminations, sometimes associated with realgar and orpiment overgrowth; (iv) Mn‐rich chimneys, consisting of carbonates (calcite and magnesite) and sulfides (sphalerite, galena, chalcopyrite, alabandite, and minor amount of tennantite and enargite); and (v) pavement, silicified sediment including abundant native sulfur or barite. Sulfide/sulfate mineralization (groups i–iii) was found in the chimney–mound structure associated with vapor‐loss (Cl‐enriched) fluid venting. In contrast, the sulfide/carbonate mineralization (group iv) was specifically found in the chimneys where vapor‐rich (Cl‐depleted) fluid venting is expected, and the pavement (group v) was associated with diffusive venting from the seafloor sediment. This correspondence strongly suggests that the subseafloor phase separation plays an important role in the diverse range of mineralization in the Yonaguni IV field. The observed sulfide mineral assemblage was consistent with the sulfur fugacity calculated from the FeS content in sphalerite/wurtzite and the fluid temperature for each site, which suggests that the shift of the sulfur fugacity due to participation of volatile species during phase separation is an important factor to induce diverse mineralization. In contrast, carbonate mineralization is attributed to the significant mixing of vapor‐rich hydrothermal fluid and seawater. A submarine hydrothermal system within a back‐arc basin in the continental margin may be considered as developed in a geologic setting favorable to a diverse range of mineralization, where relatively shallow water depth induces sub‐seafloor phase separation of hydrothermal fluid, and sediment accumulation could enhance migration of the vapor‐rich hydrothermal fluid.  相似文献   

3.
The Obiro deposit is located in the Tagawa Acidic Rocks (AR), Uetsu region, NE Japan. The Tagawa AR is composed of a volcanic phase of dacitic welded tuff and a plutonic phase of porphyritic granodiorite. Drill core and ore samples were collected from the deposit and examined by XRD, EPMA, and microthermometry. The drill core samples have suffered pervasively from sericite (illite) alteration, whereas pinkish K‐feldspar alteration halo occur close to veins. The results of EPMA and microthermometry is interpreted as that the magnatic‐hydrothermal fluids has changed as follows; the granodioritic magma intruded at about 1.0 kb and 700°C near the water‐saturated granite solidus; after cooling to about 500°C the fluids boiled according to a change in the pressure regime from lithostatic to hydrostatic; mixing with meteoric water led to sulfide mineralization at around 400°C or less. The main reasons for the mineralization in the Obiro deposit are as follows; the oxidized magma intruded at a shallower level, and thereafter hydrothermal fluids were boiled, resulting in a saline fluid. The saline fluid then dissolved metals such as Pb, Zn, Cu, and Bi, and these metals precipitated during cooling accompanied by dilution of the meteoric water and increasing pH, resulting in decreasing solubility.  相似文献   

4.
Hydrothermal alteration of a quartz‐K‐feldspar rock is simulated numerically by coupling fluid flow and chemical reactions. Introduction of CO2 gas generates an acidic fluid and produces secondary quartz, muscovite and/or pyrophyllite at constant temperature and pressure of 300°C and 200 MPa. The precipitation and/or dissolution of the secondary minerals is controlled by either mass‐action relations or rate laws. In our simulations the mass of the primary elements are conserved and the mass‐balance equations are solved sequentially using an implicit scheme in a finite‐element code. The pore‐fluid velocity is assumed to be constant. The change of rock volume due to the dissolution or precipitation of the minerals, which is directly related to their molar volume, is taken into account. Feedback into the rock porosity and the reaction rates is included in the model. The model produces zones of pyrophyllite quartz and muscovite due to the dissolution of K‐feldspar. Our model simulates, in a simplified way, the acid‐induced alteration assemblages observed in various guises in many significant mineral deposits. The particular aluminosilicate minerals produced in these experiments are associated with the gold deposits of the Witwatersrand Basin.  相似文献   

5.
Acid alteration areas accompanying Quaternary volcanoes are widespread in the western Izu Peninsula, central Japan. The Ugusu alteration area is the largest among them and is mined for “silica stone” at the silica body in the core of the alteration area. Silica zone defined by previous studies is subdivided into highly leached brecciated silica zone and residual silica zone, which extend along a NNW‐SSE–NNE‐SSW direction of fractures/faults. Fe‐rich, alunite, advanced argillic alteration, and intermediate argillic alteration zones occur toward the outside surrounding the two silica zones. The ascent of acid hydrothermal fluid would be responsible for the silica zones and surrounding alteration zones at an earlier stage, while the hydrothermal brecciation and silica veins were caused by a limited supply of silica‐saturated fluids at later stages. Based on the available mineral stability relations and fluid inclusion thermometries, the formation temperatures are estimated to be: >300°C for the residual silica zone; >290°C for the diaspore association in the advanced argillic alteration zone; and <260°C for the kaolinite association in the intermediate argillic alteration zone. The later stage quartz druses have been formed at 200–260°C. The Ugusu–Fukata acid hydrothermal systems were active at 1.5–1.2 Ma, which were temporally related to the Tanaba Andesite volcanism. Hydrothermal system at the Seikoshi gold–silver deposit survived until 0.7 Ma after the volcanism. In the western half of the Izu Peninsula, subduction of the Philippine Sea plate underneath the Suruga Trough caused nearly N–S‐trending maximum horizontal compressive stress (σHmax) and the resultant formation of similarly trending alteration areas and Au‐Ag vein‐type deposits in the Ugusu‐Toi‐Seikoshi area. From a practical viewpoint, at the Ugusu silica stone deposit, the fracture‐controlled vertical morphology of the silica body provides an important guide for exploration. Because the alteration zones occur both in the lower and upper sides of the silica bodies, it is important to make sure to which side the alteration zones correspond.  相似文献   

6.
The common serpentine–diopside matrix assemblage in volcaniclastic kimberlite (VK) at the Venetia Mine, South Africa is ascribed to a secondary origin, because of post‐emplacement serpentinization and associated hydrothermal metamorphism. Volcaniclastic deposits with 20–30% porosity infill kimberlite pipes in the waning stages of kimberlite eruptions. Olivine macrocrysts are typically rimmed by talc and are pseudomorphed by lizardite, with minor magnetite. The fine matrix consists of mixtures of lizardite, chlorite, smectite, brucite, calcite, titanite and andradite, an assemblage which either pseudomorphed microcrysts or in‐filled voids. Locally we recognize microcryst pseudomorphs rich in sub‐microscopic mixtures of lizardite with smectite, and other microcryst pseudomorphs and void‐filling matrix rich in chlorite and lizardite. Interstitial lizardite and associated phyllosilicates (brucite, smectite and chlorite) crystallized progressively from meteoric or hydrothermally derived pore waters, and Si4+ and Mg2+ released into the fluid phase during serpentinization of olivine macrocrysts. Radial‐fibrous fringes of diopside microlites around crystals display void‐filling textures because of unrestricted growth into pore spaces. Secondary diopside is attributed to Si4+, Mg2+ and Ca2+ cations released into the fluid phase by interaction with olivine, calcite and plagioclase in siliceous xenoliths. The paucity of primary, fine‐grained groundmass phases resistant to alteration, for example, perovskite and spinel, precludes an origin for the intergrain matrix as altered interstitial ash, glass or a late‐stage kimberlite melt. Isovolumetric replacement of olivine results in a volume increase of 60% so that pore spaces in the original deposit can be easily filled up with serpentine. The source of Al3+ to form chlorite and smectite is attributed to alteration of plagioclase in xenoliths which comprise 20–30 vol.% of the deposit. Titanite, hydro‐andradite and second‐generation diopside precipitate as hydrothermal minerals from calcium‐bearing serpentinizing fluids in replacement reactions and as void‐filling minerals. Consideration of mineral equilibria in the CaO‐MgO‐SiO2‐H2O‐CO2 system constrains the common matrix assemblage of lizardite and diopside in XCO2)–T space. At 300 bar, the assemblage is stable only at temperatures below 370 °C and XCO2 < 0.01. This upper limit on temperature is well below the plausible solidus of ultrabasic magmas. Furthermore, the requirement of trace CO2 in the fluid phase implies a post‐emplacement external source rather than ‘autometamorphism’ from kimberlite‐derived fluids, because of high PCO2 commonly inferred for kimberlite magmas.  相似文献   

7.
The availability of fluids and drill cuttings from the active hydrothermal system at Roosevelt Hot Springs allows a quantitative comparison between the observed and predicted alteration mineralogy, calculated from fluid-mineral equilibria relationships. Comparison of all wells and springs in the thermal area indicates a common reservoir source, and geothermometer calculations predict its temperature to be higher (288°C ± 10°) than the maximum measured temperature of 268°C.The composition of the deep reservoir fluid was estimated from surface well samples, allowing for steam loss, gas release, mineral precipitation and ground-water mixing in the well bore. This deep fluid is sodium chloride in character, with approximately 9700 ppm dissolved solids, a pH of 6.0, and gas partial pressures of O2 ranging from 10?32 to 10?35 atm, CO2 of 11 atm, H2S of 0.020 atm and CH4 of 0.001 atm.Comparison of the alteration mineralogy from producing and nonproducing wells allowed delineation of an alteration pattern characteristic of the reservoir rock. Theoretical alteration mineral assemblages in equilibrium with the deep reservoir fluid, between 150° and 300°C, in the system Na2O-K2O-CaO-MgO-FeO-Fe2O3-Al2O3-H4SiO4-H2O-H2S-CO2-HCl, were calculated. Minerals theoretically in equilibrium with the calculated reservoir fluid at >240°C include sericite, K-feldspar, quartz, chalcedony, hematite, magnetite and pyrite. This assemblage corresponds with observed higher-temperature (>210°C) alteration assemblage in the deeper parts of the producing wells. The presence of montmorillonite and mixed-layer clays with the above assemblage observed at temperatures <210°C corresponds with minerals predicted to be in equilibrium with the fluid below 240°C.Alteration minerals present in the reservoir rock that do not exhibit equilibrium with respect to the reservoir fluid include epidote, anhydrite, calcite and chlorite. These may be products of an earlier hydrothermal event, or processes such as boiling and mixing, or a result of errors in the equilibrium calculations as a result of inadequate thermochemical data.  相似文献   

8.
Middle Miocene (11.18–10.65 Ma) low sulfidation‐type epithermal gold mineralization occurred in the Cibaliung area, southwestern part of Java Island, Indonesia. It is hosted by andesitic to basaltic andesitic lavas of the Middle Miocene Honje Formation (11.4 Ma) and is covered by Pliocene Cibaliung tuff (4.9 Ma). The exploration estimates mineral resource of approximately 1.3 million tonnes at 10.42 g/t gold and 60.7 g/t silver at a 3 g/t Au cut‐off. This equates to approximately 435,000 ounces of gold and 2.54 million ounces of silver. That resource resulted from two ore shoots: Cibitung and Cikoneng. Studies on ore mineralogy, hydrothermal alteration, geology, fluid inclusion, stable isotopes and age dating were conducted in order to characterize the deposit and to understand a possible mechanism of preservation of the deposit. The ore mineral assemblage of the deposit consists of electrum, naumannite, Ag‐Se‐Te sulfide minerals, chalcopyrite, pyrite, sphalerite and galena. Those ore minerals occur in quartz veins showing colloform–crustiform texture. They are enveloped by mixed layer clay illite/smectite zone, which grades into smectite zone outward. The temperature of mineralization revealed by fluid inclusion study on quartz in the veins ranges from 170 and 220°C at shallow and deep level, respectively. The temperature range is in agreement with the temperature deduced from the hydrothermal alteration mineral assemblage including mixed layered illite/smectite and laumontite. The mineralizing fluid is dilute, with a salinity <1 wt% NaCl equivalent and has stable isotopes of oxygen and hydrogen composition indicating a meteoric water origin. Although the deposit is old enough that it would have been eroded in a tropical island arc setting, the coverage by younger volcanic deposits such as the Citeluk tuff and the Cibaliung tuff most probably prevented this erosion.  相似文献   

9.
Hydrothermal mineral assemblages and related hydrothermally enhanced fracturing are common in the Precambrian Dengying Formation of Central Sichuan Basin. Petrographic and geochemical analyses of core samples show that the hydrothermal dolomite reservoirs of Dengying Formation consist of four main types of pores in the reservoir facies. These include: 1) hydrothermal dissolution vug(or pore), 2) intercrystalline pore, 3) residual inter-breccia vug(or pore), and 4) enlarged dissolved-fracture. There are three different fabrics dolomite in hydrothermal dolomite reservoirs, namely, saddle dolomite, fine-medium dolomite and micritic dolomite. Micritic dolomite is the original lithology of host rock. Saddle dolomite with curved or irregular crystal faces was directly crystallized from hydrothermal fluids(average temperature 192°C). Fine-medium dolomites are the products of recrystallization of micritic dolomite, resulting in abnormal geochemical characteristics, such as slight depletion of δ18O, significant enrichment of Mn-Fe and 87Sr/86Sr, and positive Eu anomaly. A model for the distribution of various hydrothermal dolomite reservoir facies is proposed here, which incorporates three fundamental geological controls: 1) extensional tectonics and tectono-hydrothermal events(i.e., the Xingkai Taphrogenesis of Late Sinian-Early Cambrian, and Emei Taphrogenesis of Late Permian), 2) hydrothermal fluid storage in clastic rocks with large thickness(e.g., Nanhua System of Chengjiang Formation and part of Doushantuo Formation), and 3) confining bed for hydrothermal fluids(such as, the shale in Qiongzhusi Formation). The supply of hydrothermal fluid is critical. Large basement-rooted faults and associated grid-like fracture system may function as the channels for upward migration of hydrothermal fluid flow. The intersection of the above-mentioned faults(including the conversion fault), especially transtensional sags above negative flower structures on wrench faults can serve as a key target for future hydrocarbon exploration.  相似文献   

10.
Talc, kerolite–smectite, smectite, chlorite–smectite and chlorite samples from sediments, chimneys and massive sulfides from six seafloor hydrothermal areas have been analyzed for mineralogy, chemistry and oxygen isotopes. Samples are from both peridotite- and basalt-hosted hydrothermal systems, and basaltic systems include sediment-free and sediment-covered sites. Mg-phyllosilicates at seafloor hydrothermal sites have previously been described as talc, stevensite or saponite. In contrast, new data show tri-octahedral Mg-phyllosilicates ranging from pure talc and Fe-rich talc, through kerolite-rich kerolite–smectite to smectite-rich kerolite–smectite and tri-octahedral smectite. The most common occurrence is mixed-layer kerolite–smectite, which shows an almost complete interstratification series with 5 to 85% smectitic layers. The smectite interstratified with kerolite is mostly tri-octahedral. The degree of crystal perfection of the clay sequence decreases generally from talc to kerolite–smectite with lower crystalline perfection as the proportion of smectite layers in kerolite–smectite increases.Our studies do not support any dependence of the precipitated minerals on the type/subtype of hydrothermal system. Oxygen isotope geothermometry demonstrates that talc and kerolite–smectite precipitated in chimneys, massive sulfide mounds, at the sediment surface and in open cracks in the sediment near seafloor are high-temperature (> 250 °C) phases that are most probably the result of focused fluid discharge. The other end-member of this tri-octahedral Mg-phyllosilicate sequence, smectite, is a moderate-temperature (200–250 °C) phase forming deep within the sediment (～ 0.8 m). Chlorite and chlorite–smectite, which constitute the alteration sediment matrix around the hydrothermal mounds, are lower-temperature (150–200 °C) phases produced by diffuse fluid discharge through the sediment around the hydrothermal conduits. In addition to temperature, other two controls on the precipitation of this sequence are the silica activity and Mg/Al ratio (i.e. the degree of mixing of seawater with hydrothermal fluid). Higher silica activity favors the formation of talc relative to tri-octahedral smectite. Vent structures and sedimentary cover preclude complete mixing of hydrothermal fluid and ambient seawater, resulting in lower Mg/Al ratios in the interior parts of the chimneys and deeper in the sediment which leads to the precipitation of phyllosilicates with lower Mg contents. Talc and kerolite–smectite have very low trace- and rare earth element contents. Some exhibit a negative or flat Eu anomaly, which suggests Eu depletion in the original hydrothermal fluid. Such Eu depletion could be caused by precipitation of anhydrite or barite (sinks for Eu2+) deeper in the system. REE abundances and distribution patterns indicate that chlorite and chlorite–smectite are hydrothermal alteration products of the background turbiditic sediment.  相似文献   

11.
In order to investigate whether geochemical, physiographic and lithological differences in two end‐member sedimentary settings could evoke varied microbe–sediment interactions, two 25 cm long sediment cores from contrasting regions in the Central Indian Basin have been examined. Site TVBC 26 in the northern siliceous realm (10°S, 75·5°E) is organic‐C rich with 0·3 ± 0·09% total organic carbon. Site TVBC 08 in the southern pelagic red clay realm (16°S, 75·5°E), located on the flank of a seamount in a mid‐plate volcanic area with hydrothermal alterations of recent origin, is organic‐C poor (0·1 ± 0·07%). Significantly higher bacterial viability under anaerobic conditions, generally lower microbial carbon uptake and higher numbers of aerobic sulphur oxidizers at the mottled zones, characterize core TVBC 26. In the carbon‐poor environment of core TVBC 08, a doubling of the 14C uptake, a 250 times increase in the number of autotrophic nitrifiers, a four‐fold lowering in the number of aerobic sulphur oxidizers and a higher order of denitrifiers exists when compared with core TVBC 26; this suggests the prevalence of a potentially autotrophic microbial community in core TVBC 08 in response to hydrothermal activity. Microbial activity at the northern TVBC 26 is predominantly heterotrophic with enhanced chemosynthetic activity restricted to tan‐green mottled zones. The southern TVBC 08 is autotrophic with increased heterotrophic activity in the deepest layers. Notably, the bacterial activity is generally dependent on the surface productivity in TVBC 26, the carbon‐rich core, and mostly independent in TVBC 08, the carbon‐poor, hydrothermally influenced core. The northern sediment is more organic sink‐controlled and the southern sediment is more hydrothermal source‐controlled. Hydrothermal activity and associated rock alteration processes may be more relevant than organic matter delivery in these deep‐sea sediments. Thus, this study highlights the relative importance of hydrothermal activity versus organic delivery in evoking different microbial responses in the Central Indian Basin sediments.  相似文献   

12.
At the inside corner between the South Mid‐Atlantic Ridge (SMAR) and the Cardno fracture zone, the 14°S hydrothermal field, with its abundant silica‐rich sulfides, was identified as a volcanic massif, which provided the first opportunity to study inside corner‐related hydrothermal mineralization. S, Pb, and O isotopes were measured in hydrothermal sulfide samples from the two sites (volcanic top and slope sites) in the 14°S field. The homogeneous Pb isotope values (207Pb/204Pb = 15.466 ? 15.472; 206Pb/204Pb = 18.242 ? 18.252) and the δ34S values (top site, +6.3 to +6.85‰; slope site, +2.37 to +3.36‰) suggest that the source of metals and most of the sulfur is the upper crust, whereas some sulfur is sourced from downward‐penetrating seawater, especially in the top site. The calculated oxygen isotope equilibration temperatures from quartz and seawater are between 94 and 144°C for the top site and between 179 and 196°C for the slope site. These isotopic proxies, together with geological background survey data, have an important implication: Discrepancies between the sites may result from variations in crust permeability, which also affect the mixing level between downward‐penetrating seawater and upward hydrothermal end‐member fluids and determine the various mineralization types.  相似文献   

13.
Localized (domainal) low-temperature alteration may indicate variations in the chemistry of alteration fluids and/or discrete fluid flow paths during metamorphism. Occurrences of epidote- and pumpellyite-dominated domains are often used as evidence for large fluxes of Ca-rich fluids. However, comparative studies of two domainal alteration styles from basaltic to andesitic lavas and volcaniclastic rocks at Builth Wells, Wales, UK suggest that such interpretations cannot be applied universally. Here, only one set of domains can be attributed to large fluxes of Ca-rich fluids. In contrast, the second set of domains formed where the host rock supplied the necessary Ca, and fluid/rock ratios were relatively low. These domains are hosted by rocks which show a Caledonian regional metamorphic imprint, characterized by the alteration assemblage albite+chlorite+titanite±prehnite±pumpellyite±calcite±muscovite±quartz (considered to have formed at c. 200°C and ≤2.5 kbar). Type 1 domains lie along fluid channelways, such as veins. Pumpellyite is the dominant secondary mineral, but the alteration assemblage is variable with pumpellyite±prehnite±calcite±titanite±chlorite (±quartz). The domains formed at temperatures of 130–230°C during Ordovician hydrothermal activity, before the peak of regional metamorphism. In contrast, Type 2 domains are not associated with obvious fluid channelways. A central prehnite-dominated zone typically has a rim with the assemblage pumpellyite+calcite±prehnite±chlorite±titanite±K-rich phyllosilicate. These domains probably formed from pelitic xenoliths which contained a volcaniclastic component at temperatures of 130–230°C and at relatively low fluid/rock ratios. However, the timing of domain formation is uncertain. Pyrobitumen, in veins and disseminated throughout the rock, may have influenced the formation of both types of domain by stabilizing pumpellyite in preference to epidote and causing metamorphic calcite formation through the release of CO2 to the alteration fluids. © 1996 John Wiley & Sons, Ltd.  相似文献   

14.
Amphibole is a rock-forming mineral widely existing on the earth. It is easily dissolved and altered during the later stage of diagenesis and mineralization, and often forms chloritization, which is an important indicator for prospecting. To explore amphibole's dissolution process and alteration mechanism, dissolution experiments were carried out under acidic conditions using pargasite-rich amphibole as raw material, and the effects of temperature, p H, and experiment duration on amphibole alteration were investigated. Experimental samples and products were analyzed using X-ray diffractometer, field emission scanning electron microscope, electron probe micro analyzer, and transmission electron microscopy. It was found that many pores and erosion edges are produced after amphibole dissolution, and there is a clear interface between the dissolved residual portion and the parent. The dissolved residual portion remains in the amphibole phase, but as the temperature and time increase, the intensity of the diffraction peak of the phase in the product decreases, and the peak position shifts to a small angle. Many clay minerals such as chlorite and griffithite formed on the amphibole surface. In an environment with strong acidity(p H=3), the amount of chamosite increases with temperature(180°C→210°C→240°C), whereas clinochlore is only increased in a 150–210°C environment. Griffithite growth was observed in the acidic(p H=6) and low temperature(180°C) environments. Based on this analysis, large radius Cl– enters the amphibole lattice or cracks to promote dissolution. The Al-poor and Ca-and Fe-rich regions between the edge and core of the amphibole are caused by dynamic equilibrium in amphibole dissolution and alteration process, which is an essential indicator for the beginning of amphibole dissolution-alteration. Diffusion and the coupled dissolution-reprecipitation mechanism accomplishes the process of dissolution and alteration to form clay minerals. The energy of the system determined by temperature and p H is the key to controlling the rate of growth and nucleation of clay minerals. High temperature and strong acidity will dissolve more iron from amphibole, which is conducive to chlorite growth. Compared to chlorite, griffithite is more sensitive to temperature. Griffithite attaches on the amphibole surface with a star-like in a weak acid and low-temperature environment. The results of this study can provide a mineralogical basis for the analysis of hydrothermal alteration processes and the division of alteration zones.  相似文献   

15.
The Miocene Qulong porphyry Cu‐Mo deposit, which is located at the Gangdese orogenic belt of Southern Tibet, is the largest porphyry‐type deposit in China, with confirmed Cu ～10 Mt and Mo ～0.5 Mt. It is spatially and temporally associated with multiphase granitic intrusions, which is accompanied by large‐scale hydrothermal alteration and mineralization zones, including abundant hydrothermal anhydrite. In addition to hydrothermal anhydrite, magmatic anhydrite is present as inclusions in plagioclase, interstitial minerals between plagioclase and quartz, and phenocrysts in unaltered granodiorite porphyry, usually in association with clusters of sulfur‐rich apatite in the Qulong deposit. These observations indicate that the Qulong magma‐hydrothermal system was highly oxidized and sulfur‐rich. Three main types of fluid inclusions are observed in the quartz phenocrysts and veins in the porphyry: (i) liquid‐rich; (ii) polyphase high‐salinity; and (iii) vapor‐rich inclusions. Homogenization temperatures and salinities of all type inclusions decrease from the quartz phenocrysts in the porphyry to hydrothermal veins (A, B, D veins). Microthermometric study suggests copper‐bearing sulfides precipitated at about 320–400°C in A and B veins. Fluid boiling is assumed for the early stage of mineralization, and these fluids may have been trapped at about 35–60 Mpa at 460–510°C and 28–42 Mpa at 400–450°C, corresponding to trapping depths of 1.4–2.4 km and 1.1–1.7 km, respectively.  相似文献   

16.
G. P. Glasby  K. Notsu   《Ore Geology Reviews》2003,23(3-4):299-339
The Okinawa Trough is a heavily sedimented, rifted back-arc basin formed in an intracontinental rift zone. Submarine hydrothermal activity is located within the six back-arc rifts located in the middle and southern Okinawa Trough and its distribution is controlled principally by tectonic factors. Subduction of the Daito and Gagua Ridges beneath the Ryukyu Arc has resulted in fracturing of the brittle lithosphere beneath the Okinawa Trough. Hydrothermal activity is strongest in the volcanic arc-rift migration phenomenon (VAMP) area plus the JADE site and Southernmost Part of the Okinawa Trough (SPOT) area which form the prolongation of these two ridges. These areas are characterized by extremely high heat flow locally. Submarine hydrothermal fluids from the Okinawa Trough tend to be strongly influenced by interaction of the hydrothermal fluids with organic matter in the sediment resulting in high alkalinity and NH4+ concentrations of the fluids. The fluids also contain high concentrations of CO2 of magmatic origin. Submarine hydrothermal mineralization in the trough is diverse. The CLAM site consists principally of carbonate chimneys. Interaction of the hydrothermal fluid with organic matter in the sediment is particularly strong at this site. This is most probably a sediment-hosted deposit in which sulphide minerals have deposited within the sediment column leaving ‘spent ore-fluids’ to emerge at the seafloor. The JADE site consists of active and inactive sulphide–sulphate chimneys and mounds. The Zn–Pb-rich sulphides at this site contain the highest concentrations of Pb, Ag and Au so far recorded in submarine hydrothermal sulphide deposits. At Minami-Ensei Knoll and Hatoma Knoll, active and inactive chimneys consist principally of anhydrite and barite as a result of phase separation of the hydrothermal fluids beneath the seafloor. An intense black smoker has recently been discovered at Yonaguni Knoll in the SPOT area. If it is confirmed that sulphide mineralization is dominant at this site, this could be a highly prospective area. The most prospective areas for economic-grade minerals in the Okinawa Trough appear to be the JADE site and the SPOT area.  相似文献   

17.
In this study, we applied chemical geothermometers to the estimation of formation temperatures of chlorites from various types of hydrothermally altered rocks in the Toyoha geothermal field, using core samples from six drill holes (TH-2 to TH-7) together with wasted ore samples from Toyoha vein-type ore deposit. Based on the preliminary examination of mineral assemblages by X-ray powder diffraction and optical microscopy, hydrothermal alteration observed through the drill holes was classified into four types of alteration zones: propylitic, mixed-layer minerals, kaolin minerals, and ore mineralized zones. The mineral assemblage of the ore mineralized zone observed through TH-2, TH-4, and TH-6 is similar to those of Toyoha ore veins reported previously. The Fe3+/ΣFe ratios of chlorites were determined by X-ray photoelectron spectroscopy (XPS), in addition to the usual microprobe analyses. The ratios ranged from 0.20–0.26 for chlorites from the propylitic alteration zone and from 0.13 to 0.17 for those from the ore mineralized zone associated with sulfide minerals. After correcting the Fe3+ contents in the octahedral sites of chlorite structures, we obtained acceptable temperatures of the chlorite formation by application of geothermometers, for instance, a similar range of 150–300°C for chlorites from either the propylitic zone or the ore mineralized zone developed through TH-2, TH-4, and TH-6. Chlorites from the ore mineralized zone proximal to the Toyoha deposit are characterized by high Fe and Mn contents compared to the propylitic chlorites, which is similar to the Toyoha vein-filling chlorites; the formation temperatures were close to both the homogenization temperatures of fluid inclusions and the present subsurface temperatures measured through drill holes. Chlorites from the Toyoha ore veins, however, gave slightly higher formation temperatures (180–350°C) than those of chlorites from the ore mineralized zone in the drill cores. This suggests that several types of hydrothermal alteration occurred at different stages in the Toyoha geothermal field and the composition of product chlorite was controlled not only by the temperature but also the composition of fluid related to the formation. Reliable estimation of temperature for the chlorite formation provides basic information on evaluating correctly other physicochemical conditions prevalent at the formation.  相似文献   

18.
The Proterozoic Soldiers Cap Group, a product of two major magmatic rift phases separated by clastic sediment deposition, hosts mineralised (e.g. Pegmont Broken Hill‐type deposit) and barren iron oxide‐rich units at three main stratigraphic levels. Evaluation of detailed geological and geochemical features was carried out for one lens of an apatite‐garnet‐rich, laterally extensive (1.9 km) example, the Weatherly Creek iron‐formation, and it was placed in the context of reconnaissance studies of other similar units in the area. Chemical similarities with iron‐formations associated with Broken Hill‐type Pb–Zn deposit iron‐formations are demonstrated here. Concordant contact relationships, mineralogy, geochemical patterns and pre‐deformational alteration all indicate that the Soldiers Cap Group iron‐formations are mainly hydrothermal chemical sediments. Chondrite normalised REE patterns display positive Eu and negative Ce anomalisms, are consistent with components of both high‐temperature, reduced, hydrothermal fluid (≥250°C) and cool oxidised seawater. Major element data suggest a largely mafic provenance for montmorillonitic clays and other detritus during chemical sedimentation, consistent with westward erosion of Cover Sequence 2 volcanic rocks, rather than local mafic sources. Ni enrichment is most consistent with hydrogenous uptake by Mn‐oxides or carbonates. Temperatures inferred from REE data indicate that although they are not strongly enriched, base metals such as Pb and Zn are likely to have been transported and deposited prior to or following iron‐formation deposition. Most chemical sedimentation pre‐dated emplacement of the major mafic igneous sill complexes present in the upper part of the basin. Heating of deep basinal brines in a regional‐scale aquifer by deep‐seated mafic magma chambers is inferred to have driven development of hydrothermal fluids. Three major episodes of extension exhausted this aquifer, but were succeeded by a final climactic extensional phase, which produced widespread voluminous mafic volcanism. The lateral extent of the iron‐formations requires a depositional setting such as a sea‐floor metalliferous sediment blanket or series of brine pools, with iron‐formation deposition likely confined to much smaller fault‐fed areas surrounded by Fe–Mn–P–anomalous sediments. These relationships indicate that in such settings, major sulfide deposits and their associated chemical sediment marker horizons need not overlie major igneous sequences. Rather, the timing of expulsion of hydrothermal fluid reflects the interplay between deep‐seated heating, extension and magmatism.  相似文献   

19.
The Zhawulong granitic pegmatite lithium deposit is located in the Ganzi-Songpan orogenic belt. Fluid inclusions in spodumene and coexisting quartz were studied to understand the cooling path and evolution of fluid within albite–spodumene pegmatite. There are three distinguishable types of fluid inclusions: crystal-rich, CO2–NaCl–H2O, and NaCl–H2O. At more than 500°C and 350~480 MPa, crystal-rich fluid inclusions were captured during the pegmatitic magma-hydrothermal transition stage, characterized by a dense hydrous alkali borosilicate fluid with a carbonate component. Between 412°C and 278°C, CO2–NaCl–H2Ofluid inclusions developed in spodumene (I) and quartz (II) with a low salinity (3.3–11.9 wt%NaCl equivalent) and a high volatile content, which represent the boundary between the transition stage and the hydrothermal stage. The subsequentNaCl–H2Ofluid inclusions from the hydrothermal stage, between 189°C and 302°C, have a low salinity (1.1–13.9 wt%NaCl equivalent). The various types of fluid inclusions reveal the P–T conditions of pegmatite formation, which marks the transition process from magmatic to hydrothermal. The ore-forming fluids from the Zhawulong deposit have many of the same characteristics as those from the Jiajika lithium deposit. The ore-forming fluid provided not only materials for crystallization of rare metal minerals, such as spodumene and beryl, but also the ideal conditions forthe growth of ore minerals. Therefore, this area has favorable conditions for lithium enrichment and excellent prospecting potential.  相似文献   

20.
The Archean mafic–ultramafic complex of Lac des Iles, Ontario, Canada, hosts economic platinum group elements (PGE)-Au-Cu-Ni mineralization in the Roby Zone. All lithologies in the North Roby Zone have been affected by hydrothermal alteration. The alteration products include talc (the most dominant mineral), anthophyllite, serpentine, actinolite, tremolite, chlorite, hornblende, zoisite, clinozoisite, epidote and sericite. In the altered rocks, light rare earth elements (La, Ce, Nd, Sm), Pb, Rb, Ba, Cs, S and possibly Y have been added by hydrothermal solution whereas Eu and heavy rare earth elements (Yb, Gd, Dy, Er) remained immobile. There are five types of fluid inclusions in the pegmatitic plagioclase with homogenization temperature and salinity ranging from 240°C to 445°C and 15.37 to 48.52 wt% equivalent NaCl, respectively. The δ18O and δD of talc range form 6.2‰ to 6.9‰ and −28‰ to −48‰, respectively. δ18O and δD water in equilibrium with talc during the hydrothermal alteration suggest a modified source for the hydrothermal solution. Microthermometry and stable isotope studies suggest that high temperature–high salinity fluid was diluted by, and mixed with, low temperature–low salinity meteoric solution. This mechanism precipitated the hydrothermal assemblage and redistributed trace elements during and after pegmatite formation in the North Ruby Zone.  相似文献   

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